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

14226–14250 of 27736

HighFDA (Food)·F-0798-2024·2024-02-07
Benny T's hot sauce recalled for undisclosed wheat allergen
Benny T's Vesta Dry Hot Sauce is recalled because the label does not disclose wheat, a major allergen present in the breadcrumb ingredient. People with wheat allergies or celiac disease should not consume this product.
Product
the original BENNY T'S VESTA DRY HOT SAUCE HOT NET WT. 1.5OZ INGREDIENTS: Fresh Chilies, Onions, Breadcrumbs (enriched flour, water, sugar, yeast, salt, non-hydrogenated vegetable shortening), Olive Oil, Salt, Natural Preservatives. UPC 7 94571 99497 3 (Jalapeno & Habanero)
Category
Food
Distribution
24 states
HighFDA (Devices)·Z-0817-2024·2024-02-07
Custom Cardiac Procedural Kits Recalled for Inadequate Sterilization Assessment
American Contract Systems is recalling 4394 custom cardiac procedural kits due to components added without proper assessment for sterilization exposure, which may result in loss of functionality or drug efficacy.
Product
Custom procedural convenience kits and trays, cardiac, labeled as: a) HEART CATHETERIZATION TRAY, kit number JRHC45G; b) TAVR PACK, kit number LLTV10; c) CATH PED LF SJH, kit number SJCA21F; d) CATH HEART ADL LF SJH, kit number SJCH22F; e) INT RAD PORTS-LF - 206060, ki
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0902-2024·2024-02-07
Knee Replacement Component Recalled for Potential Material Oxidation and Degradation
Howmedica Osteonics is recalling TRIDENT 0 deg knee implant components manufactured with aged raw material that may have elevated oxidation levels, potentially affecting material properties.
Product
HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-32J
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0917-2024·2024-02-07
Knee Replacement Tibial Inserts Recalled Due to Material Oxidation Risk
Knee replacement tibial inserts from Howmedica may have elevated oxidation if manufactured with raw material over 5 years old, potentially affecting material properties.
Product
DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product Number: 6642-1-911
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0911-2024·2024-02-07
Knee replacement implant recalled due to material oxidation risk
Howmedica is recalling knee replacement implants manufactured with UHMWPE material over 5 years old due to potential oxidation that could affect material properties.
Product
RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement Product Number: 6637-0-831
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0800-2024·2024-02-07
Hot Sauce Recalled for Missing Wheat Allergen Labeling
Benny T's Vesta Dry Hot Sauce is recalled for labeling that fails to disclose wheat and other ingredient common names. The missing allergen information poses a risk to consumers with wheat allergies.
Product
the original BENNY T'S VESTA DRY HOT SAUCE SCORPION NWT WT. 1.5OZ INGREDIENTS: Fresh Chilies, Onions, Breadcrumbs (enriched flour, water, sugar, yeast, salt, non-hydrogenated vegetable shortening), Olive Oil, Salt, Natural Preservatives. UPC 7 94571 99491 1 (Trinidad Moruga Sc
Category
Food
Distribution
24 states
HighFDA (Drugs)·D-0280-2024·2024-02-07
IV Phenylephrine Bags Recalled Due to Potential Double-Dose Delivery System Malfunction
Denver Solutions is recalling 12,564 bags of PHENYLephrine HCl IV solution nationwide due to a semi-automated filling system malfunction that could dispense double doses to patients.
Product
PHENYLephrine HCl 40 mg per 250 mL 0.9% Sodium Chloride (160 mcg per mL), Item F3352, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-150-82.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0872-2024·2024-02-07
Knee replacement implant recalled for material oxidation risk
Howmedica Osteonics is recalling SCORPIO RECESSED PATELLA knee replacement components due to potential oxidation of the UHMWPE material in units manufactured with raw material over 5 years of age.
Product
SCORPIO RECESSED PATELLA-Intended for knee repalcment Part Number: 3044-0032
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V487000·2024-02-07
Mazda recalls 2014-2018 Mazda3 and CX-3 for faulty rearview cameras
Mazda is recalling 2014-2018 Mazda3 and 2016-2021 CX-3 vehicles because rearview cameras may display flickering or distorted images, reducing visibility and increasing crash risk. Dealers will inspect and replace cameras free of charge.
Product
MAZDA — 2014 MAZDA MAZDA3
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0806-2024·2024-02-07
Aldi Choceur Burnt Caramel Chocolate Bars Recalled for Undeclared Coconut
Astor Chocolate Corp. has recalled Aldi Choceur Burnt Caramel Chocolate Bars due to undeclared coconut, a common allergen. The voluntary recall involves 1,092 units distributed to a distribution center in Florida.
Product
Aldi Choceur Burnt Caramel Chocolate Bars, Net Wt. 1.75oz. UPC 4099100202809
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0885-2024·2024-02-07
Knee Replacement Insert Recalled Due to Potential Material Oxidation
Howmedica Osteonics is recalling Scorpio-Flex knee prosthesis inserts due to potential oxidation in UHMWPE raw material over 5 years old, which could impact material properties.
Product
Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for knee replacement Part Number: 72-16-0910
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0899-2024·2024-02-07
Knee Replacement Component Recalled Due to Material Oxidation Risk
Howmedica Osteonics is recalling Scorpio NRG Tibial Brg Insert Assembly knee replacement components due to potential oxidation of raw materials over 5 years of age, which could affect material properties.
Product
Scorpio NRG Tibial Brg Insert Assy -Intended for knee replacement Part Number: 82-2-0908
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0921-2024·2024-02-07
Knee replacement implant recalled due to potential material degradation
Howmedica Osteonics recalls DUR PCA MTK REV INS RT knee replacement implants due to potential oxidation of UHMWPE material that could compromise material properties. Patients should contact their healthcare provider.
Product
DUR PCA MTK REV INS RT Intended for knee replacement Product Number: 6728-2-709
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0276-2024·2024-02-07
Budesonide Extended-Release Tablets recalled for failed dissolution specifications
Golden State Medical Supply Inc. is recalling 108 bottles of Budesonide Extended-Release Tablets (9 mg) distributed in Illinois due to failed dissolution specifications.
Product
Budesonide Extended-Release Tablets, 9 mg, 30-count bottles, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA, UPC 5140782430, NDC 51407-824-30
Category
Drug
Distribution
0 states
HighFDA (Devices)·Z-0954-2024·2024-02-07
MRI Machine Coil Seal Adhesive May Create Sharp Edges
The Intera Achieva 1.5T Pulsar MRI machine's Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients. All units of this model are affected.
Product
Intera Achieva 1.5T Pulsar. Model (REF) Number 781171.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0963-2024·2024-02-07
Medline Adult Blood Culture Kits Recalled Due to Unlabeled Component Expiration Dates
Medline is recalling specific Adult Blood Culture Kits because the expiration date of an internal Bactec component is not reflected on the kit insert, creating a risk of using an expired component.
Product
MEDLINE ADULT BLOOD CULTURE KIT, Reorder Number DYNDH1694A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0890-2024·2024-02-07
Knee replacement implant recalled due to material oxidation risk
Howmedica Osteonics is recalling a knee replacement patellar component that may have been manufactured with oxidized raw material. Products using UHMWPE over 5 years old can develop elevated oxidation and degraded material properties.
Product
SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #11 -Intended for knee replacement Part Number: 73-2110
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0825-2024·2024-02-07
Surgical Procedure Kits Recalled Due to Improper Sterilization
American Contract Systems is recalling 7,881 surgical procedure kits nationwide because components were sterilized without proper validation, risking loss of functionality or elevated chemical residue.
Product
Custom procedural convenience kits and trays, general & plastic surgery, labeled as: a) BRACHY THERAPY PROCEDURE PAC, kit number AGBR90E; b) BRACHY THERAPY PROCEDURE PAC, kit number AGBR90E; c) MINI MINOR AGH ASC PACK, kit number AGMM60M; d) OUTPATIENT PORT ACCESS KIT 3
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0812-2024·2024-02-07
ToYou Snacks Mango Yogurt Bars Recalled for Undeclared Soy Allergen
Font Group of America Corp. is recalling ToYou Snacks brand Mango Yogurt bars due to undeclared soy allergen. Affected units were distributed in the United States.
Product
Mango Yogurt bar, ToYou Snacks Brand, 1.41 Oz/ 40 g, packaged in kraft laminated paper, 14 bars in 1 box.
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-0832-2024·2024-02-07
Ophthalmic procedural kits recalled due to inadequate sterilization validation
American Contract Systems is recalling 940 ophthalmic surgical kits nationwide due to undocumented components that may lack functionality, drug efficacy, or contain elevated sterilization residuals.
Product
Custom procedural convenience kits and trays, Ophthalmic use, labeled as: a) EYE PACK, kit number LVEY27; b) Laminectomy, kit number UIOL34AG
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0811-2024·2024-02-07
Mint Dark Chocolate bars recalled for undeclared soy allergen
Font Group of America is recalling Mint Dark Chocolate bars (ToYou Snacks Brand) due to undeclared soy allergen. Consumers with soy allergies should not consume the product.
Product
Mint Dark Chocolate bar, ToYou Snacks Brand, 1.41 Oz/ 40 g, packaged in kraft laminated paper, 14 bars in 1 box.
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-0932-2024·2024-02-07
Volar Bearing Plate wrist fixation systems recalled for bearing dislodgement
TriMed Inc. recalls Volar Bearing Plate wrist fixation systems because bearings may dislodge from distal peg holes during implantation, potentially compromising fracture fixation. Approximately 270 units distributed in five states.
Product
Volar Bearing Plate. REF: VBEAL-3-7N, VBEAL-5-7N, VBEAL-3-7S, VBEAL-5-7S, VBEAL-7-7S, VBEAL-3-7W, VBEAL-5-7W, VBEAR-3-7N, VBEAR-5-7-N, VBEAR-3-7S, VBEAR-5-7S, VBEAR-7-7S, VBEAR-3-7W, VBEAR-5-7W. Intended to be used as an aid to the treatment of certain types of fractures,
Category
Medical Device
Distribution
5 states
HighFDA (Devices)·Z-0834-2024·2024-02-07
Endoscopic Surgical Stapler Reload May Fail to Form Complete Staple Line
An endoscopic surgical stapler reload may fail to properly form staples during use, potentially leaving tissue inadequately sealed. This could lead to bleeding or require additional surgery.
Product
ENDOPATH ECHELON 45mm RELOADS WITH GRIPPING SURFACE TECHNOLOGY (GST), ECHELON Endopath Stapler, Endoscopic Linear Cutter Reload (+Gripping Surface technology), 45MM WHITE VASCULAR/THIN, Product No. GST45W
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V488000·2024-02-07
Tesla Model S and Model X seat belts may detach in crash
Tesla is recalling certain 2021-2023 Model S and Model X vehicles because front-row seat belts may not be connected properly to pretensioner anchors and could detach. A detached seat belt may fail to properly restrain an occupant during a crash.
Product
TESLA — 2023 TESLA MODEL S
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0869-2024·2024-02-07
Knee replacement patella component recalled due to material oxidation risk
Howmedica Osteonics Corp. is recalling SCORPIO RECESSED PATELLA knee replacement components manufactured from UHMWPE raw material over 5 years of age, which may develop elevated oxidation affecting material properties.
Product
SCORPIO RECESSED PATELLA- Intended for Knee Replacement Part Number: 3044-0026
Category
Medical Device
Distribution
Distributed nationwide

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14226–14250 of 27736