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 the agency’s own highest classification or reported deaths or serious injuries, 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

12301–12325 of 89681

HighFDA (Devices)·Z-2144-2024·2024-06-26
VICRYL Sutures recalled due to packaging defect compromising sterility
Ethicon recalls 341,532 units of VICRYL surgical sutures worldwide due to holes in primary packaging that compromise sterility and could result in infection.
Product
VICRYL (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic surgery, but not for use in cardiovascular and neurological tissues. PRODUCT CODE: J214H J218H J258H J268H J269H J327H…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1387-2024·2024-06-26
Caramel Confectionery Drops Recalled for Potential Salmonella Contamination
Clasen Quality Chocolate Inc. is recalling 4M Caramel Flavored Confectionery Drop due to potential Salmonella contamination. The product was distributed to nine states.
Product
4M Caramel Flavored Confectionery Drop, Item # 61661 (R&D Sample).
Category
Food
Distribution
9 states
HighFDA (Drugs)·D-0559-2024·2024-06-26
Cefixime Oral Suspension Recalled for Failed Content Uniformity Specifications
Lupin Pharmaceuticals is recalling one lot of Cefixime oral suspension (200 mg/5 mL) due to failed content uniformity specifications. The recall affects 3,552 bottles distributed nationwide.
Product
CEFIXIME — CEFIXIME (CEFIXIME)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2161-2024·2024-06-26
Xstar Safety Slit Knife Recalled for Incorrect Blade Bevel Orientation
Beaver Visitec International is recalling the Xstar Safety Slit Knife Model 378227 because some units have the blade bevel installed incorrectly—facing downward instead of the intended upward orientation.
Product
Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2157-2024·2024-06-26
OPTETRAK Inset Patella knee implants recalled for improper vacuum packaging
Exactech is recalling OPTETRAK Inset Patella knee implants packaged in out-of-specification vacuum bags that may compromise product integrity during storage or sterilization.
Product
OPTETRAK Inset Patella, Item Numbers: a) 200-05-23, 23MM; b) 200-05-26, 26MM; c) 200-05-29, 29MM
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2153-2024·2024-06-26
Howmedica Gray Revision Instrument Tray Recalled for Design Enabling Instrument Reuse
Howmedica is recalling the Gray Revision Instrument System Accessory Tray/Case due to a design flaw that may enable reuse and re-sterilization of single-use, sterile-packaged instruments.
Product
Gray Revision Instrument System Accessory Tray/Case, Catalog/Part Number: 6210-9-910
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2146-2024·2024-06-26
PDS II Polydioxanone Sutures Recalled Due to Compromised Sterility
Ethicon is recalling 56,952 units of PDS II polydioxanone sutures distributed worldwide because a packaging defect resulted in compromised sterility, which could lead to infection. No illnesses have been reported.
Product
PDS II (polydioxanone) Suture - Intended for use in general soft tissue approximation, including use in paediatric cardiovascular tissue, in microsurgery and in ophthalmic surgery. These sutures are particularly useful where the combination of an absorbable suture and extended…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1385-2024·2024-06-26
Milk Chocolate Confectionery Coating Recalled for Potential Salmonella
Clasen Quality Chocolate Inc. is recalling Milk Chocolate Flavored Confectionery Coating Bulk (Item #60692) due to potential Salmonella contamination. The product was distributed across nine U.S. states.
Product
Milk Chocolate Flavored Confectionery Coating Bulk (MB), Item # 60692.
Category
Food
Distribution
9 states
HighFDA (Food)·F-1377-2024·2024-06-26
Heinen's Tuscan Salad Bowl recalled for undeclared pecan allergen
Heinen's Tuscan Salad Bowl is recalled due to the presence of undeclared pecans, a known allergen not listed on the label. Consumers with pecan allergies face a risk of allergic reaction.
Product
Heinen's Tuscan Salad Bowl Ingredients: Garbanzo Beans***Disodium EDTA***Arugula, Roasted Corn***Red Bell Pepper, Dried Cranberries***Walnuts***Parmesan Cheese*** Contains: WALNUT, MILK
Category
Food
Distribution
2 states
HighFDA (Drugs)·D-0560-2024·2024-06-26
White Petrolatum Jelly Mislabeled With Undisclosed Lavender and Chamomile
Consumer Product Partners is recalling Pure Petroleum white petrolatum products sold at Rite Aid, Kroger, Harris Teeter, and CVS nationwide because the products labeled as pure white petrolatum actually contain undisclosed lavender and chamomile.
Product
PURE PETROLEUM — PURE PETROLEUM (WHITE PETROLATUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2151-2024·2024-06-26
Hospital bed mattress covers may delaminate from improper cleaning
Baxter Healthcare is recalling Centrella Max and Pro+ hospital bed mattresses that may develop delaminated top covers when cleaned with bleach-containing solutions. The mattresses prevent and treat pressure injuries.
Product
Centrella Max - The Centrella Smart+ Bed is intended for use in healthcare environments as a patient support system to prevent and/or treat pressure injuries.Multiple model numbers of Centrella Max mattresses and pro+ mattresses. (1) Centrella Max Surface, REF P7922A01; (2)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1380-2024·2024-06-26
Milk Chocolate Flavored Confectionery Coating Recalled for Potential Salmonella
Clasen Quality Chocolate Inc. is recalling Milk Chocolate Flavored Confectionery Coating (Item #58710) due to potential Salmonella contamination. The bulk tanker product was distributed across nine states.
Product
Milk Chocolate Flavored Confectionery Coating (MB), Item #: 58710. Bulk tanker.
Category
Food
Distribution
9 states
HighFDA (Food)·F-1381-2024·2024-06-26
White Chocolate Wafer Recalled for Potential Salmonella Contamination
Clasen Quality Chocolate Inc. is recalling 74,050 pounds of White Chocolate Wafer due to potential Salmonella contamination. The product was distributed to food service and ingredient suppliers across nine states.
Product
White Chocolate Wafer, Item # 59152. Net Wt. 50 lbs (22.68kg). Clasen Quality Chocolate 5126 West Terrace Drive, Madison, WI 53718
Category
Food
Distribution
9 states
HighFDA (Devices)·Z-2155-2024·2024-06-26
Exactech Knee Patella Components Recalled Due to Out-of-Specification Vacuum Bags
Exactech is recalling OPTETRAK Three Peg Patella knee components packaged in out-of-specification vacuum bags. The affected products were distributed worldwide.
Product
OPTETRAK Three Peg Patella, Item Numbers: a) 200-02-26, 26MM; b) 200-02-29, 29MM; c) 200-02-32, 32MM; d) 200-02-35, 35MM; e) 200-02-38, 38MM; f) 200-02-41, 41MM;
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-1383-2024·2024-06-26
Milk Chocolate Coating Recalled for Potential Salmonella Contamination
Clasen Quality Chocolate Inc. is recalling Milk Chocolate Flavored IC Coating distributed in nine states due to potential Salmonella contamination. The product is sold in bulk tanker format for use in food manufacturing.
Product
1057556 Milk Chocolate Flavored IC Coating, Item # 56546. Bulk tanker.
Category
Food
Distribution
9 states
HighFDA (Food)·F-1384-2024·2024-06-26
Clasen Quality Chocolate Recalls Milk Chocolate Crunch Bulk for Salmonella
Clasen Quality Chocolate Inc. is recalling Milk Chocolate Crunch Bulk OTBD for potential Salmonella contamination. The product was distributed across nine U.S. states.
Product
Milk Chocolate Crunch Bulk OTBD, Item # 56546.
Category
Food
Distribution
9 states
HighNHTSA·24V477000·2024-06-26
Polestar 2 infotainment software may prevent the rearview camera displaying
Polestar is recalling certain 2021-2024 Polestar 2 vehicles because Infotainment Head Unit software may prevent the rearview camera image from displaying, failing FMVSS 111.
Product
POLESTAR — POLESTAR POLESTAR 2
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2152-2024·2024-06-26
Storage Case Design Flaw May Allow Reuse of Single-Use Surgical Instruments
Howmedica Osteonics Corp. is recalling HRIS Storage & Sterilization Cases (Part 6210-9-900) due to a design flaw that may allow reuse and resterilization of single-use, sterile instruments. This poses a contamination and infection risk.
Product
HRIS Storage & Sterilization Case and Tray, Catalog/Part Number: 6210-9-900
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2160-2024·2024-06-26
NxStage PureFlow-B Hemodialysis Solution Bags Recalled Due to Bursting Chambers and Caustic Fluid
NxStage PureFlow-B hemodialysis solution bags may burst during preparation, releasing caustic electrolyte fluid that can cause chemical burns. Affected units are distributed nationwide.
Product
NxStage PureFlow-B Solution, Premixed Dialysate for Hemodialysis, Device Catalog Numbers RFP-400, RFP-401, RFP-402, RFP-403, RFP-404, RFP-405, RFP-406, RFP-453, RFP-454, RFP-456
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2145-2024·2024-06-26
FDA Recalls VICRYL Plus Antibacterial Sutures Due to Packaging Defect
Ethicon is recalling VICRYL Plus Antibacterial Sutures due to a packaging machine defect that created holes in the primary packaging, potentially compromising product sterility. Affected sutures may pose an infection risk.
Product
VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, except for ophthalmic, cardiovascular and neurological tissues. PRODUCT CODE: VCP196H VCP417H VCP602H VCP603H VCP662H VCPB259H…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2148-2024·2024-06-26
MONOCRYL Surgical Sutures Recalled for Packaging Sterility Defect
Ethicon recalls 306,000 MONOCRYL surgical sutures worldwide due to holes in primary packaging from a manufacturing defect that compromises sterility and could result in infection.
Product
MONOCRYL (poliglecaprone 25) Suture - Intended for use in general soft tissue approximation and/or ligation where an absorbable material is indicated PRODUCT CODE: Y315H Y345H Y359H Y398H Y416H Y417H Y426H Y427H Y935H Y936H Y945H
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2147-2024·2024-06-26
PDS Plus Antibacterial Surgical Sutures Recalled for Compromised Sterility
Ethicon recalls PDS Plus Antibacterial sutures due to packaging defects that compromised sterility. The affected units may cause infection if used in surgery.
Product
PDS Plus Antibacterial (polydioxanone) Suture - Intended for use in general soft tissue approximation, including use in paediatric cardiovascular tissue, in microsurgery and in ophthalmic surgery. These sutures are particularly useful where the combination of an absorbable…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0555-2024·2024-06-26
FDA Recalls Dexamethasone Sodium Phosphate Injection Due to Impurity Specification Failure
Eugia US LLC recalls 70,125 vials of Dexamethasone Sodium Phosphate injection due to failed impurity specifications. Testing found sulfonic acid adduct of dexamethasone phosphate exceeded allowed limits.
Product
DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2162-2024·2024-06-26
Xstar Safety Slit Knife Recalled for Incorrect Blade Configuration
Beaver Visitec International is recalling 126 Xstar Safety Slit Knives with incorrect blade configuration. The recalled knives have the bevel oriented to the back instead of the front.
Product
Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227, a component of CustomEye Kits, Numbers 584562, 5800109
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0557-2024·2024-06-26
Little Remedies Gas Relief Drops Class II Recall for Manufacturing Deviations
Denison Pharmaceuticals recalls 113,544 bottles of Little Remedies Gas Relief Drops (Lot #0855, exp. 8/31/2025) due to manufacturing deviations. All units have been recovered and controlled at the manufacturer.
Product
LITTLE REMEDIES — LITTLE REMEDIES (SIMTHICONE)
Category
Drug
Distribution
0 states

How to read this listing

Filters

12301–12325 of 89681