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

14476–14500 of 31492

ModerateFDA (Devices)·Z-1336-2024·2024-03-27
FDA Recalls Vascular Guidewire Introducer Due to Manufacturing Defect
Angiodynamics is recalling 959 units of MINI STICK MAX guidewire introducers due to voids in the sheath hub that may prevent proper guidewire placement. Users may experience procedure delays and need to exchange equipment.
Product
MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-751
Category
Medical Device
Distribution
Distributed nationwide
CriticalCPSC·24169·2024-03-21
Happiness USA Roller Ball Candy Recalled Due to Choking Hazard
Twenty Four Six Foods LLC is recalling all flavors of Happiness USA Liquid Rolling Candy because the rolling ball applicator can dislodge into a child's mouth, posing a choking hazard and risk of death.
Product
Happiness USA Liquid Rolling Candy
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24171·2024-03-21
Starbucks-branded metallic mugs recalled due to burn and laceration hazards
Nestlé USA recalls about 440,500 metallic mugs from 2023 holiday Starbucks gift sets sold at Target, Walmart, and military retailers. The mugs can overheat or break when microwaved or filled with extremely hot liquid, causing severe burns and cuts. 10 people have been injured in 12 reported incidents.
Product
Metallic Mugs included in 2023 Holiday Starbucks-branded Gift Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24172·2024-03-21
BRS and BULin Liquid Fuel Bottles Recalled for Unsafe Closures
BRS and BULin portable liquid fuel bottles sold on Amazon have non-child-resistant closures that violate federal safety law, posing risks of burns and poisoning to children. Consumers should stop using them and contact the seller for disposal and refund instructions.
Product
BRS and BULin Liquid Fuel Bottles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24168·2024-03-21
Crown Aruba IV Gas Boilers Recalled for Carbon Monoxide Hazard
Crown Boiler Company is recalling about 1,100 Crown Aruba IV (AWR Series) gas-fired hot water boilers due to a blocked vent switch that can fail to shut down burners at high altitudes, allowing carbon monoxide to accumulate in homes.
Product
Crown Aruba IV (AWR Series) gas-fired hot water boilers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24174·2024-03-21
Ravin R500 Series Crossbows Recalled for Unexpected Discharge Injury Risk
Ravin Crossbows LLC is recalling about 13,300 R500 series crossbows because they can unexpectedly discharge while being cocked or uncocked if not fully cocked, posing an injury hazard. The company has received one report of unexpected discharge but no injuries have been reported.
Product
Ravin R500 Model Crossbows
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24167·2024-03-21
Fisher-Price Little People figures recalled due to detachable head choking hazard
Fisher-Price is recalling Mickey and Friends figures sold since May 2023 because Donald and Daisy Duck heads can detach, posing a choking hazard. Three detachments were reported, including one found in a child's mouth, with no injuries.
Product
Fisher-Price Little People Mickey and Friends Figures
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24166·2024-03-21
Culture Kings Sneaker Basel Magnetic Levitation Displays Recalled for Laceration and Ingestion Hazards
Culture Kings is recalling approximately 4,300 Sneaker Basel Magnetic Levitation Displays sold online from July 2020 through January 2023. The high-powered magnets can break and cause lacerations, or be swallowed and lodge in the digestive system, risking serious injury and death.
Product
Sneaker Basel Double Magnetic Levitation Displays
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Food)·F-1055-2024·2024-03-20
CK Turkey and Cheese Sandwich recalled for undeclared sesame allergen
CK Turkey and Cheese Sandwich is recalled for undeclared sesame allergen. The sandwich label lists only Wheat, Milk, and Soy allergens, missing sesame which poses risk to allergic consumers.
Product
CK Turkey and Cheese Sandwich, net wt. 6.7oz. Product is closed-face sandwich and ready to eat product. UPC 983644000141. The sandwich label declares "Ingredients: Multigrain Bread ***Contains: Wheat, Milk, Soy."
Category
Food
Distribution
0 states
SevereFDA (Food)·F-1071-2024·2024-03-20
Trader Joe's Southwest Salad Recalled Due to Listeria Monocytogenes Contamination
Trader Joe's Company is recalling Trader Joe's Southwest Salad (SKU 56077), 9 oz. due to potential Listeria monocytogenes contamination. Approximately 800,955 units were distributed nationwide.
Product
Trader Joe s Southwest Salad (SKU 56077) 9 oz.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1069-2024·2024-03-20
Trader Joe's Cilantro Salad Dressing Recalled for Listeria Contamination
Trader Joe's is recalling Cilantro Salad Dressing (SKU 36420) due to possible Listeria monocytogenes contamination. Approximately 15,890 cases were distributed nationwide.
Product
Trader Joe s Cilantro Salad Dressing (SKU 36420) Perishable Keep Refrigerated 12 FL OZ (355mL)
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1056-2024·2024-03-20
Food recall: Jacksons sandwich with undeclared sesame allergen
Capitol Commissary LLC recalled 1,382 units of Jacksons Turkey and Cheese Sandwich due to undeclared sesame. The product was distributed across seven Western states and may pose a risk to consumers with sesame allergies.
Product
Jacksons Turkey and Cheese Sandwich, net wt. 6.7oz. Product is closed-face sandwich and ready to eat product. UPC 983642601562. The sandwich label declares "Ingredients: Multigrain Bread ***Contains: Wheat, Milk, Soy."
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1284-2024·2024-03-20
Vascular guide catheter recalled due to distal end fracture risk
Medos is recalling CERENOVUS CEREBASE DA Guide Sheaths due to reports of fractures at the distal end. Fractures may delay surgical procedures or cause vascular injury.
Product
CERENOVUS CEREBASE DA Guide Sheath, Part Numbers: a) GS9080SD; b) GS9090SD; c) GS9095SD; Vascular guide-catheter, single-use
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-1070-2024·2024-03-20
Trader Joe's Elote Chopped Salad Kit Recalled for Listeria Contamination
Trader Joe's Company is recalling approximately 7,348 cases of Trader Joe's Elote Chopped Salad Kit nationwide due to potential Listeria monocytogenes contamination. All products with "Used By" dates on or before February 18, 2024 are affected.
Product
Trader Joe s Elote Chopped Salad Kit (SKU 74768) 11.94 oz.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1065-2024·2024-03-20
BrightFarms Southwest Chipotle Salad Kits Recalled for Listeria Contamination
BrightFarms Southwest Chipotle Salad Kits are being recalled for potential Listeria monocytogenes contamination in the cotija cheese ingredient. Affected products have best-by dates from December 31, 2023 through February 22, 2024.
Product
BrightFarms Southwest Chipotle Salad Kit Ready to eat salad kit containing green lettuce (grown by indoors at BrightFarms) and a master pack supplied by Latitude 36 Foods, which contain cotija cheese, dressing and toppings. Intended for retail distribution to consumers. Cotija
Category
Food
Distribution
0 states
HighFDA (Drugs)·D-0381-2024·2024-03-20
TRP Natural Eyes eye drops recalled due to lack of sterility assurance
TRP Natural Eyes Aging Eye Relief eye drops are being recalled because the manufacturer cannot assure the product meets sterility requirements. The recall affects 19,344 bottles distributed nationwide.
Product
TRP Natural Eyes Aging Eye Relief, Sterile Eye Drops, Homeopathic, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-027-15.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0373-2024·2024-03-20
Pfizer Bicillin L-A Prefilled Syringes Recalled for Improper Storage
Mckesson is recalling Bicillin L-A prefilled syringes stored outside label specifications. The FDA Class II recall affects 70 vials distributed to direct accounts in NM, AZ, and UT.
Product
Bicillin L-A (Penicillin G Benzathine) 1.2, MMU / 2 mL Injection Prefilled Syringe 2 mL, Rx only, Mfg: Pfizer Pharmaceuticals, NDC 60793-0701-10
Category
Drug
Distribution
3 states
HighFDA (Drugs)·D-0375-2024·2024-03-20
TRP Natural Eyes Allergy Relief Eye Drops Recalled for Sterility Assurance Issues
Optikem International is recalling TRP Natural Eyes Allergy Eyes Relief eye drops due to lack of assurance of sterility. The recall affects 30,240 bottles distributed nationwide.
Product
TRP Natural Eyes Allergy Eyes Relief, Sterile Eye Drops, Homeopathic 0.33 FL OZ (10mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-032-15.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1292-2024·2024-03-20
Shimadzu Trinias Digital Angiography System Recalled for Capacitor Defect
Shimadzu has recalled the Trinias Digital Angiography System due to a capacitor manufacturing issue that could cause abnormal display or system malfunction. No injuries have been reported.
Product
Shimadzu, Trinias, Digital Angiography System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0372-2024·2024-03-20
Infuvite Adult Multiple Vitamins Injection Recalled for Storage Deviation
Baxter Healthcare's Infuvite Adult Multiple Vitamins Injection is being recalled because 70 vials were stored outside their labeled specifications, potentially affecting product stability. The affected vials were distributed to three direct accounts in Arizona, New Mexico, and Utah.
Product
Infuvite Adult Multiple vitamins injection, single-dose vial 5mL, Rx only, MFG: Baxter Healthcare Corp., NDC 54643-5649-01
Category
Drug
Distribution
3 states
HighFDA (Food)·F-1068-2024·2024-03-20
The Perfect Bite Co. frozen corn bites recalled due to listeria risk
The Perfect Bite Co. is recalling Mexican Street Corn Bites due to possible Listeria monocytogenes contamination. The product was distributed in California and Washington.
Product
The Perfect Bite Co. Mexican Street Corn Bites 36 count Net Wt 29.9 oz (1lb 13.9oz) 847g UPC: 813341015752. Frozen product, packaged in a paper carton.
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1278-2024·2024-03-20
D-Clip Applier Recalled for Failure to Release During Surgery
Peter Lazic GmbH's D-Clip Standard/Mini Applier is being recalled after a customer complaint that the device failed to release the clip during surgery, with the applier remaining attached to the clip.
Product
D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1290-2024·2024-03-20
CARTO VIZIGO Guiding Sheath Recalled for Manufacturing Validation Issue
Biosense Webster is recalling CARTO VIZIGO Bi-Directional Guiding Sheaths after inadvertently mixing unvalidated devices into production. The recall affects 853 units distributed nationwide.
Product
CARTO VIZIGO Bi-Directional Guiding Sheath, REF D128502 The CARTO VIZIGOTM Bi-Directional Guiding Sheath is designed to provide accessibility and maneuverability in the cardiac anatomy. The steerable sheath is fitted with a hemostasis valve to minimize blood loss during cathe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0379-2024·2024-03-20
TRP Eye Strain Relief Eye Drops Recalled Due to Lack of Sterility Assurance
Optikem International recalls TRP Eye Strain Relief eye drops nationwide due to lack of assurance of sterility. Affected units are 10 mL bottles with Lot E206.
Product
TRP Eye strain Relief, Sterile Eye Drops, Homeopathic, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-172-15.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0370-2024·2024-03-20
Potassium Chloride Injection Recalled Due to Pinhole Container Defects
B. Braun Medical is recalling 22,752 bags of Potassium Chloride for Injection Concentrate nationwide due to pinholes in container bags that compromise sterility assurance. Affected lots are J2S007 (expires 12/31/2024) and J3A115 (expires 01/31/2025).
Product
POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide

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14476–14500 of 31492