Sterility problems recalls
732 recalls.
- Baby Brezza Enterprises Recalls SuperFast Sterilizer Dryers Due to Overheating and Burn Hazards
Consumer productReported November 5, 2026 · The recalled sterilizer dryers can overheat when plugged in and operating, posing a risk of injury from a burn hazard if the surface is handled. - Sunny Sky Non-Dairy French Vanilla Creamer recall (Sunny Sky Products, LLC)
FoodClass IIReported November 4, 2026 · Product sterility was potentially compromised. - Vecuronium Bromide for Injection recall (Meitheal Pharmaceuticals, Inc)
DrugClass IIIReported November 4, 2026 · Labeling: Label Lacks Warning or Rx Legend - Vecuronium Bromide for Injection recall (Meitheal Pharmaceuticals, Inc)
DrugClass IIIReported November 4, 2026 · Labeling: Label Lacks Warning or Rx Legend - OXYTOCIN recall (Eagle Pharma Outsourcing LLC)
DrugClass IIReported November 4, 2026 · Lack of Assurance of Sterility - PHENYLephrine HCL Infusion recall (Eagle Pharma Outsourcing LLC)
DrugClass IIReported November 4, 2026 · Lack of Assurance of Sterility - Carboxymethylcellulose Sodium recall (Huons Co., Ltd.)
DrugClass IIReported November 4, 2026 · Failed Impurities/Degradation Specification; detection of polyethylene (PE)-related oligomers - PENTAX Medical Water bottle assembly. Model Number. OS-H5. recall (Pentax of America Inc)
Medical deviceClass IIReported November 4, 2026 · Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during... - PENTAX Medical Ultrasound Endoscope. Model Number. EG-3270UK. recall (Pentax of America Inc)
Medical deviceClass IIReported November 4, 2026 · Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during... - PENTAX Medical Ultrasound Endoscope. Model Numbers. EG-3870UTK recall (Pentax of America Inc)
Medical deviceClass IIReported November 4, 2026 · Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during... - PENTAX Medical Ultrasound Endoscope. Model Numbers. EG38-J10UT recall (Pentax of America Inc)
Medical deviceClass IIReported November 4, 2026 · Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during... - PENTAX Medical Ultrasound Endoscope. Model Number. EG36-J10UR. recall (Pentax of America Inc)
Medical deviceClass IIReported November 4, 2026 · Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during... - Glutathione Injection recall (Greenwich Rx)
DrugClass IReported October 28, 2026 · Microbial Contamination of Sterile Products - Testosterone Cypionate recall (Right Value Drug Stores LLC)
DrugClass IIReported October 28, 2026 · Lack of sterility assurance. - Heparin Sodium Injection recall (Shenzhen Techdow Pharmaceutical Co., Ltd.)
DrugClass IIReported October 28, 2026 · Lack of Assurance of Sterility - Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH30. recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 28, 2026 · A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications. - Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH31. recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 28, 2026 · A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications. - Generic Name: restor3d MTP Implant Generic Name: MTP Implant Model/Catalog Number:... recall (restor3d Inc.)
Medical deviceClass IIReported October 28, 2026 · Implants were found in the field with orange sterilzation indicators which means implants were not exposed to sterilization. - Medtronic Biopsy Needle Kit recall (Medtronic Navigation, Inc.)
Medical deviceClass IIReported October 28, 2026 · Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect... - Medtronic NDI Passive Spheres REF: 8801075 recall (Medtronic Navigation, Inc.)
Medical deviceClass IIReported October 28, 2026 · Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect... - Medtronic NDI Passive Spheres REF: 8801074 recall (Medtronic Navigation, Inc.)
Medical deviceClass IIReported October 28, 2026 · Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect... - Medtronic NDI Passive Spheres REF: 8801071 recall (Medtronic Navigation, Inc.)
Medical deviceClass IIReported October 28, 2026 · Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect... - Sermorelin recall (Houston Rx LLC)
DrugClass IIReported October 21, 2026 · Lack of process control - Tirzepatide/Niacinamide 2mL vial recall (Houston Rx LLC)
DrugClass IIReported October 21, 2026 · Lack of assurance of sterility. - Vinyl Instrument Guards recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported October 21, 2026 · Labeling not compliant with 21 CFR 801 and steam sterilization IFU has been updated. - Scout MD recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported October 21, 2026 · The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use. - TS Misc. Instruments Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - Triathlon Hinge Femoral Prep Tray. Catalog Number: 6543-6-514. recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - TS Femoral Prep Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - TS Universal Baseplate Finishing Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture recall (Ethicon, LLC)
Medical deviceClass IIReported October 21, 2026 · Silk sutures, indicated for use in cardiovascular, ophthalmic and neurological procedures, packaged with alcohol-based fluid, not part of product design, that... - FORWARD Gunshot Wound Kit recall (INTEGRATED MEDCRAFT LLC)
Medical deviceClass IIReported October 21, 2026 · Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the... - iFuse TORQ Implant System Model/Catalog Number: 10055T recall (SI-BONE, Inc.)
Medical deviceClass IIReported October 21, 2026 · The pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be ensured. - Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined... recall (Medtronic Sofamor Danek USA Inc)
Medical deviceClass IIReported October 21, 2026 · Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to... - Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined... recall (Medtronic Sofamor Danek USA Inc)
Medical deviceClass IIReported October 21, 2026 · Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related... - Tri-Immune Boost recall (Centric Compounding LLC)
DrugNot Yet ClassifiedReported October 14, 2026 · Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin. - Apothecary NAD+ Injection 200 mg/mL recall (Apothecary Pharma LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Tirzepatide Injection recall (Apothecary Pharma LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - TIRZEPATIDE/CYANOCOBALAMIN 85/2 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - TIRZEPATIDE/CYANOCOBALAMIN 76/2 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - TIRZEPATIDE/CYANOCOBALAMIN 64/2 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - TIRZEPATIDE/CYANOCOBALAMIN 26/2 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - SEMAGLUTIDE/CYANOCOBALAMIN 9/2 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to processing equipment used in compounded product. - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to processing equipment used in compounded product. - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to processing equipment used in compounded product. - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to processing equipment used in compounded product. - QUAD-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to processing equipment used in compounded product. - SERMORELIN ACETATE 1 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - SEMAGLUTIDE/CYANOCOBALAMIN 3/2 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - SEMAGLUTIDE 3 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - TIRZEPATIDE 26 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - Sterile High Performance Ultra Lubricating Eye Drops recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Sterile Eye Drops Redness Relief recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Sterile Eye Drops recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Sterile Lubricant Dry Eye Relief Eye Drops recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Eye Drops MAXIMUM recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Sterile EYE DROPS Advanced Relief recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Sterile EYE DROPS AC recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Artificial Tears Sterile Lubricant Eye Drops recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - BARD EP XT DECAPOLAR STEERABLE recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported October 14, 2026 · Diagnostic electrophysiology (EP) catheter may have a breached sterile barrier on the straight seal side of the primary pouch, which if used could lead to... - VERIFY Biological Steam Test Pack Model/Catalog Number: S3069 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Biological Steam Test Pack Model/Catalog Number: S3065 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - FOCUS PI Hypromellose 0.7% Formula recall (Aurolab Trust)
DrugClass IIReported October 7, 2026 · Lack of Assurance of Sterility - Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger... recall (SPECTRUM MEDICAL SRL)
Medical deviceClass IIReported October 7, 2026 · Due to blood-to-glycol leak in the heat exchanger. - Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger... recall (SPECTRUM MEDICAL SRL)
Medical deviceClass IIReported October 7, 2026 · Due to blood-to-glycol leak in the heat exchanger. - Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported October 7, 2026 · Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the... - Olympus M3 Gold Autoclavable Lateral Telescope 70. Model Number: M3-70A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported October 7, 2026 · There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the... - Olympus M3 Gold Autoclavable Foroblique Telescope 30. Model Number: M3-30A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported October 7, 2026 · There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the... - Brand Name: Ferndale Laboratories recall (Custom Interventional Pain Management, LLC)
Medical deviceClass IIReported October 7, 2026 · Due to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits. - Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 18" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15" 1 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 12" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 12" 1 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 8" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44" 1 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 34" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 34" 1 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 30" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 30" 1 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 24" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 24" 1 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 18" 1 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 26" DUAL BLADDER recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 20" DUAL BLADDER recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 20" DUAL BLADDER recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct...