Recalls in June 2026 (page 2)
405 recalls.
- GE Healthcare MAC VU360 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported August 12, 2026 · Software issue issue with the MAC VU360 v3.0 system. After selecting the order refresh icon, an open preview or review screen might fail to close... - Merge OrthoPACS recall (Merge Healthcare, Inc.)
Medical deviceClass IIReported August 12, 2026 · Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open. - Merge PACS recall (Merge Healthcare, Inc.)
Medical deviceClass IIReported August 12, 2026 · Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open. - STRYKER PKG. recall (Stryker Corporation)
Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - STRYKER PKG. recall (Stryker Corporation)
Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING recall (Stryker Corporation)
Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - STRYKER AHTO TUBE SET WITH TIP PACKAGING recall (Stryker Corporation)
Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - STRYKER AHTO TUBE SET PACKAGING recall (Stryker Corporation)
Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 ... recall (Maquet Critical Care AB)
Medical deviceClass IIReported August 12, 2026 · Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient... - Brand Name: OXOS Medical recall (Oxos Medical Inc)
Medical deviceClass IIReported August 12, 2026 · Due to a defective circuit board that overheats - munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control... recall (MUNEVO GMBH)
Medical deviceClass IIReported August 12, 2026 · A software issue may cause the wheelchair's driving mechanism to fall out of calibration. When this occurs, the device may experience unexpected steering drift... - Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software... recall (Copan WASP)
Medical deviceClass IIReported August 12, 2026 · Due to a software issue within the WebApp that potentially prevents the user to overwrite the results. - Brand Name: Quantum Rehab Product Name: Quantum Rival Model/Catalog Number: Quantum... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: 4Front Model/Catalog Number: 4Front ... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Quantum 4Front 2HD Model/Catalog Number:... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Q6 Edge 4 Model/Catalog Number: Q6 Edge 4 ... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Model/Catalog Number: Q6 Edge 3 ... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Q6 Edge 2.0 recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Quantum 1450 Model/Catalog Number: Quantum... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum rehab Product Name: Q6 Edge 2.0 Model/Catalog Number: Q6 Edge... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Q6 Edge HD Model/Catalog Number: Q6 Edge HD ... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: R-TRAK Model/Catalog Number: R-TRAK ... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Stretto Model/Catalog Number: Q6... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Quantum Outback Model/Catalog Number:... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number:... recall (Pride Mobility Products Corp.)
Medical deviceClass IIReported August 12, 2026 · If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while... - Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN: Radial... recall (Boston Scientific Corporation)
Medical deviceClass IIReported August 12, 2026 · Potential for breach in sterile barrier of device packaging. - Radial Jaw 4 Large Capacity Biopsy Forceps with the following descriptions and UPN: ... recall (Boston Scientific Corporation)
Medical deviceClass IIReported August 12, 2026 · Potential for breach in sterile barrier of device packaging. - Radial Jaw 4 Standard Capacity Biopsy Forceps with the following descriptions and UPN:... recall (Boston Scientific Corporation)
Medical deviceClass IIReported August 12, 2026 · Potential for breach in sterile barrier of device packaging. - Charger for the Therabody Theragun recall (Therabody, Inc)
Medical deviceClass IIReported August 12, 2026 · Charging cradle for the device may overheat while charging the device's removable battery pack, presenting risk of thermal event (fire). Firm has received... - Requeson recall (Nelson & Isa Lacteos LLC)
FoodClass IReported August 5, 2026 · Products may be contaminated with Listeria monocytogenes. - AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Port Tray - RX recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported August 5, 2026 · Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices... - AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Loop Recorder... recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported August 5, 2026 · Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices... - AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Block Tray - RX recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported August 5, 2026 · Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices... - AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Heart Cath Tray - RX recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported August 5, 2026 · Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices... - AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Angio Pack - RX recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported August 5, 2026 · Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices... - AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Nerve Block... recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported August 5, 2026 · Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices... - AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Dr Fred Chiu... recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported August 5, 2026 · Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices... - AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: SPINAL KIT recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported August 5, 2026 · Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices... - EOPA 3D Arterial Cannula 22FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported August 5, 2026 · Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel... - EOPA 3D Arterial Cannula DIL TIP 22FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported August 5, 2026 · Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel... - EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported August 5, 2026 · Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel... - EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported August 5, 2026 · Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel... - EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported August 5, 2026 · Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel... - EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported August 5, 2026 · Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel... - L-Cath Midline S/L Catheter 20ga recall (Argon Medical Devices, Inc)
Medical deviceClass IIReported August 5, 2026 · Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may... - L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga recall (Argon Medical Devices, Inc)
Medical deviceClass IIReported August 5, 2026 · Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may... - AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Laminectomy Pack recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported August 5, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Neuro Pack recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported August 5, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported August 5, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported August 5, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides... recall (ResMed Ltd.)
Medical deviceClass IReported August 5, 2026 · Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of... - Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro CT5000 Ingenuity Premium ... recall (PHILIPS MEDICAL SYSTEMS)
Medical deviceClass IIReported August 5, 2026 · The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may... - IQon Spectral CT IQon Spectral CT Upgrades recall (PHILIPS MEDICAL SYSTEMS)
Medical deviceClass IIReported August 5, 2026 · The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may... - Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel ... recall (PHILIPS MEDICAL SYSTEMS)
Medical deviceClass IIReported August 5, 2026 · The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may... - Fusia recall (GELLERT GLOBAL GROUP)
FoodClass IReported July 29, 2026 · Undeclared Allergen (Fish) - 1. TNVitamins 100% Organic Moringa Capsules 1 recall (Total Nutrition Inc)
FoodClass IReported July 29, 2026 · Contaminated with Salmonella - Island Pacific IMITATION CRAB FLAKES recall (Shandong Ling Xian Food Co.,LTD)
FoodClass IIIReported July 29, 2026 · Undeclared sodium tripolyphosphate (STTP) - NAUTILUS IMITATION CRAB STICKS recall (Shandong Ling Xian Food Co.,LTD)
FoodClass IIIReported July 29, 2026 · Undeclared sodium tripolyphosphate (STTP) - Island Pacific IMITATION CRAB STICKS recall (Shandong Ling Xian Food Co.,LTD)
FoodClass IIIReported July 29, 2026 · Undeclared sodium tripolyphosphate (STTP) - Vintage Roots Root Beer Syrup recall (Vintage Roots LLC)
FoodClass IIReported July 29, 2026 · Unapproved food additive: sassafras bark. - Divalproex Sodium Delayed-Release Tablets recall (Bionpharma Inc.)
DrugClass IIReported July 29, 2026 · Presence of Foreign Tablets/Capsules - Dabigatran etexilate Capsules recall (Ascend Laboratories, LLC)
DrugClass IIIReported July 29, 2026 · Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and... - Dabigatran etexilate Capsules recall (Ascend Laboratories, LLC)
DrugClass IIIReported July 29, 2026 · Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and... - Cetirizine Hydrochloride Tablets USP 5 mg recall (JB Chemicals and Pharmaceuticals Ltd)
DrugClass IReported July 29, 2026 · Cross Contamination with Other Products: Customer complaints for appearance of discolored tablets and red dots observed on Cetirizine Hydrochloride Tablets... - Medline medical convenience kits labeled as: 1) TOTAL JOINT PACK Medline Kit SKU... recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of... - Medline medical convenience kits labeled as: NEURO PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of... - Medline medical convenience kits labeled as: 1) SHOULDER PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of... - Medline medical convenience kits labeled as: 1) KIT PEDIATRIC OPEN HEART MOSES recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - MiniMed Go App recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported July 29, 2026 · For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the... - Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 29, 2026 · Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases. - SnapshotGLO Wound Imaging Device recall (KENT IMAGING, INC.)
Medical deviceClass IIReported July 29, 2026 · The software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a battery that has fully discharged into... - Pipeline Flex Embolization Device with Shield Technology recall (Micro Therapeutics, Inc.)
Medical deviceClass IIReported July 29, 2026 · Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20... - Pipeline Flex Embolization Device with Shield Technology recall (Micro Therapeutics, Inc.)
Medical deviceClass IIReported July 29, 2026 · Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20... - Boston Scientific TheraSphere 360 Y-90 Management Platform recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Software anomaly occurs when a user adds one or more vials to the cart and subsequently returns to the Activity Calculator to modify one or more input. When a... - Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT recall (Penumbra, Inc.)
Medical deviceClass IIReported July 29, 2026 · Due to manufacturing issues, reperfusion catheters may fractures - Ventriculostomy Kit recall (Medtronic Neurosurgery)
Medical deviceClass IIReported July 29, 2026 · Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the... - MEDLINE medical procedure convenience kit labeled as: 1) TOTAL KNEE-LF recall (Medline Industries, LP)
Medical deviceClass IReported July 29, 2026 · The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to... - MEDLINE medical procedure convenience kit labeled as: HIP CDS-LF recall (Medline Industries, LP)
Medical deviceClass IReported July 29, 2026 · The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to... - Power F2 Powered Fastening System recall (Ferno-Washington Inc)
Medical deviceClass IIReported July 29, 2026 · Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case condition... - Hotline Fluid Warming Set recall (ICU Medical Inc.)
Medical deviceClass IIReported July 29, 2026 · ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent... - P28 PHANTON INTRAMEDULLARY NAIL SYSTEM recall (Paragon 28, Inc.)
Medical deviceClass IIReported July 29, 2026 · Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging. - FARADRIVE STEERABLE SHEATH CLEAR OUS recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to... - FARADRIVE STEERABLE SHEATH recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to... - FARADRIVE STEERABLE SHEATH CLEAR recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to... - FARADRIVE Steerable Sheath Clear IDE recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to... - FARASTAR Ablation Generator EU recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific is replacing specific FARASTAR PFA generators which have a configuration that is not compatible for use with the FARAPOINT PFA catheter. - FARASTAR PFA Generator recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information. - FARASTAR Pulsed Field Ablation Generator recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information. - FARASTAR Ablation Generator EU recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information. - MEDLINE convenience kits labeled as: 1) TOTAL JOINT KIT recall (Medline Industries, LP)
Medical deviceClass IReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose... - MEDLINE convenience kits labeled as: 1) C-SECTION recall (Medline Industries, LP)
Medical deviceClass IReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose...