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.

Filters

Agency

Category

Minimum severity

Clear filters

21151–21175 of 39673

  • SevereNHTSA·17V187000·2017-03-17

    Entegra Motorhomes Recalled for Front Suspension Ball Joint Separation Risk

    Entegra is recalling specific Aspire, Cornerstone, and Anthem motorhomes because front suspension ball joints may loosen and separate, potentially causing a loss of steering control.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE, ANTHEM, ASPIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·023-2017 EXP·2017-03-17

    King's Command Foods Recalls Beef Products Due To Foreign Matter

    King's Command Foods is recalling approximately 63,252 pounds of ground beef products, including meatballs and beef fritters, due to possible contamination with extraneous materials such as metal.

    Product
    King's Command Foods, LLC — King's Command Foods, LLC. Recalls Beef Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·026-2017·2017-03-16

    Flagship Food Group Recalls Frozen Burritos Due to Plastic Contamination

    Flagship Food Group is recalling approximately 8,622 pounds of frozen breakfast burritos sold at Trader Joe's in Illinois and Pennsylvania due to possible hard clear plastic contamination.

    Product
    Flagship Food Group — Flagship Food Group Recalls Frozen Burrito Product Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Devices)·Z-1257-2017·2017-03-15

    Physio-Control Recalls LIFEPAK 1000 Defibrillators for Unexpected Power-Offs

    Physio-Control is recalling 133,330 LIFEPAK 1000 defibrillators worldwide because they may unexpectedly power off during use.

    Product
    The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR and the use of the LIFEPAK 1000 defibrillator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1567-2017·2017-03-15

    Grove Fresh Apple Juice Recalled for Undeclared Milk Allergen

    Dairy Maid Dairy is recalling Grove Fresh Pasteurized Apple Juice from concentrate due to undeclared milk, a major allergen.

    Product
    Grove Fresh Pasteurized Apple Juice from concentrate, 4-ounce cartons, 100 % Pure.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1409-2017·2017-03-15

    FDA Recalls Premier Guard Drape Due to Sterility Compromise

    The FDA is recalling Premier Guard Drape, Sterile, because the sterile barrier was breached, compromising sterility. The product is used with RF Surgical Gauze detection systems.

    Product
    Premier Guard Drape, Sterile. For Use with Verisphere (01-0035) and ArQ.Sphere (01-0044) Item Number: 01-0037 Used in conjunction RF Surgical Gauze detection systems to protect scanning device from contamination during various surgical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1428-2017·2017-03-15

    Villa Sistemi Medicali Recalls Apollo X-Ray Systems Due to Footrest Detachment

    Villa Sistemi Medicali is recalling 65 Apollo multi-function x-ray systems because the footrest detached from the table, causing a patient to fall.

    Product
    Apollo; Models: 9784000131 9784000231 9784020131 9784020231 9784100231 9784120131 9784120231 9784130131 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1408-2017·2017-03-15

    FDA Recalls Premier Guard Sterile Drapes Due to Sterility Compromise

    The FDA is recalling Premier Guard Sterile Drapes because the sterile barrier was breached, compromising sterility. The recall covers 1,111,600 units distributed nationwide.

    Product
    Premier Guard Sterile Drape For Use with Blair-Port Wand (02-0029) and Blair-Port Wand X (01-0046) Item Number: 01-0020 Used in conjunction RF Surgical Gauze detection systems to protect scanning device from contamination during various surgical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0513-2017·2017-03-15

    McKesson Recalls Aspirin Chewable Tablets Due to Foreign Material

    McKesson Packaging Services is recalling 6,717 cartons of 81 mg Aspirin Chewable Tablets because foreign material was found in the bulk inventory.

    Product
    Aspirin Chewable Tablets, 81 mg, (NSAID*), packaged in UD 750 Tablets (25 x 30) tablets in blisters per carton, Dist. By: McKesson Packaging Services, a business unit of McKesson Corporation, 7101 Weddington Rd., Concord, NC 28027, NDC 63739-434-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1432-2017·2017-03-15

    Siemens PRIMUS HI and Mevatron M2 Linear Accelerators Recalled for Weld Defect

    Siemens is recalling 35 PRIMUS HI and Mevatron M2 linear accelerators due to a defective weld seam that could cause overhead suspensions to fall and injure people.

    Product
    PRIMUS HI and Mevatron M2/Primus Mid-Energy, Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0492-2017·2017-03-15

    Mylan Recalls Mirtazapine Tablets Due to Foreign Glipizide Contamination

    Mylan Pharmaceuticals is recalling Mirtazapine tablets because bottles may contain foreign Glipizide 10 mg tablets. Consumers should stop using the product and contact their pharmacist.

    Product
    MIRTAZAPINE — MIRTAZAPINE (MIRTAZAPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1433-2017·2017-03-15

    Siemens Medical Recalls 35 MEVATRON M 6700 Linear Accelerators

    Siemens Medical Solutions USA is recalling 35 MEVATRON M 6700 linear accelerators due to a defective weld seam that could cause the overhead suspension to fall and injure a patient or other person.

    Product
    MEVATRON M 6700 (MX) Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1430-2017·2017-03-15

    Villa Sistemi Medicali Recalls Apollo EZ X-Ray Systems Due to Footrest Detachment

    Villa Sistemi Medicali is recalling 65 Apollo EZ x-ray systems because the footrest detached from the table, causing a patient to fall.

    Product
    Apollo EZ; Model: 9784152036 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1532-2017·2017-03-15

    Pharmanex ageLOC TR90 Protein Boost Recalled for Undeclared Milk Allergen

    Nu Skin is voluntarily recalling Pharmanex ageLOC TR90 Protein Boost because it contains an undeclared milk allergen.

    Product
    Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt. 1.59 lbs (720g). 30 Servings. Natural Vanilla Flavor. Lactose, Gluten, & Soy Free. Plant Protein/Vegetarian.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1429-2017·2017-03-15

    Apollo DRF X-ray Systems Recalled Due to Footrest Detachment Hazard

    Villa Sistemi Medicali is recalling 65 Apollo DRF x-ray systems because the footrest can detach, causing patients to fall from the table.

    Product
    Apollo DRF; Model: 9784220831 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1437-2017·2017-03-15

    Siemens MEVATRON KD-2 Linear Accelerators Recalled for Defective Weld Seams

    Siemens is recalling 35 MEVATRON KD-2 linear accelerators due to defective weld seams that could break and cause the overhead suspension to fall, posing a risk of severe injury.

    Product
    MEVATRON KD-2, accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1436-2017·2017-03-15

    Siemens Medical Linear Accelerators Recalled for Defective Overhead Suspension Welds

    Siemens is recalling 35 linear accelerator systems due to defective weld seams that could cause overhead suspensions to fall, posing a risk of severe injury.

    Product
    MEVATRON MD-2, MEVATRON MDX-2 and MEVATRON ME, accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·025-2017·2017-03-15

    RBR Meat Company Recalls Frozen Supreme Pizza Due to Listeria Risk

    RBR Meat Company is recalling approximately 21,220 pounds of frozen Marketside Extra Large Supreme Pizza due to possible Listeria monocytogenes contamination.

    Product
    RBR Meat Co., Inc. — RBR Meat Company, Inc. Recalls Frozen Pizza Product Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1585-2017·2017-03-15

    Versa Marketing Recalls Fusia Szechuan Stir Fry Due to Listeria

    Versa Marketing is recalling Fusia Asian Aspirations Szechuan Stir Fry because the product tested positive for Listeria monocytogenes. The recall affects 4,089 cases sold at Aldi stores nationwide.

    Product
    Fusia Asian Aspirations Szechuan Stir Fry; A delicious blend of premium vegetables with a savory sauce packed in a plastic bag: Sauce packet included. NET WT 21 oz. (1 lb 5 oz) 595 g
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1434-2017·2017-03-15

    Siemens Medical Linear Accelerators Recalled for Defective Weld Seams

    Siemens is recalling 35 MEVATRON M 6730/6740 linear accelerators because defective weld seams on overhead suspensions could break and fall, posing a risk of severe injury.

    Product
    MEVATRON M 6730/6740 (MEX) Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide