The Recall Desk

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.

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8051–8075 of 36567

  • SevereFDA (Devices)·Z-0717-2022·2022-03-16

    Luscient Diagnostics COVID-19 Antigen Test Kits Recalled for Lack of FDA Authorization

    Lusys Laboratories' Luscient Diagnostics COVID-19 Antigen Test Kits are being recalled because they lack FDA authorization. The kits were not approved, cleared, or authorized for distribution in the United States.

    Product
    Luscient Diagnostics 2nd Generation of COVID-19 Viral Antigen Test For all mutant variety Cat: I-114(Nasal Swab Test)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0957-2022·2022-03-16

    Abbott Infant Formula Powder Recalled for Bacterial Contamination

    Abbott Laboratories is recalling infant formula powder due to potential contamination with Cronobacter sakazakii and Salmonella Newport. Consumer complaints related to these pathogens in infants have been reported.

    Product
    Abbott Infant Formula Powder 12.6oz. can. 6 cans per case. Item numbers: Clinical Retail UPCs: N/A - Clinical
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0919-2022·2022-03-16

    Abbott Similac Human Milk Fortifier Recalled Due to Pathogen Risk

    Abbott Similac Human Milk Fortifier pouches are recalled due to potential Cronobacter sakazakii and Salmonella Newport contamination. The recall affects infants who may have received contaminated product.

    Product
    Abbott Similac Human Milk Fortifier 0.9g Pouch / Sachet, 50 Pouch / Sachet per retail unit. 3 retail units per case Item numbers: 54598 5459813 5459814 5459820 5459886 6771009 Retail UPCs: 70074545998 070074545998 055325545996 070074109404 070074103297 07007467
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0827-2022·2022-03-16

    Taiwan Best Quality Enoki Mushrooms Recalled for Listeria Contamination

    Jan Fruits, Inc. is recalling Taiwan Best Quality Enoki Natural Mushrooms due to Listeria monocytogenes contamination found by California Department of Public Health. Approximately 617 cases were distributed in California.

    Product
    Taiwan Best Quality Enoki Natural Mushrooms, Premium 200g/7.5 oz. clear plastic package. 50 pcs per box. Manufacturer: Changhua County Mushroom Production Cooperative; Distributed by Jan Fruits. UPC: 8 51084 00835 8
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0949-2022·2022-03-16

    Abbott EleCare Infant Formula Recalled for Potential Cronobacter and Salmonella

    Abbott Laboratories is recalling EleCare infant formula nationwide and worldwide due to potential contamination with Cronobacter sakazakii and Salmonella Newport. Consumer complaints related to these pathogens have been received involving infants.

    Product
    Abbott EleCare Amino Acid-Based Powder Infant Formula with Iron 14.1oz. can, Abbott Elecare 400g. can, Abbott Elecare Unflavored 14.1oz. can. 6 cans per case. Item numbers: 55251 5525157 5525189 Retail UPCs: 070074535111 070074116297 070074119854
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0953-2022·2022-03-16

    Abbott EleCare Jr Nutrition Powder Recalled Due to Bacterial Contamination

    Abbott is recalling EleCare Jr Amino Acid-Based Nutrition Powder due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants. The bacteria was also found in the manufacturing facility.

    Product
    Abbott EleCare Jr Amino Acid-Based Nutrition Powder Chocolate 14.1oz. can. 6 cans per case. Item numbers: 66273 Retail UPCs: 070074662718
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0716-2022·2022-03-16

    LuSys COVID-19 Antigen Test Kits Recalled for Lack of FDA Authorization

    Lusys Laboratories is recalling 14,745 kits of COVID-19 antigen test kits that lack FDA clearance, approval, or emergency use authorization. The kits were distributed nationwide and internationally without required regulatory validation.

    Product
    LuSys 2nd Generation of COVID-19 Viral Antigen Test For all mutant variety Cat: I-114(Saliva Test)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0943-2022·2022-03-16

    Abbott Similac 360 Infant Formula recalled for Cronobacter and Salmonella

    Abbott is recalling Similac 360 Total Care Infant Formula due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants, with Cronobacter found in the manufacturing facility.

    Product
    Abbott Similac 360 Total Care Infant Formula with Iron 20.6oz. and 30.3oz. palstic jar. 4 jars per case. 7oz. can. 6 cans per case. Item numbers: 68063 68065 68109 Retail UPCs: 070074680644 070074680668 070074681108
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0652-2022·2022-03-16

    Oxycodone Hydrochloride Oral Solution Recall Due to Impurity Failure

    American Health Packaging is recalling one lot of Oxycodone Hydrochloride Oral Solution due to impurity failure detected at initial testing of the repackaged product.

    Product
    OXYCODONE HYDROCHLORIDE — OXYCODONE HYDROCHLORIDE (OXYCODONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0946-2022·2022-03-16

    Abbott Similac Organic Infant Formula recalled for Cronobacter and Salmonella

    Abbott Similac Organic with A2 Milk Infant Formula is being recalled following consumer complaints related to Cronobacter sakazakii and Salmonella Newport in infants, plus evidence of Cronobacter in the manufacturing facility.

    Product
    Abbott Similac Organic with A2 Milk Infant Formula with Iron 8oz. and 7oz. can. 6 cans per case. 20.6oz. plastic jar. 4 jars per case. Item numbers: 67904 68016 68099 Retail UPCs: 070074677545 070074680170 070074681009
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0927-2022·2022-03-16

    Abbott Similac Alimentum Infant Formula Recalled for Bacterial Contamination

    Abbott Laboratories recalls Similac Alimentum Infant Formula with Iron due to potential Cronobacter sakazakii and Salmonella Newport contamination. Consumer complaints related to infections in infants and manufacturing facility contamination prompted the FDA Class I recall.

    Product
    Abbott Similac Alimentum Infant Formula with Iron 12oz. can. 6 jars per case; 19.8oz. can. 4 cans per case; 7oz. can. 6 cans per case Item numbers: 64715 64717 64719 Retail UPCs: 070074647128 070074647166 070074647180
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0952-2022·2022-03-16

    Abbott EleCare Jr Amino Acid Powder Recalled for Pathogenic Bacteria

    Abbott EleCare Jr Amino Acid-Based Nutrition Powder (banana) is recalled due to consumer complaints of Cronobacter sakazakii or Salmonella Newport in infants, with pathogen evidence in the manufacturing facility.

    Product
    Abbott EleCare Jr Amino Acid-Based Nutrition Powder Banana 14.1oz. can. 6 cans per case. Item numbers: 66275 Retail UPCs: 070074662763
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V161000·2022-03-16

    KZRV Recalls 2022 Travel Trailers Due to Improperly Welded Couplers

    KZRV is recalling 2022 Stratus, Connect, Sonic, and SportTrek travel trailers because improperly welded couplers may cause the trailer to separate from the tow vehicle.

    Product
    KZRV — KZRV SONIC, STRATUS, SPORT TREK, CONNECT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V157000·2022-03-15

    2022 Winnebago travel trailers recalled for improperly welded couplers

    Winnebago is recalling certain 2022 Micro Minnie, Minnie, and Voyage travel trailers because the coupler was improperly welded, which may cause the trailer to separate from the tow vehicle and increase crash risk.

    Product
    WINNEBAGO — WINNEBAGO MICRO MINNIE, MINNIE, VOYAGE!
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V158000·2022-03-15

    Kia Recalls 2014-2016 Cadenza for Windshield Bonding Defect

    Kia is recalling 2014-2016 Cadenza vehicles because the front windshield may not be properly bonded, posing a risk of detachment.

    Product
    KIA — KIA CADENZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V159000·2022-03-15

    Great Dane Recalls 2022 Trailers Due to Loose Suspension Bolts

    Great Dane is recalling 2022 Champion and Everest trailers because suspension bolts were not properly tightened, posing a crash risk.

    Product
    GREAT DANE — GREAT DANE CHAMPION, EVEREST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V154000·2022-03-14

    2021–2022 Dodge Durango and Jeep Grand Cherokee Steering Recall

    Chrysler is recalling 2021–2022 Dodge Durango and 2022 Jeep Grand Cherokee vehicles due to steering gear defect. The rack bar may have been insufficiently hardened, potentially causing loss of steering control.

    Product
    JEEP — JEEP, DODGE GRAND CHEROKEE 4XE, DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E018000·2022-03-11

    Norco Frames Recalled for Improperly Welded Couplers

    Norco Industries is recalling certain frames with Model CA-5400 couplers due to improper welding that may cause trailer separation.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V153000·2022-03-11

    Thomas Built Buses Recalls Saf-T-Liner EFX School Buses for Seat Bolt Defect

    Daimler Trucks North America is recalling 2020-2023 Thomas Built Buses Saf-T-Liner EFX school buses because passenger seat mounting bolts may break, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V150000·2022-03-11

    Ford Recalls F-150, Expedition, Navigator for Brake Master Cylinder Leak

    Ford is recalling 2016-2018 F-150, 2016-2017 Expedition, and Navigator vehicles because a brake master cylinder leak may reduce front brake function and increase crash risk.

    Product
    FORD — FORD, LINCOLN F-150, EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V143000·2022-03-11

    Forest River 2022 Travel Trailers Recalled for Coupler Weld Defect

    Forest River is recalling certain 2022 travel trailers due to improperly welded couplers that may cause trailer separation from the tow vehicle. Dealers will replace the coupler at no charge.

    Product
    FOREST RIVER — FOREST RIVER, EAST TO WEST XLR TOYHAULER, SILVER LAKE, VIBE, DELLA TERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0815-2022·2022-03-09

    Vadilal Quick Treat Custard Apple Pulp Recalled for Salmonella

    Vadilal Industries is recalling Quick Treat Custard Apple Pulp (1kg packages, UPC 8901777282168) due to potential Salmonella contamination. Approximately 997 cases were distributed nationwide to retail stores.

    Product
    Vadilal Quick Treat Custard Apple Pulp Net Wt, 1kg/35.27-oz. Product code FPEP44302 UPC:8901777282168 Best Before September 2023
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0806-2022·2022-03-09

    Whole Foods Market Vanilla Shortbread Cookies Recalled Due to Undeclared Egg

    Whole Foods Market Vanilla Shortbread Cookies are recalled due to undeclared egg allergen. The 23 units distributed in Washington D.C. with pack date 1/20/22 may pose serious risk to consumers with egg allergies.

    Product
    Whole Foods Market Vanilla Short Bread Cookies packaged in clear plastic container with a white scale label applied PLU 66705
    Category
    Food
    Distribution
    1 state