Archive
497 recalls were announced in September 2026.
Of the 497 recalls this month scored against our rubric, 8% are Critical, 29% are Severe.
Which agencies issued them
restor3d Inc. is recalling two Kinos Axiom Total Ankle Systems because they were packaged with incorrect patient-specific cutting guides, which may lead to surgical complications.
Taylor Fresh Foods is recalling diced jalapenos due to potential Salmonella contamination. The product was distributed in multiple US states.
Taylor Fresh Foods is recalling 13-ounce Authentic Guacamole products in 27 states due to potential Salmonella contamination.
Elegant Foods, LLC is voluntarily recalling 5-pound bags of Golden Raisins in Wisconsin due to undeclared sulfites.
Elegant Foods LLC is recalling 5-pound bags of Coconut Flakes in Wisconsin due to undeclared sulfites.
Forest River is recalling 2025-2026 Cedar Creek fifth wheel trailers because a sleeper sofa may block the bunkroom door, potentially delaying emergency exits.
ICU Medical is recalling IV sets with drip chambers because black specks may be present in the fluid path due to a plastic molding issue.
Stryker is recalling XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.
Best Friends Bakery is recalling 1,416 units of Pumpkin Spice No Bake Cookies due to peanut and egg labeling errors.
Medline is recalling 135 Open Heart A Pack kits in California due to a potential sterile barrier breach in the RCSP cannulae, posing a risk of infection.
GE Healthcare is recalling 116 Centricity PACS Server V7 systems because historical imaging data may be incorrectly associated with the wrong patient, potentially leading to misdiagnosis.
BD Switzerland is recalling BD Alaris Pump Infusion Sets due to discrepancies in performance data that may lead to inappropriate pump performance.
Philips North America is recalling 7,359 Patient Information Center iX units due to a software malfunction that may cause the system to freeze and become unresponsive.
Nuclein LLC is recalling 182 DASH Rapid PCR Instruments due to a software issue. The recall affects units distributed in 18 US states.
Medline Industries is recalling 341 anesthesia pain kits due to open sterile seals that may compromise sterility and lead to patient infection.
ICU Medical is recalling IV sets with drip chambers due to potential black specks and particulate matter in the fluid path.
ICU Medical is recalling Plum administration sets because drip chambers may contain black specks or discolored PVC material. The presence of particulate matter in the fluid path has not been ruled out.
Panorama Produce Sales Inc. is recalling Martina brand Fresh Whole Mangoes due to potential Salmonella contamination. The product was distributed in Connecticut, New York, New Jersey, and Pennsylvania.
Abiomed is recalling 1,422 Impella Optical Controllers because a purge flag component may fail, causing purge cassette recognition issues.
Maquet Cardiopulmonary GmbH is recalling Percutaneous Insertion Kits because packaging may not consistently maintain sterile barrier integrity.
ICU Medical is recalling IV sets with drip chambers due to potential black specks and particulate matter in the fluid path.
Medical Action Industries is recalling blood culture kits containing BD ChloraPrep applicators with potentially compromised sterile seals, posing a risk of localized skin infection.
Stryker is recalling 9,072 XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.
Maquet is recalling Percutaneous Insertion Kits because the packaging may not consistently maintain sterile barrier integrity.
Howmedica Osteonics Corp. is recalling specific Scorpio knee implant components due to aged polyethylene material that may cause increased wear and potential device failure.
Medline Industries is recalling 459 units of Minor Pack convenience kits because open sterile seals may compromise sterility and lead to patient infection.
GE Healthcare is recalling Core Services Hub V8 software because historical imaging data may be incorrectly associated with the wrong patient, potentially leading to misdiagnosis.
Beak & Skiff Sanitizer Alcohol Antiseptic 80% is being recalled because FDA analysis found acetaldehyde above specification limits in the product. The recall affects bottles distributed in New York and through online sales.
Quality Dairy Farms Inc. is recalling Mercer's brand ice cream sandwiches in New York due to undeclared peanuts.
GE Healthcare is recalling Enterprise Archive V8 software because historical imaging data may be incorrectly associated with different patients, potentially leading to misdiagnosis.
Nova Biomedical is recalling StatStrip Glucose and B-Ketone meters because a software defect may cause patient data to be assigned to the wrong medical record.
Howmedica Osteonics Corp. is recalling specific orthopaedic implant components made from aged polyethylene. The material may oxidize and wear excessively, potentially causing device failure.
Forest River is recalling 2026-2027 Dynamax Isata recreational vehicles because the bunk ladder may loosen if attached to a wooden mattress insert, increasing injury risk.
Howmedica is recalling specific orthopaedic implant components made with aged UHMWPE material that may oxidize, potentially leading to increased wear and device failure.
Happiest Baby, Inc. is recalling SNOO Sleep Sacks because they have not been reviewed for safety and effectiveness by the FDA.
Stryker is recalling XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.
NOXBOX LTD is recalling 1,547 NOxBOXi Nitric Oxide Delivery Systems due to potential oxygen tubing leaks that may cause oxygen desaturation.
Embecta Medical II LLC is recalling Nano Pro Un-Cannulated Demo Samples because investigational-use-only pen needles were inadvertently distributed as commercially marketed devices.
Taylor Fresh Foods Inc is recalling BH Bold Chef Salad Kits due to potential Salmonella contamination. The products were distributed in 28 U.S. states.
GE Healthcare is recalling Workflow Core Services V8 because historical imaging data may be incorrectly associated with the wrong patient, potentially leading to misdiagnosis.
Medline Industries is recalling 60 Myringotomy Pack-LF kits due to open seals that may compromise sterility and lead to patient infection.
ICU Medical is recalling 185,688 CADD Yellow Medication Cassette Reservoirs because they may leak medication at the connector joint, potentially interrupting therapy or causing exposure to harmful agents.
Forest River is recalling 2026-2027 Dynamax Isata recreational vehicles because a misaligned bunk mat may not be supported, increasing the risk of occupant injury.
Howmedica is recalling Triathlon hinge inserts made with aged polyethylene that may wear excessively, potentially causing device fracture or the need for revision surgery.
Buckhead Meat Company is recalling specific lots of tuna due to high levels of scombrotoxin detected by the NJ Department of Health.
Maquet is recalling Percutaneous Insertion Kits because the packaging may not consistently maintain sterile barrier integrity, posing a risk of infection.
Boston Scientific is recalling StoneSmart Connect Console power adapters that may fail electrical safety testing due to high grounding resistance.
ICU Medical is recalling 107,800 oncology sets because drip chambers may contain black specks from the molding process, which could lead to product replacement and therapy delays.
Abiomed is recalling 5,232 Automated Impella Controllers because a purge flag component may fail, causing recognition issues.
Taro Pharmaceuticals is recalling Lidocaine Ointment 5% due to failed content uniformity specifications during stability testing.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product is distributed nationwide.
Inventia Healthcare Limited is recalling 13,567 bottles of Chlorthalidone 25 mg tablets because they failed dissolution specifications. The recall is nationwide.
ICU Medical is recalling 28,550 oncology sets because drip chambers may contain black specks from the molding process. The discolored material does not enter the fluid path but may cause therapy delays.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product was distributed nationwide.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product is distributed nationwide in the USA.
Safecor Health is recalling Fluphenazine HCl Elixir because it failed stability specifications. The product was distributed nationwide in the USA.
Elegant Foods is recalling Carrot Cakes because the carrot decorations contain Yellow #5 and Yellow #6, which are not listed on the product label.
Tiffany Food Corp is recalling Hexing Haw Balls candy because it contains the unapproved dye Ponceau 4R.
F & A Foundation is recalling 600 units of Reign Medical Clench Staple Systems because the device's performance characteristics have not been adequately established.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product was distributed nationwide.
ICU Medical is recalling IV Non-Dedicated Gravity Administration Sets because black specks in the drip chamber may cause healthcare providers to delay therapy.
Straumann USA LLC is recalling 216 GM Helix Implants because the packaging identification does not match the actual implant dimensions.
Embecta Medical II LLC is recalling pen needles labeled 'For Investigational Use Only' that were inadvertently distributed as commercially marketed devices.
Safecor Health is recalling Fluphenazine HCl Elixir because it failed stability specifications. The product is distributed nationwide.
Well Lead Medical Co. Ltd is recalling SunMed Tracheal Tubes because a 6Fr suction catheter could not pass through the samples smoothly.
Abiomed is recalling Impella Optical Controllers because a purge flag component may fail, causing recognition issues. The recall covers 4,100 units distributed in the US and internationally.
Wilson-Cook Medical Inc. is recalling 121,241 units of Hemospray Endoscopic Hemostat due to issues with endoscope adherence and the inability to spray powder.
Nova Bus is recalling 2024-2025 LFS transit buses because an improperly tightened emergency brake valve may cause air leaks and unintentional parking brake activation.
Ford is recalling 2024-2026 Ranger vehicles with 10.1-inch center stack screens that may lose power and fail to display the rearview camera image, increasing crash risk.
Ford is recalling 2026 Ranger vehicles because the center screen may lose power, preventing the rearview camera image from displaying and increasing crash risk.
Star Meat Delivery Inc. is recalling raw pork, beef, and goat products produced without federal inspection and bearing false USDA marks.
Forest River is recalling 2026-2027 Dynamax Grand Sport GT recreational vehicles because an improperly installed engine pre-heat pump may cause coolant hose failure and engine overheating.
REV is recalling specific 2025-2027 recreational vehicles because the RoadWatch Safety System may have incorrect programming, potentially disabling safety features.
Volvo Bus is recalling 2009-2025 9700 buses because the emergency exit label on the entrance door is missing operating instructions, which may delay evacuation.
Winnebago is recalling 2027 Arka recreational vehicles because the rear Gross Axle Weight Rating and tire inflation data on the federal placard are incorrect.
Sauna360 is recalling infrared and hybrid saunas because panels can short circuit and overheat, posing fire and burn risks.
Jaguar Land Rover is recalling specific 2019-2024 models because a DC-DC converter malfunction can cause loss of drive power and lighting, increasing crash risk.
LANCHEZ pressure washers are recalled because they lack a ground-fault circuit-interrupter and adequate power cord, posing risks of shock or electrocution.
Tongyang Cycling is recalling Basecamp bicycle helmets because they violate mandatory safety standards, posing a risk of serious head injury or death.
Regfear is recalling BedsPick mattresses because they violate mandatory flammability standards, posing a risk of serious injury or death from fire.
Toyota is recalling 617 specific 2026 Lexus and Toyota models because front steering knuckles may crack, potentially causing a loss of steering control.
JKMAX is recalling about 195,000 heated blankets and heating pads because internal wires can overheat, posing fire and burn risks.
Sauna360 is expanding a recall of Tylö Halmstad and Kiruna Hybrid Saunas because the benches can collapse, posing a fall hazard to users.
Hayward Industries is recalling 400,000 BTU Universal-HC Series pool heaters because they can produce high levels of carbon monoxide, posing a risk of serious injury or death.
Colerinsec is recalling Jerify Magnetic Humanoid Toy Sets because loose magnets can be swallowed, posing a risk of serious injury or death to children.
Friedrich is recalling about 2,000 Kühl Q and S window air conditioners because a control board failure can cause fire and burn hazards.
Toyworld168 is recalling Rainbow Mystery Squishy Bun Toys because water beads inside can expand and cause choking or intestinal obstruction if swallowed.
Esjay is recalling toddler busy board toys because red knobs can detach, posing a choking hazard to children under three.
Melissa & Doug is recalling about 84,000 Lights & Sounds Fire Truck Activity Board toys sold at Target and Amazon because a fire hose port can detach, posing a choking risk.
SHEIN is recalling Pull & Chew Montessori Teething Toys because the silicone strings violate safety standards and pose a choking risk. No injuries have been reported.
Char-Broil is recalling about 10,605 Bistro Pro Electric Grills because a grounding wire can disconnect, posing an electric shock hazard. No injuries have been reported.
B. Braun Medical Inc. is recalling 0.9% Sodium Chloride Injection due to the presence of particulate matter, including iron oxide and fibers.
American Regent, Inc. is recalling 31,935 vials of Epinephrine Injection due to the presence of particulate matter and broken vials.
Exotique Foods Canada is recalling Momchipz Gluten Free Veggie Chips due to undeclared wheat. The product was sold in the U.S. and poses a risk to individuals with wheat allergies.
Medical Action Industries is recalling Single Shot Epidural kits containing Sodium Chloride ampules due to potentially compromised sterility.
Nipro Renal Solutions is recalling Citric Complete Dry Citric Acid Concentrate due to high endotoxin levels. The product is used in hemodialysis.
Euro Foods Group USA NJ Inc is recalling Crown Farms Dried Suri Cut because the dried fish was not properly eviscerated prior to drying.
Nipro Renal Solutions is recalling MedicaLyte Liquid Bicarbonate Concentrate due to high endotoxin levels. The product is used in hemodialysis.
Nipro Renal Solutions is recalling Citric Complete Liquid Citric Acid Concentrate due to high endotoxin levels. The product was distributed in the US and internationally.
Baxter Healthcare is recalling 606 bags of Dextrose Injection, USP, 70% due to the presence of stainless steel particles in the solution.
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