Medical device recalls (page 22)
2545 recalls.
- Medline kits containing Tego Connectors Medline APHERESIS SUBQPORT ACCESS KIT SKU... recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Convenience kits used for dialysis maintenance Medline ADD A CATH DIALYSIS KIT SKU... recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Medline Kits containing Tego Connectors Medline DIALYSIS ON/OFF KIT SKU EBSI1746 recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Medline Kits containing Tego Connectors: Medline IR Pack recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - PIE PAK Models: P2HC-A recall (Edermy LLC)
Medical deviceClass IIReported March 4, 2026 · Lack of 510K clearance - PIE Trolley System Model: 2005 recall (Edermy LLC)
Medical deviceClass IIReported March 4, 2026 · Lack of 510K clearance - Brand Name: Reverse Shoulder Prosthesis recall (Encore Medical, LP)
Medical deviceClass IIReported March 4, 2026 · Knee and Humeral socket implants contain incorrect labeling. - Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS recall (Encore Medical, LP)
Medical deviceClass IIReported March 4, 2026 · Knee and Humeral socket implants contain incorrect labeling. - Brand Name: Reverse Shoulder Prosthesis recall (Encore Medical, LP)
Medical deviceClass IIReported March 4, 2026 · Knee and Humeral socket implants contain incorrect labeling. - Meijer STERILE saline wound wash recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Medline Convenience Kits: 1) NAIL KIT recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Medline Convenience Kits: 1) NAIL KIT recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Medline Sterile Saline Wound Wash recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR recall (Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha)
Medical deviceClass IIReported March 4, 2026 · Software anomaly in the patient positioning system may result in positional discrepancy. - Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR recall (Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha)
Medical deviceClass IIReported March 4, 2026 · Software anomaly in the patient positioning system may result in positional discrepancy. - Da Vinci 5 ASSY recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported February 25, 2026 · An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or... - MOLLI 2 System System includes: MM1000 recall (Stryker Corporation)
Medical deviceClass IIReported February 25, 2026 · Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target... - Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software... recall (Centinel Spine, Inc.)
Medical deviceClass IIReported February 25, 2026 · Products were mislabeled as the 6mm product but included the 5 mm product. - Medline Surgical Packs: 1) PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Surgical Gowns: 1) GOWN recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Surgical Drapes: 1) SHEET recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ARTHROSCOPY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) SPINAL CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT OPHTHALMIC RUPTURE GLOBE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BAP NORTH ROBOTIC SURGERY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) HYSTEROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) C-SECTION PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT UROLOGY SLING recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ROBOTIC GYN CDS-1 recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OB KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) NEURO SHUNT- CODMAN recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CHEST/BREAST-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LVAD DRIVELINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ADMIT KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAPE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PPE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAPE PACK-CHOICE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT GENERAL CLOSURE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BURN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) WMC I D PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LVAD DRIVELINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT ACES INSERT PEG recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) TOTE ABRAMS KNEE ARTHROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAWER 6-IV FLUIDS GLOVES recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LITHOTOMY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BAPTIST FLOYD ENDO GI KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) MAJOR LAPAROTOMY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CHP COCHLEAR SUPPLEMENT CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DENTAL PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PICC LINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OR ARTERIOGRAM recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ENDO KIT W/SYRINGE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BASIC NERVE BLOCK TRAY W/LINEN recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) SCC RF PAIN MGMT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT STC TRACHEOSTOMY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ANCILLARY PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - MONARCH Platform recall (Auris Health, Inc)
Medical deviceClass IIReported February 25, 2026 · Device for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope... - Medica Capillary Tubes recall (Medica Corporation)
Medical deviceClass IIReported February 25, 2026 · A systematic positive bias of up to 20% was identified across the reportable potassium range, resulting in false elevation results of patient samples when... - Estrone RIA recall (Immunotech A.S.)
Medical deviceClass IIReported February 25, 2026 · The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability. Only in some (very... - Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 ... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported February 25, 2026 · Pumps were released without full testing being performed, including occlusion alarm testing. - Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth... recall (Bard Peripheral Vascular Inc)
Medical deviceClass IIReported February 25, 2026 · Due to damage to outer tray that can potentially compromise the sterile barrier - Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and... - Private Label CVS. Model Number: CVS405406. Helps maintain a moist wound environment recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY. Model Numbers: recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - Teslatome Bipolar Sphincterotomes REF: TESLA-B2535-260 Model Number: G60784 UDI-DI... recall (Wilson-Cook Medical Inc.)
Medical deviceClass IIReported February 25, 2026 · Due to product that may contain a void in the material that separates the wire guide and cutting wire lumens, which may cause an inappropriate path of current... - Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflation of... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - da Vinci 5 Surgeon Console Viewer Display recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported February 18, 2026 · Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth... - Azurion 5 M20 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 5 M12 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 7 M20 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 7 M12 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 7 B20 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 7 B12 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 3 M15 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 3 M12 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - ATEC Lateral Navigation Disc Prep Instruments LIF NAV recall (Alphatec Spine, Inc.)
Medical deviceClass IIReported February 18, 2026 · Due a design issue where the navigated array connection geometry is incorrect. - ATEC Lateral Navigation Disc Prep Instruments LIF NAV recall (Alphatec Spine, Inc.)
Medical deviceClass IIReported February 18, 2026 · Due a design issue where the navigated array connection geometry is incorrect. - Laerdal Compact Suction Unit 4 RTCA version recall (Laerdal Medical Corporation)
Medical deviceClass IIReported February 18, 2026 · units manufactured in a limited time period may emit electromagnetic noise beyond the acceptable limits for RTCA application specified in RTCA DO-160G Chapter... - Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system... recall (Elekta, Inc.)
Medical deviceClass IIReported February 18, 2026 · Due to an error when defining a new stereotactic reference that users fail to first change an already defined obsolete reference to a pre-plan reference. This... - Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system... recall (Elekta, Inc.)
Medical deviceClass IIReported February 18, 2026 · Due to an error when defining a new stereotactic reference that users fail to first change an already defined obsolete reference to a pre-plan reference. This... - Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01. recall (AVID Medical, Inc.)
Medical deviceClass IIReported February 18, 2026 · Tyvek bag seal issue which may compromise sterility of the kit. - WB Impression Post Closed Tray incl. guide screw recall (Straumann USA LLC)
Medical deviceClass IIIReported February 18, 2026 · The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown. - Medline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 18, 2026 · Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may... - Medline medical convenience kits packaged as: STERILE RESUTURE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 18, 2026 · Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may... - Medline medical convenience kits packaged as: ) LVAD DRESSING CHANGE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 18, 2026 · Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may... - Medline medical convenience kits packaged as: BLOOD CULTURE KIT NS recall (Medline Industries, LP)
Medical deviceClass IIReported February 18, 2026 · Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may... - Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 18, 2026 · Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may... - Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING CHANGE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 18, 2026 · Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may... - 1) UNIVERSAL KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 18, 2026 · Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may... - Medline medical convenience kits packaged as: 1) CANCER SERVICE PORT KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 18, 2026 · Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may... - Medline medical convenience kits packaged as: PEDIATRIC CATH SECUREMENT DRSG recall (Medline Industries, LP)
Medical deviceClass IIReported February 18, 2026 · Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may... - Medline medical convenience kits packaged as: ADULT CATH SECUREMENT DRSG recall (Medline Industries, LP)
Medical deviceClass IIReported February 18, 2026 · Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may...