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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32176–32200 of 39756

  • SevereFDA (Drugs)·D-620-2014·2014-01-22

    FDA Recalls Tizanidine Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Tizanidine HCl tablets that may be mislabeled as Pyridoxine HCl. The error could lead to patients taking the wrong medication.

    Product
    tiZANidine HCl Tablet, 1 mg (1/2 of 2 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 55111017915
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-653-2014·2014-01-22

    Aidapak Recalls Vitamin B Complex Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling Vitamin B Complex with C/Folic Acid tablets because they may be mislabeled as other prescription or over-the-counter medications.

    Product
    VITAMIN B COMPLEX WITH C/FOLIC ACID, Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258016001
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-425-2014·2014-01-22

    Hyaluronidase Recalled Due to Lack of Assurance of Sterility

    Specialty Medicine Compounding Pharmacy is recalling Hyaluronidase products because sterility cannot be assured after a related product was found non-sterile.

    Product
    Hyaluronidase, pf 100U/mL; pf 150 U/mL, Rx only, Specialty Medicine Compounding Pharmacy, 350 S Lafayette, South Lyon, MI 48178
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-447-2014·2014-01-22

    Specialty Medicine Compounding Pharmacy Recalls Hydroxyprogesterone Injectable Due to Sterility Concerns

    Specialty Medicine Compounding Pharmacy is recalling Hydroxyprogesterone 17alpha-PF 250 mg/mL injectable because sterility cannot be assured after a related product was found non-sterile.

    Product
    HYDROXYPROGEST*-17ALPHA -PF 250 mg/mL INJECTABLE, Rx only, Specialty Medicine Compounding Pharmacy, 350 S Lafayette, South Lyon, MI 48178
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-526-2014·2014-01-22

    FDA Recalls Mislabeled HydrALAZINE Tablets Due to Label Mixup

    Aidapak Services is recalling HydrALAZINE HCl tablets because they may be mislabeled as other prescription drugs. The recall covers repacked drugs distributed in four western states.

    Product
    hydrALAZINE HCl Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155000401
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Food)·F-1417-2014·2014-01-22

    Fosforel Herring Fillets Recalled Due to Listeria monocytogenes Presence

    Zip International Group LLC is recalling Fosforel Atlantika Herring Fillets in Oil after Listeria monocytogenes was detected in samples.

    Product
    Fosforel Atlantika Herring Fillet in Oil (200 g) Product of Russia Imported by: Zip International Group LLC 160 Raritan Center Parkway, Unit 6 Edison, NJ 08837 UPC: 4607106577526
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-457-2014·2014-01-22

    Calcium Chloride Injection Recalled Due to Sterility Assurance Concerns

    Specialty Medicine Compounding Pharmacy is recalling Calcium Chloride PF 500 mg/mL prefilled syringes because sterility cannot be assured after a related product was found non-sterile.

    Product
    Calcium Chloride* PF 500 mg/mL pref syringe, Rx only, Specialty Medicine Compounding Pharmacy, 350 S Lafayette, South Lyon, MI 48178
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1399-2014·2014-01-22

    Jensen's Recalls Hot Smoked Salmon Due to Botulism Risk

    Jensen's Old Fashioned Smokehouse is recalling Jack's Fish Spot Hot Smoked Cajun Atlantic Salmon because it may lack 'KEEP FROZEN' labeling, posing a risk of Clostridium botulinum contamination.

    Product
    Jack's Fish Spot Hot Smoked Cajun Atlantic is a low salt, vacuum packaged, Hot Smoked Salmon. This product is labeled in parts: "***Hot Smoked Atlantic Salmon*** INGREDIENTS: Atlantic Salmon, Salt, Brown Sugar, Spices and Natural Wood Smoke***Important: Keep Frozen. Thaw…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-632-2014·2014-01-22

    FDA Recalls Pimozide Tablets Due to Potential Metoprolol Labeling Error

    Aidapak Services is recalling Pimozide 1 mg tablets that may be mislabeled as Metoprolol Tartrate 12.5 mg. The error poses a risk of incorrect medication administration.

    Product
    PIMOZIDE Tablet, 1 mg (1/2 of 2 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 57844018701
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Food)·F-1404-2014·2014-01-22

    Concertos In Chocolate Recalls Solid Milk Chocolate Santa Candy

    Concertos In Chocolate LLC is recalling Solid Milk Chocolate Santa candy because it is incorrectly labeled and contains an undeclared milk allergen.

    Product
    SOLID MILK CHOCOLATE SANTA candy
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-2011-2014·2014-01-22

    Big Blue Fisheries Recalls Smoked Coho Salmon Due to Botulism Risk

    Big Blue Fisheries is recalling all smoked products because they may not have been properly cooked, posing a risk of Clostridium botulinum contamination.

    Product
    Hickory Smoked Coho Salmon is sold in vacuum packed plastic packages, net weight from 0.5 to 1 lb., with label located on the front that include the pack date and AK 604. The label is read in parts: "***BIG BLUE FISHERIES, LLC***Hickory Smoked Coho Salmon***Ingredients: Wild…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-444-2014·2014-01-22

    Sodium Phosphate Injectable Recalled Due to Sterility Concerns

    Specialty Medicine Compounding Pharmacy is recalling Sodium Phosphate injectable products because sterility cannot be assured after a related product was found non-sterile.

    Product
    SODIUM PHOSPHATE* PF 3MMOL/mL INJECTABLE, SODIUM PHOSPHATE* PF(15 mL) 3MMOL/mL INJECTABLE, Rx only, Specialty Medicine Compounding Pharmacy, 350 S Lafayette, South Lyon, MI 48178
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-446-2014·2014-01-22

    Sodium Thiosulfate Injectable Recalled for Lack of Sterility Assurance

    Specialty Medicine Compounding Pharmacy is recalling Sodium Thiosulfate PF, 10% injectable, because sterility cannot be assured after another product was found non-sterile in the same environment.

    Product
    Sodium Thiosulfate PF, 10 % injectable, Rx only, Specialty Medicine Compounding Pharmacy, 350 S Lafayette, South Lyon, MI 48178
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-484-2014·2014-01-22

    FDA Recalls Glucosamine/Chondroitin Tablets Due to Potential Label Mixup

    Aidapak Services is recalling Glucosamine/Chondroitin DS tablets because they may be mislabeled as Docusate Sodium capsules. The error could lead to patients taking the wrong medication.

    Product
    GLUCOSAMINE/CHONDROITIN DS, Tablet, 500 mg/400 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904559293
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Food)·F-1390-2014·2014-01-22

    Jensen's Recalls Hot Smoked Sturgeon Due to Botulism Risk

    Jensen's Old Fashioned Smokehouse is recalling hot smoked sturgeon because inconsistent 'KEEP FROZEN' labeling creates a risk of Clostridium botulinum contamination.

    Product
    Low salt, vacuum packaged, Hot Smoked Sturgeon Clippership product is labeled in parts: "***Keep Frozen. Thaw under refrigeration immediately before use***".
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-456-2014·2014-01-22

    Specialty Medicine Compounding Pharmacy Recalls WB-Tranexamic Acid Due to Sterility Concerns

    Specialty Medicine Compounding Pharmacy is recalling WB-Tranexamic acid products because sterility cannot be assured after a related product was found to be non-sterile.

    Product
    WB-Tranexamic acid, 2 g/Placebo 100 mL, DRUG STUDY, packaged as a) 100 mL INJECTABLE, b) TOPICAL, Rx only, Specialty Medicine Compounding Pharmacy, 350 S Lafayette, South Lyon, MI 48178
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-460-2014·2014-01-22

    Sodium Hydroxide Solution Recalled Due to Sterility Concerns

    Specialty Medicine Compounding Pharmacy is recalling Sodium Hydroxide 10% Solution because sterility cannot be assured after a related product was found non-sterile.

    Product
    SODIUM HYDROXIDE (BAC.STATIC) 10% SOLUTION, Rx only, Specialty Medicine Compounding Pharmacy, 350 S Lafayette, South Lyon, MI 48178
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·14E002000·2014-01-17

    B&W Recalls Tow & Stow Adjustable Ball Mounts Due to Pin Fracture Risk

    B&W Custom Truck Beds is recalling specific Tow & Stow Adjustable Ball Mounts because the securing pins may fracture, potentially causing the trailer to separate from the vehicle.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·005-2014·2014-01-17

    Gusto Packing Recalls Sliced Spiral Hams for Possible Listeria Contamination

    Gusto Packing is recalling approximately 67,113 pounds of sliced spiral ham products due to possible Listeria monocytogenes contamination. The products were distributed in Illinois, Indiana, Kentucky, Ohio, and Canada.

    Product
    Carl Buddig and Company — Illinois Firm Recalls Sliced Spiral Hams for Possible Listeria Contamination
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·14V010000·2014-01-16

    Aston Martin Recalls Multiple Models Due to Accelerator Pedal Arm Defect

    Aston Martin is recalling specific 2008-2014 models because a manufacturing error may cause the accelerator pedal arm to break, preventing the driver from maintaining or increasing engine speed.

    Product
    ASTON MARTIN — ASTON MARTIN V8 VANTAGE S, RAPIDE S, V12 VANTAGE COUPE, DB9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0650-2014·2014-01-15

    Nova Hospital Blood Glucose Meters Recalled for Battery Swelling and Leakage

    Nova Biomedical is recalling hospital blood glucose meters due to battery swelling and cell leakage. The recall covers approximately 200,000 units distributed nationwide.

    Product
    Nova StatStrip/StatSensor Hospital Blood Glucose Meter; Nova StatStrip Lactate Hospital Meter System; Nova StatSensor Creatinine Hospital Meter, Rechargeable Lithium Batteries Single: 46626; 4 Pack: 46827; 5 Pack: 50436. For Point-Of-Care usage in the quantitative…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0654-2014·2014-01-15

    Anspach Pneumatic Drill System Recalled Due to Hose Rupture Risk

    The Anspach Effort, Inc. is voluntarily removing Pneumatic Drill Systems from the market because the outer hose on the motor hand-piece can rupture without warning if air flow is blocked.

    Product
    ***REF BLACKMAX-N***Swivel/Angle Motor Assembly***Rx Only***The Anspach Effort, Inc. Intended for cutting and shaping bone.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1645-2013·2014-01-15

    Creole Bisque Recalled for Undeclared Milk, Soy, and Wheat Allergens

    Creole & Company is recalling Creole Bisque because it contains milk, soy, and wheat without an ingredient statement declaring their presence.

    Product
    Creole & Company Creole Bisque, NET WEIGHT 3.47 oz (98g), manufacture for: Creole & Company, 145 Robert E. Lee Blvd. Penthouse Suite, New Orleans, LA 70124, UPC: 811773014869
    Category
    Food
    Distribution
    1 state