Archive
661 recalls were announced in October 2026.
Of the 661 recalls this month scored against our rubric, 2% are Critical, 31% are Severe.
Which agencies issued them
NOXBOX LTD is recalling 1,667 NOxBOXi Nitric Oxide Delivery Systems due to a manufacturing issue that may cause irregular oxygen readings.
Percussionaire Corporation is recalling 98,434 In-Line Valves to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.
Heraeus Medical is recalling PALACOS MV+G pro 40 and 80 bone cement due to potential monomer liquid leakage. The recall affects 20,523 units distributed worldwide.
Wright Medical Technology is recalling 34 Charlotte Claw Screws because missing threads on the screwheads may prevent secure engagement with the plate, potentially prolonging surgery.
American Nitrile Operations LLC is recalling 36.8 million Opportunity Flex blue nitrile gloves due to defects like tears and debris that may expose users to pathogens or chemicals.
TOJI CO. is recalling Cloud Cafe Collagen Milk due to an undeclared fish allergen. The product was sold to a single distributor in Los Angeles.
SV Labs Toronto Corporation is recalling specific lots of Benzoyl Peroxide Wash, USP, 5% due to microbial contamination. The product was distributed in Illinois.
Cardinal Health 200, LLC is recalling 2,957 gynecological laparoscopy kits because the handpieces may leak fluid, creating a slip and fall hazard.
Cardinal Health 200, LLC is recalling 22 Presource Packs containing Stryker StrykeFlow PS and AHTO tube sets because the handpieces may leak fluid, creating a slip and fall hazard.
American Contract Systems Inc. is recalling medical convenience kits containing BD CliniClean Pericare Wipes due to potential lubricant contamination.
Shanghai United Imaging Healthcare is recalling 11 uCT ATLAS CT systems due to a software issue that may hide patient images, potentially requiring rescans.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, while the correct validated shelf life is 5 years.
TerSera Therapeutics is recalling 296 cartons of Zoladex (goserelin) implants because the product sat in a non-temperature-controlled trailer for 25.5 hours.
ASP Global is recalling 6,100 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling 240 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling MPR Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is only 5 years.
ASP Global, LLC. is recalling 1,899 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the validated shelf life is 5 years.
SLT Foods Inc. is recalling Khazana Fennel Candy due to undeclared food dyes Yellow 5, Yellow 6, Red 3, and Blue 1.
ASP Global, LLC. is recalling 70 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is only 5 years.
Shanghai United Imaging Healthcare is recalling six uMI Panvivo S PET/CT systems due to a software defect that may hide patient images, potentially requiring rescans.
ASP Global, LLC. is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling 850 sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling 1,692 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling 396 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling 40 units of MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling MPR Single Use Tourniquet Cuffs because the expiration dates are incorrect. The products are labeled with a 10-year shelf life, but the validated shelf life is 5 years.
Shanghai United Imaging Healthcare is recalling 23 uCT 550 CT systems due to a software issue that may hide patient images, potentially requiring rescans.
Philips is recalling six Ingenia Blue Seal MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate tractography reconstruction.
ASP Global, LLC. is recalling MPR Disposable Tourniquet Cuffs because the expiration date is incorrect. The product is labeled with a 10-year shelf life, but the validated shelf life is 5 years.
ASP Global, LLC. is recalling 4,530 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
ASP Global is recalling MPR single-use tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life, while the validated shelf life is 5 years.
ASP Global is recalling 4,850 sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Philips is recalling Ingenia Ambition S and X MRI systems because diffusion tensor imaging (DTI) exports contain incorrect data, preventing correct processing by third-party software.
ASP Global, LLC. is recalling 2,600 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life, while the correct validated shelf life is 5 years.
Custom Interventional Pain Management is recalling 56 units of Mastisol Skin Adhesive trays due to manufacturing issues with the liquid skin adhesive.
ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Shanghai United Imaging Healthcare is recalling seven uMI Panorama 35 PET/CT systems due to a software issue that may hide patient images, potentially requiring rescans.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Olympus Corporation of the Americas is recalling 72 units of the M3 Gold Autoclavable Foroblique Telescope 30 due to discrepancies between sterilization parameters in the Instructions for Use and the Japanese package insert.
Shanghai United Imaging Healthcare is recalling 14 uCT 780 CT systems due to a software defect that may hide patient images, potentially requiring rescans.
ASP Global, LLC. is recalling 30 units of MPR Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
ASP Global is recalling Expressaire Disposable Tourniquet Cuffs because the expiration date is incorrect. The product is labeled with a 10-year shelf life, but the validated shelf life is 5 years.
ASP Global, LLC. is recalling 260 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
ASP Global, LLC. is recalling 970 MPR single-use tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling Expressaire Disposable BB Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
Percussionaire Corporation is recalling 61,858 units of IPV 1 and Phasitron 5 breathing circuits to update labeling warnings regarding use with volatile anesthetic delivery systems.
ASP Global is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because the expiration dates are incorrect. The products are labeled with a 10-year shelf life, but the validated shelf life is 5 years.
Shanghai United Imaging Healthcare is recalling one uCT 760 CT system due to a software defect that may hide patient images, potentially requiring rescans.
Shanghai United Imaging Healthcare is recalling 53 uCT ATLAS Astound CT systems due to a software defect that may hide patient images, potentially requiring rescans.
Philips is recalling Upgrade dStream software versions R11-R13 because DTI scan exports contain incorrect diffusion direction data, preventing correct tractography reconstruction.
ASP Global, LLC. is recalling 156 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Percussionaire Corporation is recalling 419 Intrapulmonary Percussive Ventilation (IPV) devices to update labeling warnings regarding the use of volatile anesthetic delivery systems.
Amneal Pharmaceuticals is recalling 2,592 cartons of Estradiol Gel 0.1% because some packets were found to be empty or partially full.
Illumina is recalling 80 NovaSeq 6000Dx and DRAGEN Server units worldwide due to a security vulnerability in the server component.
ASP Global is recalling 6,510 sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Percussionaire Corporation is recalling IPV-1C and Phasitron 5 devices to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.
ASP Global is recalling Expressaire disposable tourniquet cuffs due to incorrect expiration dates. The products were labeled with a 10-year shelf life, but the validated shelf life is 5 years.
Philips is recalling five SmartPath to MR 7700 units because diffusion tensor imaging exports contain incorrect data, preventing correct processing by third-party software.
Alere San Diego is recalling multiple hCG urine test strips because they may detect low hCG levels, resulting in false positive results.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Beckman Coulter is recalling AU480 Chemistry Analyzers because a software error prevents the instrument from starting, delaying patient results.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Olympus is recalling 50 units of the M3 Gold Autoclavable Lateral Telescope 70 in Japan due to discrepancies between sterilization parameters in the Instructions for Use and the Japanese package insert.
ASP Global, LLC. is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is 5 years.
Shanghai United Imaging Healthcare is recalling one uMI 780 PET/CT system due to a software defect that may hide patient images, potentially requiring rescans.
ASP Global is recalling 360 MPR single-use tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Ajanta Pharma USA Inc. is recalling Ranolazine Extended-Release Tablets, 1000 mg, because the product failed to meet dissolution specifications.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
Shanghai United Imaging Healthcare is recalling three uMI Panorama GS PET/CT systems due to a software issue that may hide patient images, potentially requiring rescans.
Philips North America is recalling 131 MR 5300 systems because diffusion tensor imaging exports contain incorrect data, preventing accurate tractography reconstruction.
Alere San Diego, Inc. is recalling multiple hCG pregnancy test models because they may detect low hCG levels, resulting in false positive results.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
Philips is recalling SmartPath MRI software because it exports incorrect diffusion tensor imaging data, preventing correct processing by third-party tractography software.
Philips is recalling 340 Ingenia MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate third-party processing.
Shanghai United Imaging Healthcare is recalling three uMI Panvivo PET/CT systems due to a software issue that may hide patient images, potentially requiring rescans.
ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Philips is recalling Ingenia 1.5T MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate processing by third-party software.
ASP Global, LLC. is recalling 36 units of Expressaire Disposable BB Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling 400 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Olympus is recalling 543 DisplayPort cables used with the OLYSENSE Hub System because they may cause video dropouts or blackouts during high-power operation.
ASP Global, LLC. is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Admiral Beverage Corporation is recalling 7up Tropical beverage cans labeled as Zero Sugar that actually contain full sugar. The recall covers 3,240 cases distributed to Utah.
ASP Global, LLC. is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
Percussionaire Corporation is recalling IPV-2C and Phasitron 5 devices to update labeling warnings regarding the use of these devices with volatile anesthetic delivery systems.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
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