Recalls in June 2026
405 recalls.
- Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack recall (Sarnova HC, Llc)
Medical deviceClass IIReported October 21, 2026 · Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula. - Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code:... recall (Micro Therapeutics, Inc.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect label/product dimensions. Product is supposed to be 3.00 mm in diameter, but unit is packaging was a 2.50 mm in diameter. - Products that contain the Pericare Wipes: recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray REF:... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: *Bardex¿ I.C. Complete Care¿ Foley Catheter... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray ... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Medline Convenience Kits: 1) BLOOD DRAW KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) ORTHO ASPIRATION KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) EYE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) C-SECTION PREP recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) LABOR CDS recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) PRE-OP KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) IV START KIT LAB DRAW-SH recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) ARTERIAL LINE INSERTION KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) IV START KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) ULTRASOUND BREAST PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) COLORECTAL ME recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) IVS BLOOD CULTURE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) DYKM1414 recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) CDS840396X recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Fresenius Medical Care recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 2, 2026 · Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ ... - American Contract System Convenience Kit recall (American Contract Systems Inc)
Medical deviceClass IIReported September 2, 2026 · The Convenience Kits contain Medline's Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has... - American Contract System Convenience Kits recall (American Contract Systems Inc)
Medical deviceClass IIReported September 2, 2026 · The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has... - American Contract System Convenience Kit recall (American Contract Systems Inc)
Medical deviceClass IIReported September 2, 2026 · The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has... - American Contract System Convenience Kit recall (American Contract Systems Inc)
Medical deviceClass IIReported September 2, 2026 · The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has... - Philips Incisive CT with software V4.5&V5.0 recall (Philips Healthcare (Suzhou) Co., Ltd.)
Medical deviceClass IIReported September 2, 2026 · Potential of failing to trigger clinical scan during Bolus Tracking. - Organic Whole Mixed Berries recall (Publix Super Markets, Inc.)
FoodClass IReported August 26, 2026 · Due to potential E. coli O145:H28 contamination - Organic Whole Mixed Berries recall (Publix Super Markets, Inc.)
FoodClass IReported August 26, 2026 · Due to potential E. coli O145:H28 contamination - Organic Whole Blueberries recall (Publix Super Markets, Inc.)
FoodClass IReported August 26, 2026 · Due to potential E. coli O145:H28 contamination - Organic Whole Blueberries recall (Publix Super Markets, Inc.)
FoodClass IReported August 26, 2026 · Due to potential E. coli O145:H28 contamination - Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard... recall (restor3d Inc.)
Medical deviceClass IIReported August 26, 2026 · Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws. - GETINGE Y SENSOR Module recall (Maquet Critical Care AB)
Medical deviceClass IIReported August 26, 2026 · The module did not undergo electrical safety tests and functional tests during production. - Arrow-LOK Implant recall (Arrowhead DE LLC)
Medical deviceClass IIReported August 26, 2026 · Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection. - One-Piece Guedel Airway recall (Intersurgical Inc)
Medical deviceClass IIReported August 26, 2026 · Devices could potentially be occluded or partially occluded. - One-Piece Guedel Airway recall (Intersurgical Inc)
Medical deviceClass IIReported August 26, 2026 · Devices could potentially be occluded or partially occluded. - Hamilton Microlab STAR Liquid Handler recall (Foundation Medicine, Inc.)
Medical deviceClass IIReported August 26, 2026 · Software issue that can cause an increase in spontaneous software closures. - 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 ... recall (BD SWITZERLAND SARL)
Medical deviceClass IIReported August 19, 2026 · Products may not have received adequate sterilization processing. - ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000 recall (Erbe USA Inc)
Medical deviceClass IIReported August 19, 2026 · A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector resulting in... - BIOFIRE Respiratory Panel 2.1 recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported August 19, 2026 · Due to increase in false negative results - GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. ... recall (Terumo Medical Corporation)
Medical deviceClass IIReported August 19, 2026 · Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire. - Allura Xper FD. Model Numbers: 722026 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported August 19, 2026 · Firmware issue potentially leading to loss of geometry movements. - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623 recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31... recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING ... recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 ... recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP recall (Galt Medical Corporation)
Medical deviceClass IIReported August 19, 2026 · Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits. - Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 ... recall (Spacelabs Healthcare, Inc.)
Medical deviceClass IIReported August 19, 2026 · Due to off-the-shelf display port component that has audio/video failures - Baxter Duo-Vent Solution Set and Male Luer Lock Adapter recall (Baxter Healthcare Corporation)
Medical deviceClass IReported August 19, 2026 · Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open... - Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF recall (CAMPO RICO FOODS LLC)
FoodClass IIIReported August 12, 2026 · Nitrofurans detected in product - Requeson recall (La Colonia Foods Llc)
FoodClass IReported August 12, 2026 · Products may be contaminated with Listeria monocytogenes. - Selectos Latinos Requeson Mexicano Mexican Cottage Cheese recall (La Colonia Foods Llc)
FoodClass IReported August 12, 2026 · Products may be contaminated with Listeria monocytogenes. - Selectos Latinos Requeson Salvadoreno Ricotta Style Salvadorean Cheese recall (La Colonia Foods Llc)
FoodClass IReported August 12, 2026 · Products may be contaminated with Listeria monocytogenes. - La Colonia Foods Salvadoreno Requeson Soft Ricotta recall (La Colonia Foods Llc)
FoodClass IReported August 12, 2026 · Products may be contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Clover Hill Dairy LLP recall (Clover Hill Dairy, LLC)
FoodClass IReported August 12, 2026 · Product contaminated with Listeria monocytogenes. - Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated... recall (Contego Medical, Inc)
Medical deviceClass IIReported August 12, 2026 · Carotid stent and post-dilation balloon system with integrated embolic protection system has an integrated filter, that due to a wire-to-filter-bond issue, may... - Blom-Singer Classic Indwelling Voice Prosthesis recall (Freudenberg Medical, LLC)
Medical deviceClass IIReported August 12, 2026 · Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large... - Blom-Singer Classic Indwelling Voice Prosthesis recall (Freudenberg Medical, LLC)
Medical deviceClass IIReported August 12, 2026 · Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Brand Name: COAPTIUM Connect Product Name: COAPTIUM Connect Model/Catalog Number:... recall (TISSIUM SA)
Medical deviceClass IIReported August 12, 2026 · Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use... - Philips Allura recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported August 12, 2026 · Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives. - Philips Azurion under the following System Descriptions and corresponding model... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported August 12, 2026 · Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives. - Philips Allura under the following System Descriptions and corresponding model... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported August 12, 2026 · Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives. - REF # D23354 recall (Beckman Coulter Inc.)
Medical deviceClass IIReported August 12, 2026 · Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications." - REF # D23352 recall (Beckman Coulter Inc.)
Medical deviceClass IIReported August 12, 2026 · Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications." - HardyDisk AST Cefiderocol 30¿g recall (Hardy Diagnostics)
Medical deviceClass IIReported August 12, 2026 · Due to incorrect cartridges include in affected products that there is the potential for false-susceptible or false-resistant susceptibility results and may... - Syva Emit tox Serum Tricyclic Antidepressant Calibrator/Controls SMN 10445390 ... recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIIReported August 12, 2026 · out-of-specification sodium azide concentration in Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2. While the assay results were not... - Syva Emit Disopyramide Assay Enzyme Immunoassay recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIIReported August 12, 2026 · Out-of-specification sodium azide concentration in Syva Emit Disopyramide Enzyme Immunoassay Calibrator Lot U1. While the assay results were not impacted, the... - INFINION CX LEAD KIT recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IReported August 12, 2026 · Spinal cord stimulation system lead body may be exposed to stress at the anchor site. This may result in high impedance measurements or lead fractures, which...