Archive
417 recalls were announced in March 2026.
Of the 417 recalls this month scored against our rubric, 0% are Critical, 20% are Severe.
Which agencies issued them
Terex is recalling 2019-2026 digger utility trucks because a weld defect may cause the pole guide arm to fall, posing an injury risk.
General Motors is recalling 2018-2019 Chevrolet and GMC trucks because roof rail air bag inflators may rupture, posing an injury risk.
Amazon is recalling the Amazon Basics Camping Folding Pocket Knife because the folding mechanism can fail to remain properly secured in the closed position, posing a laceration hazard.
Specialized is recalling bicycle forks on all Turbo Como SL electric bicycles because the fork steerer tube can develop a small fatigue crack leading to progressive failure of the fork.
Goregent infant walkers are being recalled because they can fit through a standard doorway and fail to stop at the edge of a step, violating the mandatory standard for infant walkers.
Lifetime Brands is recalling BUILT LUUM light up tumblers because they can break, making the button cell batteries accessible to children and posing choking and ingestion hazards.
Tainoki Fine Furniture is recalling Noah, Owen and Warren swivel office chairs because the chair base can bend, posing a fall hazard.
Hyundai is recalling certain 2026 Palisade and Palisade Hybrid vehicles with Limited and Calligraphy trim packages due to damaged wiring in the third-row driver-side seat belt buckle that may prevent the warning indicator from alerting to unfastened belts.
Made Fresh Salads brand Vegetable Cream Cheese in 5 lb tubs is being recalled due to potential Listeria monocytogenes contamination. Affected products have expiration dates through February 27, 2026.
Made Fresh Salads brand Garlic & Herb Cream Cheese (5 lb tubs) is being recalled because it may be contaminated with Listeria monocytogenes. The affected product was distributed in New York.
Made Fresh Salads brand Scallion Cream Cheese in 5 lb tubs is being recalled because the product may be contaminated with Listeria monocytogenes. All expiration dates through 2/27/2026 are affected.
Made Fresh Salads brand Lox Cream Cheese (5 lb tubs) is recalled due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX PRO blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Made Fresh Salads brand Walnut Raisin Cream Cheese in 5 lb tubs is being recalled because it may be contaminated with Listeria monocytogenes. The recall affects products distributed in New York with expiration dates through 2/27/2026.
Made Fresh Salads brand Jalapeno Cream Cheese in 5 lb tubs is being recalled due to potential Listeria monocytogenes contamination. All products with expiration dates through February 27, 2026 sold in New York are affected.
Made Fresh Salads brand Caramel Apple Cream Cheese in 5 lb tubs is being recalled because it may be contaminated with Listeria monocytogenes. The recall affects product distributed in New York with expiration dates through February 27, 2026.
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX GO blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Made Fresh Salads brand Strawberry Cream Cheese in 5 lb tubs is being recalled due to potential Listeria monocytogenes contamination. The product was distributed in New York.
Made Fresh Salads brand Sundried Tomato Cream Cheese (5 lb tubs) is being recalled because it may be contaminated with Listeria monocytogenes. Consumers should not eat the product and should contact the manufacturer or their retailer.
Made Fresh Salads brand Tofu Whipped in 5 lb tubs is being recalled because products may be contaminated with Listeria monocytogenes. The recalled product was distributed in New York.
Made Fresh Salads brand Whipped Cream Cheese in 5 lb tubs is being recalled due to potential contamination with Listeria monocytogenes. The product was distributed in New York.
Made Fresh Salads brand Jalapeno Cheddar Cream Cheese in 5 lb tubs is recalled due to potential Listeria monocytogenes contamination. The product was distributed in New York.
Made Fresh Salads brand Apple Cinnamon Cream Cheese in 5 lb tubs is being recalled because the product may be contaminated with Listeria monocytogenes. The recall affects products distributed in New York with all expiration dates through 2/27/2026.
Made Fresh Salads brand Blueberry Cream Cheese (5 lb tubs) sold in New York is being recalled due to potential contamination with Listeria monocytogenes. The FDA classifies this as a Class I recall.
Ambrosia Brands LLC is recalling Rosabella brand Moringa dietary supplement capsules nationwide and internationally because the product may be contaminated with Salmonella.
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX AIR blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Lutronic is recalling the CLARITY II Laser System after reports of devices sparking or popping and potentially burning patients.
Medline is recalling five surgical drape products because the fabric may delaminate prematurely when the included laundering instructions are followed.
Covidien is recalling the HealthCast Vital Sync Remote Patient Monitoring System after complaints that alarms from the primary patient bedside monitor were not transmitted to or received by the remote system.
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8521/15 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Instrumentation Laboratory is recalling GEM Premier 5000 analyzers after confirmed complaints that GEM PAK cartridges may show increased Process Control Solution Not Detected errors during warm-up.
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/05 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Raz Design is recalling several Mobile Shower Commode Chair models because a vendor modification means the seat may be reinstalled without properly engaging the outside rear seat brackets that hold it in place.
Beckman Coulter is recalling Chemistry Analyzer AU5800 units because leaving the calibration monitor open beyond 15 minutes can trigger database errors that stop the system analyzing.
CNC Noodle Corporation is recalling ZHONG HUA CHAO MIAN fresh noodles due to undeclared wheat and Yellow #6 food coloring on the label. Consumers with wheat allergies or sensitivities to the colorant may be at risk.
Coco's Italian Market Cannoli Making Kit is recalled because the label lists flour and ricotta cheese as sub-ingredients but fails to declare wheat and milk allergens. Consumers with wheat or milk allergies may be at risk if they consume the product.
Toyota is recalling certain 2022–2026 Lexus NX, RX, and TX vehicles because the rearview camera image may fail to display when the vehicle is in reverse, reducing rear visibility and increasing crash risk.
Jaguar Land Rover North America is recalling certain 2026 Land Rover Defender vehicles because the third-row lower seat belt anchorage bracket may have an insufficient weld stud, potentially preventing proper restraint during a crash.
Keystone is recalling certain 2026 Montana fifth wheel trailers because improperly secured 12-volt and 120-volt wiring may be pinched and damaged when the bedroom slide-out moves, increasing fire risk.
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415008 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360008 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Instrumentation Laboratory is recalling GEM Premier 5000 parts 00055445010 and 00055445011 after confirmed complaints of Process Control Solution Not Detected errors during warm-up.
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-2836/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055445004 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Coco's Italian Market Heat-n-Eat Fettuccini Alfredo is recalled because the label lists semolina and durum flour as sub-ingredients but does not declare wheat. Consumers with wheat allergies or sensitivities may be at risk.
Exactech is recalling the Equinoxe Core Instrument Kit, model KIT-311X, because the impactor handle may be missing a cross-pin.
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8030/12 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Medline is recalling Medcrest surgical gowns because the fabric may delaminate prematurely when the included laundering instructions are followed.
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055407510 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415005 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415011 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-2835/12 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8521/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055430004 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055445008 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055415004 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055407504 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415010 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/15 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055430011 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/12 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Physio-Control is recalling Infant/Child Reduced Energy Defibrillator Electrodes, catalogue numbers 11101-000016 and 11101-000017, due to pediatric defibrillator electrode delamination.
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055407511 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055407508 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Zydus Pharmaceuticals is recalling eight lots of Icosapent Ethyl Capsules 1 gram after red dots and melted capsules were found, caused by oxidation of the active ingredient.
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/07 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/16 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Exactech is recalling the Equinoxe Ergo Modular Impactor Handle, model 321-09-05, because the impactor handle may be missing a cross-pin.
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream (3 gallon tubs) is being recalled because it contains undeclared egg, a common allergen. The recall affects 4,880 tubs distributed in Illinois.
Polski Ogrod Sp. z o.o. is recalling Hortex Mieszanka 9 Spring vegetable mix due to potential glass contamination. The affected product was distributed in Illinois.
Willamette Valley Pie Company is recalling frozen raw blueberry crumble pies due to potential listeria monocytogenes contamination. The pies were distributed to grocery store in-store bakeries in Illinois and Oregon.
CNC Noodle Corporation is recalling China Noodle Co. Steam Noodle packages due to undeclared wheat in the product, which poses a risk to consumers with wheat allergies.
Willamette Valley Pie Company is recalling Frozen Raw Bulk 9 inch Blueberry Crumble Pie due to potential contamination with listeria monocytogenes. The frozen pies were sold to grocery retailers' in-store bakeries in Illinois and Oregon.
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360011 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
International Life Sciences is recalling Artelon FlexBand Plus, refs 41054 and 41057, because the augmentation devices failed bacterial endotoxin testing.
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360004 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/02 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
International Life Sciences is recalling the Artelon FlexBand Twist .12, ref TW012, because the augmentation devices failed bacterial endotoxin testing.
Ion Beam Applications is recalling PROTEUS 235 proton therapy systems because a disabled interface means the safety system may not interrupt beam delivery if the external gating signal is lost.
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055430008 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360010 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Beckman Coulter is recalling DxC 700 AU analyzers because leaving the calibration monitor open beyond 15 minutes can trigger database errors that stop the system analyzing.
Palmetto Gourmet Foods Inc. is recalling Vegetarian Chicken Flavor Ramen Express because the product contains undeclared Yellow #5 food coloring, a major allergen for some consumers.
International Life Sciences is recalling the Artelon FlexBand Dynamic Matrix, ref 31057, because the augmentation devices failed bacterial endotoxin testing.
Boston Scientific is recalling EndoVive Safety PEG Kits containing BD ChloraPrep Triple Swabsticks because open or compromised seals on the swabstick packaging could cause loss of sterility.
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8521/09 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Ford is recalling certain 2022-2025 Lincoln Navigator, Nautilus, Aviator and Explorer vehicles because the Image Processing Module A may reset unexpectedly, losing the rearview camera image and driver assistance features.
Becton Dickinson is recalling one lot of 10 mL Non-Sterile BD Luer-Lok Tip Syringes because some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
Medartis is recalling one lot of the APTUS 2.8 TriLock Screw 16 mm because of a mix up between specified lots of 2.5 mm and 2.8 mm outer diameter screws.
Altruan GmbH is recalling the Bisaf Strep A Self-Test, used to detect group A streptococcal antigens in throat swabs, because the product is not cleared by the FDA.
Altruan GmbH is recalling the Wondfo Streptococcal A At-Home Self-Test, used for group A beta-hemolytic streptococcal infection, because the product is not cleared by the FDA.
KOB GmbH is recalling Medline Unna-Z Stretch Zinc Paste Bandage because of a labeling error: the ingredients list did not include castor oil or calamine.
Uncle Ray's LLC is recalling Lowes Foods sour cream and onion flavored potato chips (8oz bags) due to inaccurate Nutrition Facts labels, including understated sodium content and undeclared monosodium glutamate.
Palmetto Gourmet Foods is recalling VEGETARIAN CHICKEN FLAVOR RAMEN Express (3oz packages) because it contains undeclared Yellow #5, an FDA-approved food colorant that must be labeled for consumers with sensitivities.
Medline is recalling three surgical kits containing Cardinal Health Aqua-Seal Chest Drainage Units because the instructions for use have been updated to clarify the target patient population as adults.
Medartis is recalling one lot of the APTUS 2.5 TriLock Screw 16 mm because of a mix up between specified lots of 2.5 mm and 2.8 mm outer diameter screws.
Altruan GmbH is recalling the Clearest Strep-A Cassette Test, used to detect group A streptococci in throat swab samples, because the product is not cleared by the FDA.
The outer cardboard box of C2O Coconut Water with Pulp (17.5 oz) 15-packs contains incorrect Nutrition Facts and Ingredient Lists that fail to disclose 5g of added sugar per can, although the can itself has correct labeling.
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