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
Baxter Healthcare is recalling 14,601 Novum IQ Syringe Pumps due to a software issue that may occur during multi-syringe infusions.
Ford is recalling 2026-2027 Transit vehicles because the rear seat belt reminder system may malfunction, failing to alert occupants if a seat belt is unfastened.
Philips is recalling Brilliance CT 64 systems due to an unintended radiation issue that could affect equipment performance.
Medline is recalling 3,752 Labor CDS and Vag Delivery Admission Bags due to packaging wrinkles that may compromise sterility, risking microbial contamination.
Medos International Sarl is recalling 29 Velys Robotic-Assist Stations due to a software issue that may cause unintended robotic arm movement during surgery.
Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could lead to infection.
Medline is recalling specific lots of convenience kits containing BD ChloraPrep applicators due to potential packaging seal defects that could allow contamination.
Philips is recalling IQon Spectral CT systems due to an unintended radiation issue that could affect equipment performance.
Baxter Healthcare is voluntarily recalling specific lots of Clindamycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators because packaging seals may be open or incomplete, posing a risk of infection.
Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could lead to infection.
Savor Seasonings LLC is recalling Organic Cheddar Type Seasoning because it tested positive for undeclared milk. The product was distributed to one consignee in Canada.
Medline is recalling specific lots of convenience kits containing BD ChloraPrep applicators due to potential packaging seal defects that could allow contamination.
Medline is recalling convenience kits containing BD ChloraPrep applicators due to potential packaging seal defects that could lead to infection.
Baxter Healthcare is voluntarily recalling specific lots of Vancomycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Baxter Healthcare is voluntarily recalling specific lots of Vasopressin in 0.9% Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Baxter Healthcare is voluntarily recalling specific lots of Clindamycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Baxter Healthcare is recalling four Novum IQ Syringe Pump loaner units due to a software issue that may occur during multi-syringe infusions.
Prince Bakery Inc is recalling 150 units of Italian and French bread in New York because sesame is not declared in the ingredient statement.
Medline is recalling 17,750 IVS Blood Culture Kits nationwide due to potential packaging defects that may compromise sterility.
Prince Bakery Inc is recalling 150 units of Pan De Manteca in New York because milk is not declared in the Contains statement.
Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could lead to infection.
AVID Medical, Inc. is recalling 11,763 Halyard medical convenience kits due to potential unexpected variability in endotoxin levels.
AVID Medical is recalling specific lots of Halyard medical convenience kits containing Ritmed Neurological Sponges due to potential endotoxin level variability.
Medline is recalling 434,595 convenience kits nationwide due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Medline is recalling 176 colorectal convenience kits due to potential packaging defects that may compromise sterility, posing a risk of microbial contamination.
Boston Scientific is recalling LUX-Dx Insertable Cardiac Monitor server software due to potential delays in Atrial Fibrillation Burden Alert notifications, which may delay clinical evaluation.
AVID Medical, Inc. is recalling specific lots of Ritmed Neurological Sponges Non-Sterile due to potential unexpected variability in endotoxin levels.
Prince Bakery Inc is recalling 150 units of Prince Italian Bread in New York because sesame is not declared in the ingredient statement.
Baxter Healthcare is voluntarily recalling MYXREDLIN insulin due to CGMP deviations. The recall covers specific lots distributed in the US, Puerto Rico, and Chile.
Prince Bakery Inc is recalling 150 units of Prince Sesame French Bread in New York because sesame is not declared in the ingredient statement.
Ford is recalling 2026 F-150 vehicles because stabilizer rod fasteners may not be tightened properly, which can cause the rod to shift and increase crash risk.
Baxter Healthcare is voluntarily recalling specific lots of CARDENE IV (Nicardipine Hydrochloride) injection due to CGMP deviations. The recall covers products distributed in the US, Puerto Rico, and Chile.
Medline is recalling blood culture kits containing BD ChloraPrep applicators due to potential packaging seal defects that could lead to infection.
Johnson & Johnson is recalling HEALON EndoCoat PRO and HEALON DUET PRO II viscoelastic products because surgical instructions may not adequately warn against forcing the cannula, which could cause eye injury.
Boston Scientific is recalling LUX-Dx Insertable Cardiac Monitor server software due to potential delays in Atrial Fibrillation Burden Alerts, which may delay clinical evaluation.
Medline is recalling specific lots of Cataract Preop Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could allow contamination.
Philips is recalling specific CT systems due to an unintended radiation issue that could affect equipment performance.
Fresenius Medical Care is recalling Granuflo Dry Acid Concentrate for hemodialysis due to complaints of blue-green discoloration in the product.
Medline is recalling 22,736 IV start kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Wonton Specialist is recalling 16 oz Lo Mein Noodles sold in New York, New Jersey, and Pennsylvania due to undeclared FD&C Red No. 40.
Baxter Healthcare is voluntarily recalling specific lots of Pantoprazole Sodium infusion bags due to Current Good Manufacturing Practice (CGMP) deviations.
Wonton Specialists is recalling 16 oz wonton skins sold in NY, NJ, and PA due to undeclared FD&C Red No. 40.
Mylan Pharmaceuticals is recalling Mycophenolate Mofetil for injection because it failed to meet dissolution specifications.
Mylan Pharmaceuticals is recalling 47,662 bottles of Prasugrel 10mg tablets because they failed dissolution specifications and 18-month stability testing.
Wonton Specialists is recalling 550 bags of Wonton Noodle in New York, New Jersey, and Pennsylvania due to undeclared FD&C Red No. 40.
Allies Group Inc. is recalling 29,014 tubes of THE ONE SPF 50 Invisible Sunscreen Gel because testing showed the product may not provide the labeled SPF 50 protection.
Lexia LLC is recalling Broadway Joe's Pain Cream in Colorado due to potential raw material contamination.
Cardinal Health 200, LLC is recalling 846 Presource Packs containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant, posing a risk of localized skin irritation.
Sage Products, LLC is recalling 165,536 packages of 2% Chlorhexidine Gluconate Cloth due to cross-contamination with other products.
Allies Group Inc. is recalling specific lots of THE ONE SPF 50 Invisible Sunscreen Gel because testing showed the product may not provide the labeled SPF 50 protection.
Cardinal Health is recalling 175 units of Presource Packs containing CliniClean Pericare Wipes due to potential lubricant contamination that may cause localized skin effects.
Cardinal Health is recalling Presource Packs containing CliniClean Pericare Wipes due to potential lubricant contamination that may cause localized skin effects.
Allies Group Inc. is recalling 2,149 tubes of SPF 50 sunscreen gel because testing showed it may not provide the labeled sun protection.
Lexia LLC is recalling Broadway Joe's Pain Cream in Colorado due to CGMP deviations and potential raw material contamination.
Cardinal Health is recalling specific urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Bionpharma Inc. is recalling Doxylamine Succinate and Pyridoxine HCl tablets because foreign tablets or capsules were found in the product.
Cardinal Health is recalling 60 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with manufacturing lubricant.
Cardinal Health is recalling 645 surgical kits containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Fresenius Medical Care is recalling Citrasate Liquid Acid Concentrate for Bicarbonate Hemodialysis due to complaints of blue-green discoloration.
Cardinal Health is recalling 61 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Cardinal Health 200, LLC is recalling 1,398 Presource Packs containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Cardinal Health is recalling 115 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with manufacturing lubricant.
Cardinal Health is recalling 19 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Cardinal Health is recalling 2,448 urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant, posing a risk of localized skin irritation.
Wonton Specialist is recalling 700 bags of cooked noodles in New York, New Jersey, and Pennsylvania due to undeclared FD&C Red No. 40.
Wonton Specialist Inc. is recalling 16 oz bags of Dumpling Skin due to undeclared FD&C Red No. 40. The product was distributed in New York, New Jersey, and Pennsylvania.
Cardinal Health is recalling 44 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Baxter Healthcare is voluntarily recalling Clindamycin Phosphate Injection due to Current Good Manufacturing Practice (CGMP) deviations. The affected product was distributed in the US, Puerto Rico, and Chile.
Diagnostica Stago is recalling 5,220 units of STA Staclot Protein S reagent because quality control values drifted within the stated stability period.
Allies Group Inc. is recalling 27,492 sachets of THE ONE SPF 50 Invisible Sunscreen Gel because firm testing indicated the product may not reliably provide the stated SPF 50 protection.
Fresenius Medical Care is recalling NaturaLyte Liquid Acid Concentrate for Bicarbonate Hemodialysis due to reports of blue-green discoloration in the product.
Chiesi USA is recalling 3,002 vials of Revcovi (elapegademase-lvlr) injection because the product failed stability specifications for protein concentration.
American Health Packaging is recalling 10,953 cartons of Buprenorphine Sublingual Tablets due to a label mix-up. The affected lot is distributed nationwide.
B Braun Medical Inc is recalling specific lots of Discofix Four Way Stopcock Extension Sets because the carton shipper labels display an incorrect expiration date.
Wonton Specialist Inc. is recalling Pan Fried Noodles due to undeclared FD&C Red No. 40. The product was distributed in New York, New Jersey, and Pennsylvania.
Supernus Pharmaceuticals is recalling Trokendi XR (topiramate) extended-release capsules because they failed dissolution specifications. The recall covers 11,304 bottles distributed nationwide.
Bombardier Recreational Products is recalling specific Can-Am motorcycles because the touchscreen instrument cluster may freeze or go blank, hiding critical safety information.
Prime Line Distributors and Ferrarini USA are recalling imported pork guanciale due to possible Listeria monocytogenes contamination found during routine testing.
Kibbi is recalling 2026-2027 Renegade recreational vehicles because a rooftop fan component may overheat and cause a fire.
Mondraker USA is recalling specific mountain bicycles equipped with ONOFF S9 Carbon MTB handlebars because they may crack or fracture, posing a risk of serious injury or death.
Nova Bus is recalling 2022-2024 LFS and LFS Artic buses because a faulty coolant sensor may cause unexpected engine shutdowns, increasing crash risk.
Audio Partnership is recalling Cambridge Audio Yoyo (M) Bluetooth speakers because their lithium-ion batteries can overheat and cause fires. No injuries have been reported.
Loyoda adult portable bed rails are being recalled because they violate safety standards, posing risks of entrapment, asphyxiation, falls, and lacerations.
Daikin Comfort Technologies is recalling Amana Through-The-Wall air conditioners and heat pumps because a shorted component can cause fire and serious injury.
Gizoon Direct is recalling six-drawer double dressers due to tip-over and entrapment risks that can cause serious injury or death to children.
Nanjing Wu Hai Smart Home Appliance Store is recalling Alanca 6-Drawer Dressers due to risks of serious injury or death from tip-over and entrapment.
Clorox is recalling about 6.3 million bottles of scented Mistolin and Lestoil cleaners sold in Puerto Rico and the U.S. Virgin Islands due to potential bacterial contamination.
Nova Bus is recalling Casco engine coolant level sensors that may send false signals, causing unexpected engine shutdowns and increasing crash risk.
Branch is recalling about 16,000 ergonomic chairs because the backrests can detach, posing a fall hazard. No injuries have been reported.
CPSC recalls GIHNJSI Squeezy Dumplings toys sold on Amazon due to water beads that pose serious ingestion, choking, and obstruction hazards.
OKK Trading is recalling Rainbow Mystery Squishy Bun Toys because water beads inside can expand and cause choking or intestinal obstruction if swallowed.
SHEIN is recalling about 963 Spiral Toys because they contain small balls that pose a choking hazard to children under three.
Skip Hop is recalling Baby Sesame Street Elmo Silicone Teethers because the black eyes can detach if frozen, posing a choking risk.
Truststone Group is recalling XO Poppy Power Trip Magnetic Wireless Power Banks because the lithium-ion batteries can overheat and ignite, posing fire and burn risks.
KHONG GUAN (HQ) is recalling Glutinous Rice Balls with Black Sesame Filling due to undeclared peanuts. The product was distributed in eight US states.
Sirna & Sons Produce is recalling 249 bags of 1 lb jalapeno peppers due to potential Salmonella Javiana contamination. The product was distributed for food service use in Ohio and Pennsylvania.
Jaime's Foods ATX, LLC is recalling Jalapeno Ranch in 16 oz. glass jars because the product contains an undeclared egg allergen. The recall affects 102 cases distributed in Texas.
ZMB Enterprises is recalling Addall XR Shot liquid dietary supplements because they contain undeclared ingredients 1,4-DMAA, Phenylethylamine, and Phenibut.
Mallinckrodt is recalling ACTHAR Gel vials due to the presence of glass and stopper pieces. Patients should stop using the product and contact their healthcare provider.
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