Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

24951–24975 of 26084

HighFDA (Devices)·Z-2238-2021·2021-08-18
Prelude SNAP cardiac introducer sheath potentially mislabeled with wrong size
Merit Medical Systems is recalling Prelude SNAP Splittable Sheath Introducers (10F size) because 7F sheaths may have been packaged with 10F labels. This error affects 760 units in lot I2067768.
Product
Prelude SNAP Splittable Sheath Introducer, REF: PLSX -1010, size 10F, Standard Length: 13 cm, CE0344, STERILE EO, Rx Only, (01) 00884450489611. For the introduction of various types of pacing leads and catheters to the heart and coronary venous system.
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-2249-2021·2021-08-18
Bard Bone Marrow Aspiration Needles Recalled for Incomplete Packaging Seals
Bard Peripheral Vascular is recalling Illinois Bone Marrow Aspiration/Intraosseous Infusion Needles due to incomplete or open packaging seals that could compromise sterility. Approximately 1,200 devices are affected.
Product
TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x 79mm TIN3015 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 15G x 79mm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2229-2021·2021-08-18
Shent USA Grasper/Retriever Endoscopic Instruments Recalled for Mislabeling
Shent USA is recalling Grasper/Retriever endoscopic instruments (lot 020377208) due to mislabeling. Products bearing one catalog number may contain different devices with different jaw specifications, potentially resulting in wrong instrument selection.
Product
Grasper/Retriever, Alligator Jaw 2.4 mm x 5 mm x 230 cm Catalog Number: 7208 Intended use: single use accessory devices used through the working channel of a GI endoscope
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2271-2021·2021-08-18
Biomet Hip Replacement Component Recalled Over Corrosion and Device Failure Risk
Biomet is recalling Arcos Modular Revision Hip System components that may develop fretting corrosion in the inner taper, risking device failure and the need for revision surgery. Affected patients should contact their healthcare provider.
Product
Arcos Modular Revision Hip System High Offset Cone Prox Body, Size C, 70 MM Item Number: 11-301333
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0853-2021·2021-08-18
5000 Years Foods Kimchi Recalled for Listeria Contamination Risk
5000 Years Foods is recalling NO MSG Sliced Cabbage Kimchi sold in multiple container sizes due to potential Listeria monocytogenes contamination. The product was distributed in Illinois and may have reached customers nationwide through retail stores.
Product
5000 Years Foods NO MSG SLICED CABBAGE KIMCHI in 5GAL plastic tubs, and 128 oz, 64 oz, 32 oz, & 16 oz glass jars
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2219-2021·2021-08-18
Michael Graves Stryker Highback Chair distributed to home users instead of healthcare facilities
Stryker Medical Division recalled its Michael Graves Highback Chair (Model 4853) after it was distributed to residential customers instead of healthcare facilities. Home users may not understand safety instructions written for trained medical professionals.
Product
Michael Graves with Stryker Highback Chair-intended for pediatric and adult person guest and patient seating use in an indoor medical setting, Model Number 4853, Part #4853000000 ¿
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2253-2021·2021-08-18
Medical imaging software displays anatomical orientation tags incorrectly
Simpleware ScanIP medical imaging software contains a bug where anatomical orientation tags display incorrectly. This could lead to operator misunderstanding and errors during image resampling and realignment.
Product
Simpleware ScanIP software. For transfer of imaging information from a medical scanner to an output file, and for simulating/evaluating surgical treatment options.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0847-2021·2021-08-18
BUBS Naturals MCT Oil Powder Recalled for Undeclared Milk Allergen
Slayer Forever, LLC (dba BUBS Naturals) is recalling BUBS Naturals MCT Oil Powder dietary supplement because the product contains undeclared milk allergens.
Product
BUBS Naturals MCT OIL Powder, Medium Chain Triglycerides from 100% virgin Coconut Oil. Dietary Supplement 10.6 oz. Gusset Bags
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2232-2021·2021-08-18
Medline Knee Arthroscopy Kit Recalled for Expired Irrigation Component
Medline Industries is recalling 286 knee arthroscopy kits containing an expired NaCl irrigation bag. The kits should not be used due to the expired component.
Product
Medline Knee Arthroscopy Kit, convenience kit, REF DYNJ902838C, containing expired component NaCl 3000mL Irrigation Bag (exp. date 08/01/2020).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2206-2021·2021-08-18
Stryker Surgistool Model 830 distributed to home users instead of healthcare professionals
Stryker Medical recalls a surgical support tool that was distributed to home consumers but is intended only for healthcare professionals. The device labeling is correct, but home users may lack training to use it safely.
Product
Surgistool-intended to support a healthcare professional during surgical procedures Model 830, Part Number 0830000000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2277-2021·2021-08-18
Spectrum Medical Quantum Standard Heat Exchanger Sterilization Defect Recall
QURA S.R.L. is recalling 1088 units of Spectrum Medical Quantum Standard heat exchangers that may not be adequately sterilized. The devices also lack required 510(k) clearance for US distribution.
Product
Spectrum Medical Quantum Standard heat exchanger
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2263-2021·2021-08-18
Biomet Hip Implant Cone Bodies Recalled Due to Fretting Corrosion Risk
Biomet is recalling 22 units of Arcos hip implant cone bodies that may develop inner taper fretting corrosion, potentially causing device failure and requiring surgical intervention.
Product
Arcos Modular Revision Hip System High Offset Cone Prox Body, Size A, 60 MM Item Number: 11-301311
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21181·2021-08-18
Hallmark Teether Rings Recalled Due to Choking Hazard
Hallmark is recalling approximately 15,500 wooden teether rings with plush attachments because the wooden ring can break into small parts, creating a choking hazard. The company has received four reports of the rings breaking, including one case where a child placed broken pieces in their mouth.
Product
Teether Rings with Decorative Fabric and Plush Attachments
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2276-2021·2021-08-18
Automated diagnostic analyzer from Abbott recalled for waste pressure buildup
Abbott is recalling 260 Alinity s System analyzers due to a design defect allowing waste pressure to build up and spray operators. No injuries reported.
Product
Alinity s System REF 06P16-01. An automated immunoassay analyzer for In Vitro diagnostic use in blood donor screening, plasma and plasmapheresis screening, and organ donor centers, hospitals, and reference laboratories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2214-2021·2021-08-18
S3 MedSurg hospital beds recalled from residential sale due to misuse risk
Stryker's S3 MedSurg hospital beds designed for healthcare facilities were distributed to home customers. The device labeling is correct but home users may not understand professional-use instructions, posing a risk of improper operation.
Product
S3 MedSurg Bed - intended to support and transport patients within the Med/Surg and Critical Care hospital environments, Model Number 3002, Part 3002S3CUSTOM, 3002S3EX, 3002S3PATRIOT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2252-2021·2021-08-18
Dutch Ophthalmic Vitrectomy Pack Contains Mismatched Infusion Line Gauge
Dutch Ophthalmic USA is recalling TDC Vitrectomy Pack VGPC 25g surgical kits. The packages are labeled as containing 25-gauge infusion lines but actually contain 23-gauge lines instead.
Product
The device is a 25-gauge infusion line that is part of 25-gauge surgical pack labeled TDC Vitrectomy Pack VGPC 25g, Product Number 8525.201.
Category
Medical Device
Distribution
Distributed nationwide
CriticalCPSC·21179·2021-08-17
Zen Magnets and Neoballs Magnets Recalled Due to Ingestion Hazard
Zen Magnets and Neoballs high-powered spherical magnets are being recalled because swallowing multiple magnets can cause intestinal perforation, blockage, and death. About 10 million magnets sold individually and in sets since January 2009 are affected.
Product
Zen Magnets and Neoballs Magnets
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V642000·2021-08-17
Newmar motorhomes recalled for fuel hose leak fire risk
Newmar is recalling 2021-2022 motorhomes with Cummins L9 diesel engines due to a potential fuel leak from a fuel hose that could cause fire.
Product
NEWMAR — 2022 NEWMAR NEW AIRE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V636000·2021-08-13
2021 Grand Design Imagine trailers recalled for incorrect axle bearings
Grand Design is recalling certain 2021 Imagine recreational trailers with Dexter D30 axles due to incorrect inner bearings. The bearings can cause wheels to lock or reduce stopping ability, increasing crash risk.
Product
GRAND DESIGN — 2021 GRAND DESIGN IMAGINE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21773·2021-08-12
Rossignol All Track DH Bicycles Recalled Due to Fall Hazard
Rossignol is recalling 2018 and 2019 model year All Track DH bicycles because cracks can form at the head tube weld, causing the fork and front wheel to separate from the frame during use and create a fall hazard.
Product
Rossignol 2018 and 2019 Model Year All Track DH Bicycles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·21774·2021-08-12
YOH Super Soft Purple Rugs Recalled Due to Fire Hazard
About 100 YOH Super Soft Purple Rugs sold on Amazon.com fail to meet federal flammability standards, posing a fire hazard. Consumers should stop using them immediately.
Product
YOH Super Soft Purple Rugs
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Food)·F-0825-2021·2021-08-11
Great Value Chocolate Chip Snack Muffins Recalled for Listeria Contamination
Give and Go Prepared Foods is recalling Great Value Chocolate Chip Snack Muffins nationwide because they may be contaminated with Listeria monocytogenes, a harmful bacterium that can cause serious foodborne illness.
Product
Great Value Chocolate Chip Snack Muffin - 12 oz, 8 per case; UPC 078742-33100 3
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0816-2021·2021-08-11
Grimmway Farms Carrot Chunks Recalled for Potential Salmonella
Grimmway Enterprises, Inc. is recalling peeled carrot chunks sold in bulk because they may be contaminated with Salmonella. Consumers should not consume the affected product and should contact their retailer or the company for more information.
Product
Carrots Chunk Peeled 2" Grimmway Farms Sold in bulk - 50 lb., 25 lbs.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0810-2021·2021-08-11
Organic Baby Carrots Recalled Due to Salmonella Contamination Risk
Grimmway Farms is recalling Bunny Luv brand organic cut and peeled baby carrots nationwide due to potential Salmonella contamination. Affected products are 1 lb. bags with lot codes beginning with 195, 196, or 197 and ending in BF or SP.
Product
Organic Cut and Peeled Baby Carrots Brand name: Bunny Luv 1 lb.(454 g) plastic bag UPC: 0 3338390205 0;
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0749-2021·2021-08-11
Vy&Tea herbal tea recalled for unapproved drug ingredient sibutramine
Qikmoov LLC is recalling Vy&Tea herbal tea because FDA analysis detected sibutramine, an ingredient not approved in an NDA or ANDA application. The product was marketed and distributed nationwide and internationally.
Product
Vy&Tea (Vietnamese Labeling with a green leaf and a bird underneath) 15/KLT 45.0G (15 tea sachets per box), Manufactured by Havyco No. 45, Group 1, National Highway 14, Son Hiep Hamlet, Tho Son Commune, Bu Dang District, Binh Phuoc Province, Vietnam, Website: trathaomocgiamcan.co
Category
Drug
Distribution
Distributed nationwide

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