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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36026–36050 of 39777

  • SevereFDA (Devices)·Z-0147-2013·2012-10-31

    DePuy Mitek Recalls SPIRALOK Bone Fixation Anchors Due to Fracture

    DePuy Mitek is recalling 66 SPIRALOK bone fixation anchors because they can fracture after surgery, requiring patients to undergo revision surgery.

    Product
    Screw, fixation, boneProduct Number: 222967 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-024-2013·2012-10-31

    Raritan Recalls Leader Fiber Capsules Due to C. Difficile Contamination

    Raritan Pharmaceuticals is recalling Leader Fiber Capsules due to possible C. difficile contamination found in raw materials.

    Product
    Leader Fiber Capsules, 100% Natural Psyllium Fiber Laxative, Dietary Fiber Supplement, Relieves Constipation, Restores Regularity, 100 capsules per bottle, Distributed by: Cardinal Health, Dublin, OH 43017 www.myleader.com, NDC 37205-372-78, UPC 0-96295-11222-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0143-2013·2012-10-31

    SpiraLok 6.5mm Anchors Recalled Due to Post-Operative Fracture

    DePuy Mitek is recalling 372 units of SpiraLok 6.5mm anchors because they fractured after surgery, requiring patient revision.

    Product
    SpiraLok 6.5mm with Panacryl and needles Product Number: 222963 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0149-2013·2012-10-31

    DePuy Mitek Recalls SpiraLok 5.0 Anchors Due to Post-Operative Fracture

    DePuy Mitek is recalling SpiraLok 5.0 anchors because they may fracture after surgery, requiring revision. The recall covers all lot codes distributed worldwide.

    Product
    SpiraLok 5.0 w/out Needles with Orthocord Product Number: 222969 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0111-2013·2012-10-31

    Ethicon Recalls EVICEL Fibrin Sealant Pressure Regulators Due to Embolism Reports

    Ethicon is recalling EVICEL Fibrin Sealant pressure regulators after reports of air or gas embolism associated with the use of spray devices.

    Product
    EVICEL Fibrin Sealant (Human) Rx Only. Manufacturer: Omrix Biopharmaceuticals Ltd. MDA blood bank, Sheba Hospital, Ramat-Gan, POB 888, Kiryat Ono 55000 Israel U.S. License No. 1603. Distributed by: Ethicon, Inc. P.O. Box 151, Somerville, NJ 08876-0151 USA. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0145-2013·2012-10-31

    SpiraLok 5.0mm Anchors Recalled for Post-Operative Fracture Risk

    DePuy Mitek is recalling 232 units of SpiraLok 5.0mm anchors due to post-operative fractures requiring patient revision surgery.

    Product
    SpiraLok 5.0mm with Panacryl without needles Product Number: 222965 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0310-2013·2012-10-31

    Jer's Chocolates Recalls Peanut Butter Bars Due to Salmonella Risk

    Jer's Chocolates is voluntarily recalling specific peanut butter products because the peanut butter supplier, Sunland, Inc., recalled its products for potential Salmonella contamination.

    Product
    Peanut Butter Bars Toffee: 1) 3.0 oz, Two-Bar Box, Toffee, UPC Code 837305005054, Manufactured by Sweet's Candy Company, Salt Lake City, UT; 2) 4 oz., Gable Box, PC Code 837305005733
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Drugs)·D-016-2013·2012-10-31

    Watson Recalls Necon 10/11 Tablets Due to Potential HCTZ Contamination

    Watson Laboratories is recalling specific lots of Necon 10/11 oral contraceptives because they may contain trace amounts of Hydrochlorothiazide (HCTZ).

    Product
    Necon 10/11 (norethindrone and ethinyl estradiol) Tablets USP, 0.5 mg/35 mcg, 1 mg/35 mcg, inert tablets, 28-count tablets per dispenser packaged in 6 Tablet Dispensers per carton, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA; Distributed by: Watson…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0140-2013·2012-10-31

    DePuy Mitek Recalls SpiraLok Anchors Due to Post-Operative Fracture

    DePuy Mitek is recalling 1,315 units of SpiraLok 5.0mm anchors because they may fracture after surgery, requiring patients to undergo revision procedures.

    Product
    SpiraLok 5.0mm with Ethibond and needles Product Number: 222960 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0155-2013·2012-10-31

    DePuy Mitek Recalls SpiraLok Anchors Due to Post-Operative Fracture

    DePuy Mitek is recalling 4,321 units of SpiraLok 6.5 anchors because they may fracture after surgery, requiring revision. The recall covers worldwide distribution.

    Product
    SpiraLok 6.5 w/out Needles with violet and blue Orthocord Product Number: 222988 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0151-2013·2012-10-31

    DePuy Mitek Recalls SpiraLok 6.5 Anchors Due to Post-Operative Fracture

    DePuy Mitek is recalling SpiraLok 6.5 anchors because they may fracture after surgery, requiring patients to undergo revision procedures.

    Product
    SpiraLok 6.5 w/out Needles with Orthocord Product Number: 222971 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-027-2013·2012-10-31

    Raritan Pharmaceuticals Recalls Wal-Mucil Plus Calcium Fiber Capsules

    Raritan Pharmaceuticals is recalling Wal-Mucil Plus Calcium Fiber Capsules due to possible C. difficile contamination found in raw materials.

    Product
    Wal-Mucil Plus Calcium Fiber Capsules,100% Natural Fiber, 100% Natural Psyllium Seed Husk, Calcium/Dietary Fiber Supplement, 240 Capsules per bottle, Distributed by: Walgreen Co., 200 Wilmot Road, Deerfield, IL 60015-4616 www.walgreens.com, NDC 0363-0128-24, UPC 3-11917-07656-0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0150-2013·2012-10-31

    DePuy Mitek Recalls Seven SpiraLok 6.5 Anchors Due to Fracture Risk

    DePuy Mitek is recalling seven SpiraLok 6.5 anchors because they fractured after surgery, requiring patients to undergo revision procedures.

    Product
    SpiraLok 6.5 w/Needles with Orthocord Product Number: 222970 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0419-2013·2012-10-31

    Sunland Recalls Organic Peanut Butter for Potential Salmonella Contamination

    Sunland, Inc. is recalling Archer Farms Organic Chunky Peanut Butter because the product may be contaminated with Salmonella.

    Product
    Archer Farms Organic Chunky Peanut Butter, 12 oz, UPC 085239020302. Labeling is green, red, and yellow with white and black print writing. Manufactured for Target Corporation Minneapolis, MN 55403.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0319-2013·2012-10-31

    Buitoni Spinach Ravioli Recalled for Undeclared Shrimp and Lobster Allergens

    Nestle Prepared Foods is recalling Buitoni Spinach & Portobello Mushroom Ravioli because it may contain undeclared shrimp and lobster.

    Product
    BUITONI brand Spinach & Portobello Mushroom All Natural Ravioli, packaged in an 18 oz. bag, frozen UPC code 24842-99186
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0316-2013·2012-10-31

    Peach Brandy Jam Recalled for Undeclared Milk and Soy Allergens

    Hanover Pike Enterprises is recalling Peach Brandy Jam because it contains undeclared milk and soy ingredients.

    Product
    Peach Brandy Jam, 4 and 9 ounce jars, labeled in part ***Jill's Jams & Jellies, Hampstead, MD 21074***
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Food)·F-0308-2013·2012-10-31

    Jer's Chocolates Recalls Peanut Butter Bars Due to Salmonella Risk

    Jer's Chocolates is recalling specific Peanut Butter Bars and Squares because the peanut butter supplier, Sunland, Inc., recalled its products due to potential Salmonella contamination.

    Product
    Peanut Butter Bars Original: 3.0 oz, Two-Bar Box, UPC Code 837305005023, Manufactured by Sweet's Candy Company, Salt Lake City, UT; 2) 1.5 oz, One-Bar Box, UPC Code 837305006235; 3) .45 oz, Change Makers, UPC Code 837305005832; 4) 4 oz., Gable Box, UPC Code 837305005795
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Drugs)·D-030-2013·2012-10-31

    Raritan Pharmaceuticals Recalls Premier Value Fiber Capsules Due to C. Difficile Contamination

    Raritan Pharmaceuticals is recalling Premier Value Fiber Capsules due to possible C. difficile contamination found in the raw material.

    Product
    Premier Value Fiber Capsules, Fiber Capsules, 100% Natural Psyllium Fiber, Relieves Constipation, Restores Regularity, 160 Capsules per bottle, Distributed by: Chain Drug Consortium, LLC, Boca Raton, FL 33431, UPC0-40986-01703-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0333-2013·2012-10-31

    Sunland Recalls Peanut Butter Products Due to Salmonella Contamination Risk

    Sunland, Inc. is voluntarily recalling specific peanut butter products because they may be contaminated with Salmonella.

    Product
    Fresh and Easy Creamy Peanut Butter, packed in 18 oz, UPC 20003364 and 6/2 oz, UPC 5051379032494 and 40 oz, UPC 51379026431; labeling is blue, yellow and white with yellow, white, and black print writing. Produced for Fresh and Easy Neighborhood Market Inc, El Segundo, CA…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-033-2013·2012-10-31

    Mylan Recalls Doxazosin Tablets Due to Acetaminophen and Codeine Contamination

    Mylan Pharmaceuticals is recalling 24,331 bottles of Doxazosin Tablets, USP, 2 mg, due to cross-contamination with acetaminophen and codeine.

    Product
    Doxazosin Tablets, USP, 2 mg, 100 count bottles, labeled in part ***Manufactured in Australia by: ALPHAPHARM PTY LTD, 15 Garnet Street***Rx Only*** Carole Park QLD 4300, Australia*** Manufactured for Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.SA ***
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0070-2013·2012-10-31

    Hospira Symbiq Infusion Pump Recalled for Touchscreen Malfunctions

    Hospira is recalling Symbiq Two Channel Infusers because the touchscreen may fail to respond or register incorrect values, potentially causing medication delivery errors.

    Product
    Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids; Hospira, Inc., Lake Forest, IL 60045 USA, Made in Costa Rica; List Number 16027-01 Device is a general purpose infusion pump designed to deliver fluids, solutions, medications…
    Category
    Medical Device
    Distribution
    Distributed nationwide