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 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.

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25701–25725 of 39704

  • SevereFDA (Food)·F-0237-2016·2015-11-25

    Kronos Foods Recalls Sample Assortment for Potential Metal Fragments

    Kronos Foods is recalling a 4-pound Sample Assortment of baked goods due to the potential for metal fragments. The recall covers 2 cases distributed to specific US states and one Canadian consignee.

    Product
    Sample Assortment Net WT 4 lbs. (1.82 kg) total weight of five trays bundled together. 38-68 pieces per tray Item number 11904 Manufactured by Kronos Foods Corporation, Madera, CA
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Drugs)·D-0372-2016·2015-11-25

    Downing Labs Recalls Piracetam Injection Due to Sterility Assurance Concerns

    Downing Labs, LLC is recalling Piracetam Injection, 200mg/mL, 10mL vials due to a lack of assurance of sterility. The recall covers all lots distributed nationwide and internationally.

    Product
    Piracetam Injection, 200mg/mL,10mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-332-2016·2015-11-25

    Essential Wellness Pharma Recalls TRIMIX #1 Injection Due to Sterility Concerns

    Essential Wellness Pharma is recalling TRIMIX #1 Injection vials because poor production practices may have compromised the sterility of the compounded sterile preparations.

    Product
    TRIMIX #1 Injection, 4.2 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0153-2016·2015-11-25

    Kar's Sweet n' Salty Mix Recalled for Possible Glass Contamination

    Kar Nut Products Company is recalling 208,008 bags of Kar's Sweet n' Salty Mix due to the possibility of very small pieces of glass in the product.

    Product
    Kar's Sweet n' Salty Mix 2 oz. flexible film bags. 72 bags per case.
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Devices)·Z-0285-2016·2015-11-25

    Prism Medical P-300 Portable Consumer Lift Recalled for Drive Shaft Failure

    ErgoSafe Products is recalling 1,721 Prism Medical P-300 Portable Consumer Lifts because the drive shaft and over speed arm may fail, potentially causing a patient to fall.

    Product
    Prism Medical P-300 Portable Consumer Lift; PN 303050, 303050R, and 303051; weight specification 300 lbs. /136 kg.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0292-2016·2015-11-25

    US Compounding Recalls Vitamin D3 Vials Due to Sterility Concerns

    US Compounding Inc is recalling 55 vials of Vitamin D3 in Olive Oil due to deficient practices that may impact sterility assurance.

    Product
    Vitamin D3 in Olive Oil (50,000 IU/mL) 30 mL vial, For IM Use only, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3277-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0296-2016·2015-11-25

    Fresenius Modified Mixer Motor Recalled Due to Fire Risk

    Fresenius Medical Care is recalling 992 Modified Mixer Motors for 132 Gallon Dissolution Units because they lack full thermal protection, posing a fire hazard.

    Product
    Fresenius Modified Mixer Motor (for 132 Gallon Dissolution Units), P/N 160075. For Use in the Preparation of acid concentrate for hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0256-2016·2015-11-25

    US Compounding Recalls Hyaluronic Acid Syringes Due to Sterility Concerns

    US Compounding Inc is recalling 531 hyaluronic acid and lidocaine syringes because deficient practices may have impacted sterility assurance.

    Product
    Hyaluronic Acid/Lidocaine PF (60 mg/2%), 3 mL Single Use Syringe, For Intra-Articular Injection , Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3249-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V796000·2015-11-24

    Mercedes-Benz Recalls 2015 S550E Hybrid Vehicles Due to Charger Defect

    Mercedes-Benz is recalling 2015 S550E Hybrid vehicles because a defective onboard charger may cause the car to unexpectedly shift to park, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S550E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V792000·2015-11-24

    Mercedes-Benz Recalls 2014 E350 Sedans for Fuel Line Fire Risk

    Mercedes-Benz is recalling 809 model year 2014 E350 sedans because a fuel feed line defect may cause a leak or disconnection, increasing the risk of fire or a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16045·2015-11-24

    SalesOne Recalls Light Up Ear Plug Jewelry Due to Burn Hazard

    SalesOne is recalling light-up ear plug jewelry sold at Spencer Gifts because battery acid can leak and cause burns. Consumers should stop wearing the product and contact SalesOne for a refund or replacement.

    Product
    Light up ear plug jewelry
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V791000·2015-11-24

    Wabash National Van Trailers Recalled for Brake Caliper Bolt Defect

    Wabash is recalling 2013-2015 Van Trailers because brake caliper bolts may not be tightened, risking caliper detachment and reduced braking.

    Product
    WABASH NATIONAL — WABASH NATIONAL VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V794000·2015-11-24

    Subaru Recalls 2016 Legacy and Outback for Drive Shaft Separation Risk

    Subaru is recalling 2016 Legacy and Outback vehicles because improperly tightened nuts may allow the drive shaft to separate, potentially causing a fuel leak and fire.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V790000·2015-11-24

    VT Hackney Recalls 2015 Kidron Refrigerated Trailers Due to Brake Defect

    VT Hackney is recalling certain 2015 Kidron Refrigerated Trailers because improperly tightened caliper bolts may allow the brake caliper to detach, reducing braking performance.

    Product
    KIDRON — KIDRON REFRIGERATED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V789000·2015-11-24

    Ford Recalls 2016 F-650 Trucks Due to Incorrect Steering Column

    Ford is recalling 2016 F-650 trucks built between July 29 and September 3, 2015, because an incorrect steering column may cause the park pawl to fracture, allowing the vehicle to move unexpectedly.

    Product
    FORD — FORD F-650 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V793000·2015-11-24

    Ford Recalls 2010-2011 Fusion and Mercury Milan for Fuel Leak Risk

    Ford is recalling 2010-2011 Fusion and Mercury Milan vehicles because fuel vapor canister purge valves may fail, causing fuel tank cracks and leaks that increase fire risk.

    Product
    MERCURY — MERCURY, FORD MILAN, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V781000·2015-11-23

    Strick Dry Freight Van Trailer Recall for Rear Impact Guard Defect

    Strick Trailers is recalling 1998-2005 Dry Freight Van Trailers because rear impact guards may fail to prevent vehicles from sliding underneath during a crash.

    Product
    STRICK — STRICK DRY FREIGHT VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V782000·2015-11-23

    BMW Recalls M3 and M4 Vehicles for Driveshaft Defect

    BMW is recalling 2015-2016 M3 and M4 vehicles because a driveshaft slip-joint may lack grease, potentially causing loss of power and increasing crash risk.

    Product
    BMW — BMW M3, M4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V776000·2015-11-20

    Navistar Recalls 2013-2014 International Trucks for Accelerator Pedal Defect

    Navistar is recalling 2013-2014 International trucks because a faulty accelerator pedal sensor can cause high engine idle, increasing crash risk on downgrades.

    Product
    INTERNATIONAL — INTERNATIONAL DURASTAR, WORKSTAR, TRANSTAR, LONESTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V774000·2015-11-19

    Utility Trailer Recalls 2015 VS2RA Models Due to Brake Caliper Bolt Issue

    Utility Trailer is recalling 2015 VS2RA Refrigerated Van trailers because improperly tightened caliper bolts may detach, reducing braking performance and increasing crash risk.

    Product
    UTILITY — UTILITY VS2RA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0229-2016·2015-11-18

    Miracle Rock 48 capsules recalled for containing undeclared thiosildenafil

    The One Minute Miracle Inc. is recalling Miracle Rock 48 capsules because they contain undeclared thiosildenafil, an unapproved drug analogue.

    Product
    MIRACLE ROCK 48 capsules, packaged in 2 x 2-count blisters, 4-count capsules per carton, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 0911312397354.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0182-2016·2015-11-18

    Appeeling Fruit Recalls Fresh Sliced Apples Due to Listeria Risk

    Appeeling Fruit Inc. is voluntarily recalling fresh sliced apples with specific dates due to potential Listeria monocytogenes contamination.

    Product
    Appeeling Fruit Inc.,Dauberville, PA 19533; Fresh Slices, Net Wt. 20 # Bulk, Best If Used By: 9/18/2015 Appeeling Fruit Inc., Dauberville, PA 19533 (bulk-packed), 4 CT/3 lb. Sweet Apple Slices Best If Used By: 9/18/2015. Packed 4 - 3lb boxes/case.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0189-2016·2015-11-18

    Andrew & Williamson Recalls Limited Edition Cucumbers Due to Salmonella Risk

    Andrew & Williamson Fresh Produce is recalling Limited Edition cucumbers because they may be contaminated with Salmonella. The recall affects 57,704 units distributed across 22 states.

    Product
    5/4 Limited Edition Cucumber Carton, Sizes 24SP, 36/36SP, 48. These cucumbers are shipped in a black, green, yellow, and craft colored carton which reads Limited Edition Pole Grown Cucumbers. This variety is often referred to as a Slicer or American cucumber. It has a dark…
    Category
    Food
    Distribution
    22 states
  • CriticalFDA (Food)·F-0190-2016·2015-11-18

    Andrew & Williamson Recalls Limited Edition Cucumbers Due to Salmonella Risk

    Andrew & Williamson Fresh Produce is recalling Limited Edition cucumbers because they may be contaminated with Salmonella.

    Product
    1 1/9 Bushel Limited Edition Cucumber Carton, Sizes: Plains (60-84 count), Extra Large (48 count), Large (60 count), Super Select (72 count), Super Select Special (84 count). These cucumbers are shipped in a black, green, yellow, and craft colored carton which reads Limited…
    Category
    Food
    Distribution
    22 states