Archive
593 recalls were announced in September 2026.
Of the 593 recalls this month scored against our rubric, 7% are Critical, 32% are Severe.
Which agencies issued them
AVID Medical is recalling Halyard IV Start Kits because they contain applicators potentially contaminated with Aspergillus penicillioides.
Evergreen Fresh Sprouts LLC is recalling broccoli sprouts in Washington due to a potential Salmonella contamination risk.
GIAS FOOD INC. is recalling Bettergoods Lemon Alfredo Fettuccine due to Listeria monocytogenes contamination. Consumers should stop eating the product and return it to Walmart.
Sterling Pharmaceutical Services LLC is recalling specific lots of Cameron Pharmaceuticals Carboxymethylcellulose Sodium 0.5% Eye Lubricant due to a lack of assurance of sterility.
CooperSurgical is recalling specific lots of INCA Infant Nasal CPAP tubing because a loose connection may cause loss of pressure and reduced oxygenation.
Sterling Pharmaceutical Services LLC is recalling Walgreens Lubricant Eye Drops due to a lack of assurance of sterility. The recall affects 199,600 packs distributed nationwide.
Grech is recalling 2026-2027 Strada, Terreno, and Turismo motorhomes because a rooftop ventilation fan circuit board may overheat and cause a fire.
Highland Ridge RV is recalling 2022-2024 Range Lite Air travel trailers because fastener failure may cause the fresh water tank to detach, creating a road hazard.
Whole Foods Market is recalling Cabricharme cheese sold in several states due to an undeclared egg allergen. Consumers should check their refrigerators and discard or return the product.
Sterling Pharmaceutical Services is recalling Sodium Chloride Hypertonicity Ophthalmic Solution, 5%, due to a lack of assurance of sterility.
Sterling Pharmaceutical Services LLC is recalling specific lots of Lubricating Tears because the company cannot guarantee the product is sterile.
Sterling Pharmaceutical Services LLC is recalling Gentle Eyes Lubricant Eye Drops due to a lack of assurance of sterility.
Sterling Pharmaceutical Services LLC is recalling Major LubriFresh P.M. Nighttime Ointment due to a lack of assurance of sterility. The recall covers 34,368 tubes distributed nationwide.
United Sugar Producers and Refiners is recalling specific batches of United and Good & Gather light brown sugar due to potential wheat kernel contamination.
Sterling Pharmaceutical Services LLC is recalling AvKare Carboxymethylcellulose Sodium Ophthalmic Solution due to a lack of assurance of sterility.
Medline Industries is recalling 128 Major Pack Convenience Kits containing neurological sponges due to potential endotoxin variability that may cause adverse health events.
Olympus is recalling 404 BiCOAG Hemostasis Probes because the ceramic tip may detach due to insufficient adhesive.
Sterling Pharmaceutical Services LLC is recalling AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% due to a lack of assurance of sterility.
Insight Pharmaceuticals is recalling 2.3 million bottles of Clear Eyes Redness Relief eye drops due to a lack of assurance of sterility.
Insight Pharmaceuticals is recalling specific lots of Clear Eyes Redness Relief eye drops due to a lack of assurance of sterility.
Sterling Pharmaceutical Services LLC is recalling Walgreens Lubricant Eye Drops due to a lack of assurance of sterility. Consumers should stop using the product.
Volkswagen is recalling 2023-2026 ID.4 vehicles because the high voltage battery may fail and cause a vehicle fire, increasing the risk of injury.
Boston Scientific is recalling Imager II Angiographic Catheters because the tip may fracture or detach, potentially causing device fragments to remain in or migrate through the patient's vasculature.
CooperSurgical is recalling 149 boxes of INCA Neonatal Nasal CPAP replacement sets because the flexible tubing may disconnect from the nasal cannula, potentially reducing treatment effectiveness.
Medline is recalling Healthmark Instrument Channel Brush kits due to potential sharp edges that could cause cuts, abrasions, or infection.
Olympus is recalling 105 BiCOAG Hemostasis Probes because a manufacturing defect may cause the ceramic tip to detach during use.
Olympus Corporation of the Americas is recalling 816 units of BiCOAG Hemostasis Probes because the ceramic tip may detach due to insufficient adhesive.
Philips is recalling 219 EPIQ Elite Diagnostic Ultrasound Systems due to a software issue that may cause inaccurate blood flow velocity measurements and potential misdiagnosis.
Becton, Dickinson and Company is recalling 15,455 ForeSight Elite Tissue Oximetry Cables due to incorrect switching of Channel 1 and 2 on the module and flag labels.
Heidelberg Engineering is recalling 87 SPECTRALIS units with Flex Modules because wheels may detach, causing the stand to tip over and injure nearby people.
Maquet is recalling 667 PowerLED 300 Concealed Lighting Systems because the spring arm may detach and fall, posing a potential injury risk.
Abiomed is recalling 3,322 Automated Impella Controllers worldwide due to firmware and software defects that affect pressure signal accuracy and system reliability.
Medline is recalling Healthmark Instrument Channel Brush kits due to potential sharp edges that could cause cuts, abrasions, or infection.
Midmark Corporation is recalling 20 IQvitals Zone units because a performance issue may cause inaccurate blood pressure readings when using the Linear Deflation Method.
Elegant Foods, LLC is recalling Pecorino Toscano D.O.P. STAGIONATO cheese wheels in Wisconsin due to potential Listeria contamination from cooler condensation.
Medline is recalling 234 neurological surgery kits nationwide due to potential endotoxin variability that may cause adverse health reactions.
Midmark Corporation is recalling 33 IQvitals Zone units because a performance issue may cause inaccurate blood pressure readings when using the Linear Deflation Method.
New York Embroidery Studio is recalling 5,400 Trinity Non-Surgical Isolation Gowns because they do not consistently meet minimum liquid-barrier performance requirements.
Cardinal Health is recalling 17,503 Presource Convenience Kits because applicator packaging may have open or incomplete seals, posing a risk of infection.
Olympus is recalling 2,142 BiCOAG Hemostasis Probes because a manufacturing error may cause the ceramic tip to detach.
Greenpower is recalling 94 EV Star buses because a software error may allow the vehicle to move while the wheelchair lift is deployed.
Midmark Corporation is recalling 153 IQvitals Zone units because a performance issue may cause inaccurate blood pressure readings when using the Linear Deflation Method.
SeaSpine Orthopedics is recalling 270 units of the Mariner Deformity Extended Polyaxial Head because the proximal thread depth is out of design specification.
Intervascular is recalling Cardioroot Woven Collagen Coated Vascular Grafts because the product failed to meet acceptance criteria for Integral Water Permeability.
United Sugar Producers and Refiners is recalling specific batches of powdered sugar due to potential wheat kernel contamination. The product was distributed in eight states.
Medline is recalling 486 craniotomy convenience kits due to potential endotoxin variability that may cause adverse health reactions.
Biomerieux Inc is recalling VITEK 2 AST-N461 test kits due to card pouch damage that may cause false resistant results, potentially leading to less effective antibiotic treatments.
Midmark Corporation is recalling IQvitals Zone devices because a performance issue may cause inaccurate blood pressure readings when using the Linear Deflation Method.
Medline is recalling 695 convenience kits containing neurological sponges due to potential endotoxin variability that may cause adverse health reactions.
Amneal Pharmaceuticals is recalling 5,694 Exenatide Injection pens because the delivery system may be defective, potentially leaving the pen empty of medication.
Shantou Qiwei Industrial Co., Ltd is voluntarily recalling 2,970 units of MENOW Sunscreen Pressed Powder SPF35 PA+++ in California due to cGMP deviations.
Medline Industries is recalling 4,013 neurological surgery kits due to potential endotoxin variability that may cause adverse health reactions.
Cardinal Health 200, LLC is recalling Presource Convenience Kits because applicator packaging may have open or incomplete seals, posing a risk of infection.
Starcraft RV is recalling 2022-2024 Super Lite Maxx travel trailers because fasteners may fail, causing the fresh water tank to detach and create a road hazard.
Philips is recalling 387 Achieva 1.5T MRI systems worldwide because a software issue may terminate examinations if manual scan adjustments exceed system memory.
Ventec Life Systems is recalling 25 HomeFill Oxygen Systems because the cylinders lack required medical gas labeling.
Baxter Healthcare is recalling six PRO+ 40-inch MRS Surface mattresses due to errors in the Unique Device Identification (UDI) label text.
Criticare Technologies is recalling 1,007 nGenuity Patient Monitors because a setup error renders the CO2 monitoring function inoperable, potentially delaying procedures.
Baxter Healthcare is recalling two VOLARA systems because contamination in test equipment may have affected flow rate accuracy. Affected devices were returned and confirmed to meet specifications.
DeRoyal Industries is recalling Myocardial Probes that contain an 18mm needle instead of the specified 15mm needle.
Philips is recalling 611 MR 5300 MRI scanners due to a software issue that can terminate examinations during image reconstruction if system memory is exceeded.
Philips is recalling Ingenia 3.0T and 3.0T CX MRI systems because a software issue can terminate examinations during image reconstruction if scan parameters exceed available system memory.
Fresenius Medical Care is recalling CombiSet Hemodialysis Blood Tubing Sets to ensure treatment preparation and handling steps are performed as instructed.
Philips is recalling 91 MRI systems due to a software issue that can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.
Philips is recalling 922 Ingenia Ambition MRI systems due to a software issue that can terminate examinations if system memory is exceeded.
CooperVision is recalling specific lots of Pearle Vision 1 Day contact lenses because a small number of lenses have the incorrect power.
Ventec Life Systems is recalling two HomeFill Oxygen Systems because the cylinders lack required medical gas labeling.
Philips is recalling 37 MR 7700 MRI systems due to a software issue that can terminate examinations during image reconstruction.
Philips is recalling 210 Achieva 3.0T MRI scanners because a software issue can terminate examinations if system memory is exceeded during image reconstruction.
Baxter Healthcare is recalling 169 PRO+ MRS Mattresses because UDI label errors may lead to incorrect product identification or use with incompatible bed frames.
Philips is recalling 82 Intera 1.5T MRI systems worldwide because a software issue can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.
Olympus is recalling 305 units of EZDilate Endoscopic Balloon Dilators because the inflation chart label may incorrectly indicate balloon diameters of 18, 19, or 20 mm.
Philips is recalling 2,038 Ingenia 1.5T MRI systems worldwide due to a software issue that can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.
Baxter Healthcare is recalling 824 PRO+ 36-inch MRS Surface mattresses due to errors in the Unique Device Identification (UDI) label. The discrepancies may lead to incorrect product identification or use with incompatible bed frames.
AVID Medical is recalling 192 Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.
Kwok Shing, Inc. is recalling 70 boxes of American Ginseng due to potential pesticide contamination. The product was distributed in California.
Philips is recalling SmartPath MRI software due to a defect that can terminate examinations during image reconstruction if system memory is exceeded.
Philips is recalling 15 Achieva XR MRI systems because a software issue can terminate examinations if scan parameters exceed system memory.
Philips is recalling 596 Ingenia Elition MRI systems due to a software issue that can terminate examinations during image reconstruction if system memory is exceeded.
WWF Operating Company is recalling So Delicious Dairy Free Salted Caramel Cluster Cashewmilk because it may contain small stones and other hard objects.
AVID Medical is recalling Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.
Ventec Life Systems is recalling 21 HomeFill Oxygen System cylinders because they lack required medical gas labeling.
Macleods Pharmaceuticals is recalling Olanzapine 5 mg tablets because organic and unspecified impurities exceeded specifications.
Chrysler is recalling MOPAR body and jumper wiring harnesses because water intrusion can disable electric power steering assist, increasing crash risk.
Rivian is recalling 2027 R2 vehicles because a high voltage battery fastener may be improperly tightened, which can cause a loss of drive power and increase crash risk.
Chrysler is recalling 2026 Ram 1500 vehicles because side air bag connectors may not be secured properly, potentially preventing deployment in a crash.
Chrysler is recalling 2026 Ram 1500 vehicles because tire pressure sensors may fail to detect low pressure or illuminate the warning light, increasing crash risk.
Nova Bus is recalling 2022-2023 LFS transit buses because short mounting screws may cause the bike rack to detach, creating a road hazard.
Chrysler is recalling 2022-2026 Ram Promaster and 2024-2026 Ram 3500 Electric vehicles because water may enter the steering wiring harness, potentially disabling power steering assist.
Mack Trucks is recalling 850 Anthem and Pioneer vehicles due to software errors that may reduce braking performance when hauling tanker trailers.
Volvo Trucks North America is recalling 2025-2027 VNL and 2026-2027 VNR trucks with tanker packages due to inaccurate axle load calculations that may reduce braking performance.
Cummins is recalling L9 diesel engines because remote fuel filter hoses may separate, causing fuel leaks, engine stalls, and increased fire or crash risks.
Sempio Food Services is recalling ready-to-eat chicken stew products imported from Korea without required reinspection. No illnesses have been reported.
Fontanini Foods is recalling raw, frozen pork sausage links that may contain clear, hard plastic. The products were distributed to food service establishments in four states.
ATC is recalling 2024-2026 RM900 and 2026 RM700 trailers because coupler mounting bolts may loosen, potentially separating the coupler and increasing crash risk.
INMO International Technology Limited is recalling INMO Air3 Smart Glasses because the left temple can overheat, posing a risk of serious injury or death from burns.
ABC Trading is recalling light-up glasses, headbands, and ties because accessible button cell batteries pose a risk of serious injury or death if swallowed.
Grand Design is recalling 2024-2027 Reflection fifth wheel trailers because a solar controller may output incorrect voltage, risking fire or brake failure.
NEWDERY is recalling ZHX-PB22 power banks sold on Amazon due to fire and burn hazards. The lithium-ion batteries can explode or ignite, posing a risk of serious injury.
The Blue Cactus Company is recalling 2500 mAh battery packs for reclining chairs due to fire and burn hazards. CPSC is aware of four reports of overheating, smoking, or ignition.
Looking for a different month? Back to 2026.