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

9526–9550 of 31231

HighFDA (Food)·F-0341-2025·2025-01-08
Tropical Fruit Cup Products Recalled for Possible Listeria Contamination
King Kullen and Gracie's Kitchen brand tropical fruit cups may contain Listeria monocytogenes. Affected products were distributed in Connecticut and New York with sell-by dates from 11/11 to 11/21/24.
Product
a.) King Kullen brand Tropical Fruit Cup; UPC: 85316-10384; 16 oz plastic container b.) King Kullen brand Tropical Fruit Cup; UPC: 85316-10403; 12 oz plastic container c.) Gracie's Kitchen brand Tropical Fruit Cup; UPC: 85316-10384; 16 oz plastic container d.) Gracie's Kitchen br
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0793-2025·2025-01-08
Medline custom surgical procedure kits recalled for non-sterile components
Medline is recalling 182 custom surgical procedure kits containing non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. The kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) CERVICAL PACK-LF, REF DYNJ0867145G; 2) CERVICAL SPINE PACK HUM-LF, REF DYNJ35184F; 3) ANTERIOR CERVICAL-CORPECTOMY, REF DYNJ904827.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0780-2025·2025-01-08
Medline custom surgical procedure kits recalled for non-sterile components and endotoxin contamination
Medline custom procedure kits containing non-sterile Codman Surgical Patties & Strips are being recalled due to potential endotoxin contamination. The recall affects 74 units distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER SUPPLEMENT, REF DYNJ69476; 2) DIEP FLAP, REF DYNJ910120
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0781-2025·2025-01-08
Medline Nasal Pack Procedure Kits Recalled for Potential Endotoxin Contamination
Medline custom nasal pack procedure kits contain non-sterile surgical components with potential endotoxin contamination. Customers should discontinue use and contact Medline.
Product
Medline custom medical procedure kits labeled as: 1) NASAL PACK, REF DYNJ67789A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0174-2025·2025-01-08
Injectable phenylephrine recalled due to defective tamper-evident seals nationwide
Hikma Injectables is recalling phenylephrine injections nationwide because tamper-evident seals on some syringes were not properly attached. Affected lot 243120003D has a use-by date of 03/11/2025.
Product
phenylephrine in 0.9% Sodium Chloride Inj, 1mg per 10 mL (100 mcg/mL), Rx only, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, NDC 63037-173-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0787-2025·2025-01-08
Medline Surgical Procedure Kits Recalled Due to Sterility Concerns
Medline is recalling custom surgical procedure kits that contain non-sterile surgical supplies with potential for endotoxin contamination. The kits were distributed worldwide, including the United States, United Arab Emirates, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF, REF DYNJ39461J; 2) NEURO BASIN KIT, REF DYNJ80200B.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0332-2025·2025-01-08
Fajita Mix Products Recalled for Potential Listeria Contamination
Gracie's Kitchens Inc. is recalling King Kullen and Gracie's Kitchen brand Fajita Mix products distributed in Connecticut and New York due to potential Listeria monocytogenes contamination.
Product
a.) King Kullen brand Fajita Mix; UPC: 85316-11090; 12 oz plastic container b.) Gracie's Kitchen brand Fajita Mix; UPC: 85316-10002; 12 oz plastic container
Category
Food
Distribution
2 states
HighFDA (Food)·F-0346-2025·2025-01-08
Fruit Platters Recalled Due to Potential Listeria Contamination
Fruit Platters sold under King Kullen and Gracie's Kitchen brands may contain Listeria monocytogenes. Consumers in Connecticut and New York who purchased products with November 11-21, 2024 sell-by dates should not eat them.
Product
a.) King Kullen brand Large Fruit Platter; UPC: 85316-10402; 56 oz plastic container b.) Gracie's Kitchen brand Large Fruit Platter; UPC: 85316-10402; 56 oz plastic container
Category
Food
Distribution
2 states
HighFDA (Drugs)·D-0167-2025·2025-01-08
Levothyroxine Sodium tablets recalled for impurity specification failure
Lupin Pharmaceuticals is recalling Levothyroxine Sodium 75 mcg tablets due to out-of-specification impurities detected in stability testing. Affected lot LA01276 (expiring 07/2026) was distributed to one Ohio distributor.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
0 states
HighFDA (Devices)·Z-0789-2025·2025-01-08
Medline MICRODISECTOMY PACK recalled for endotoxin contamination
Medline custom MICRODISECTOMY PACK kits containing non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination are being recalled. Approximately 1,494 units were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) MICRODISECTOMY PACK, REF DYNJ80585A; 2) MICRODISECTOMY PACK, REF DYNJ80585B.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0794-2025·2025-01-08
Medline surgical procedure kits recalled for non-sterile components and endotoxin contamination
Medline is recalling 474,300 custom surgical procedure kits because they contain non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. These components could pose infection risks during surgical procedures.
Product
Medline custom medical procedure kits labeled as: 1) CRANI, REF CDS780089V; 2) CRANIOFACIAL CDS, REF CDS780102K; 3) CRANIOFACIAL CDS, REF CDS780102L; 4) CRANIOFACIAL CDS, REF CDS780102M; 5) CRANIOTOMY CDS-LF, REF CDS780105K; 6) CRANIOTOMY CDS-LF, REF CDS780105L; 7) CRANIO
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V597000·2025-01-08
2023 Ford Explorer turbocharger oil supply line may leak
Ford is recalling certain 2023 Explorer vehicles with 2.3L GTDI engines because the turbocharger oil supply line may be damaged, causing oil leaks that increase the risk of engine fire or stall.
Product
FORD — 2023 FORD EXPLORER
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25087·2025-01-08
SIG SAUER ROMEO5 Red Dot Firearm Sights Recalled Due to Button Battery Ingestion Hazard
SIG SAUER recalled about 230,000 ROMEO5 red dot sights because the included button cell battery can be easily accessed and lacks required child-resistant packaging, posing a serious ingestion hazard to children.
Product
SIG SAUER ROMEO5 Red Dot Sights
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0326-2025·2025-01-08
Honeydew Slices and Chunks Recalled for Listeria Contamination Risk
Honeydew slices and chunks sold under King Kullen, Wild By Nature, and Gracie's Kitchen brands may be contaminated with Listeria monocytogenes. Affected products were distributed in Connecticut and New York with sell-by dates from November 9-21, 2024.
Product
a.) King Kullen brand Honeydew Slices; UPC 85316-10009; 20 oz foam tray b) Wild By Nature brand Honeydew Slices; UPC: 85316-10009; 20 oz foam tray c.) King Kullen brand Honeydew Chunks; UPC: 85316-10382; 16 oz plastic container d.) King Kullen brand Honeydew Chunks; UPC: 85316-10
Category
Food
Distribution
2 states
HighFDA (Food)·F-0333-2025·2025-01-08
Brussel Sprout Products Recalled for Potential Listeria Contamination
Gracie's Kitchens Inc. is recalling brussel sprout products sold under King Kullen, Wild by Nature, and Gracie's Kitchen brands due to potential Listeria monocytogenes contamination. Affected products were distributed in Connecticut and New York.
Product
a.) King Kullen brand Brussel Sprout Halves; UPC: 85316-10097; 12 oz plastic container b.) King Kullen brand Brussel Sprouts Shredded; UPC: 85316-10098; 12 oz plastic container c.) Wild by Nature brand Brussel Sprout Halves; UPC: 85316-10097; 12 oz plastic container d.) Gracie's
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0773-2025·2025-01-08
Medtronic Implantable Drug Pumps Recalled for Software Defects
Medtronic has recalled 566 SynchroMed II and III implantable drug infusion pumps due to software issues in the controlling application. No injuries or illnesses have been reported.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2.x, CFN CT900D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0792-2025·2025-01-08
Medline Medical Procedure Kits Recalled for Non-Sterile Component Contamination
Medline Industries is recalling 2,664 custom medical procedure kits containing non-sterile surgical components with potential endotoxin contamination. The affected kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF, REF DYNJ47568B; 2) UROLOGY ROBOTIC, REF DYNJ55555D; 3) KIT,SPINE LH, REF DYNJ906448A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0173-2025·2025-01-08
Ketamine injection syringes recalled due to missing tamper-evident seals
Hikma Injectables is recalling 1,800 ketamine injection syringes nationwide because tamper-evident seals are not attached to several syringes, compromising sterility assurance.
Product
ketamine inj 50 mg per 1 mL, Rx Only, 1 mL fill in a 3mL pre-filled syringe, For IV or IM Use, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, This is a Compounded Drug. Hospital/Office Use Only. NDC 63037-137-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0772-2025·2025-01-08
SynchroMed II and III implantable pumps recalled for software issues
Medtronic recalled SynchroMed II and III implantable pumps for software issues in the clinician tablet application. Fifty-nine systems are affected.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with the A810 CP app version 2.x, CFN CT900C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0354-2025·2025-01-08
Gracie's Kitchen Diced Carrots recalled for potential Listeria monocytogenes contamination
Gracie's Kitchen brand Diced Carrots may be contaminated with Listeria monocytogenes. The recall affects 3,681 cases distributed in Connecticut and New York with sell-by dates between November 12-22, 2024.
Product
a.) Gracie's Kitchen brand Diced Carrots; UPC: 85316-10019; 10 oz plastic container
Category
Food
Distribution
2 states
ModerateFDA (Drugs)·D-0175-2025·2025-01-08
Carboxymethylcellulose sodium eye drops recalled for label mix-up
AvKARE is recalling Carboxymethylcellulose Sodium Ophthalmic Solution eye drops due to a label mix-up. The recall affects 16,677 cartons distributed nationwide.
Product
CARBOXYMETHYLCELLULOSE SODIUM — CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0168-2025·2025-01-08
AvKARE Nitrofurantoin 100 mg Capsules Recalled for Dissolution Failures
AvKARE is recalling Nitrofurantoin 100 mg capsules (NDC 50268-625-15, lot 47101, exp. 02/2026) nationwide because they failed dissolution specifications. Affected users should consult their healthcare provider.
Product
Nitrofurantoin Capsules, USP, 100 mg, 50 Capsules (5 x 10) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478. NDC#: 50268-625-15.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0375-2025·2025-01-08
Wegmans Jalapeno Baked Cheese Puffs Recalled for Undeclared MSG
Herr Foods Inc is recalling Wegmans Jalapeno Baked Cheese Puffs due to undeclared monosodium glutamate and flavor compounds. Affected units have expiration dates from December 2024 through May 2025.
Product
Wegmans Jalapeno Baked Cheese Puffs, Jalapeno flavored, 10oz, (283 g), SKU #6877
Category
Food
Distribution
1 state
ModerateFDA (Drugs)·D-0176-2025·2025-01-08
Eye drops recalled nationwide due to labeling mix-up
AvKARE is recalling Polyvinyl Alcohol Ophthalmic Solution eye drops due to a labeling mix-up. The recall affects Lot #0160 and was distributed nationwide.
Product
POLYVINYL ALCOHOL — POLYVINYL ALCOHOL (POLYVINYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0171-2025·2025-01-08
Dapsone Gel Recalled Nationwide for Crystallization
Viona Pharmaceuticals is recalling Dapsone Gel 7.5% nationwide due to crystallization detected in multiple lots. Patients should contact their pharmacy or healthcare provider for guidance.
Product
DAPSONE — DAPSONE (DAPSONE)
Category
Drug
Distribution
Distributed nationwide

How to read this listing

Filters

9526–9550 of 31231