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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8576–8593 of 8593

  • SevereFDA (Drugs)·D-1440-2012·2012-08-08

    VistaPharm Recalls Xactdose Phenytoin Oral Suspension Due to Container Defects

    VistaPharm is recalling Xactdose Phenytoin Oral Suspension because defective container lids allow moisture loss, potentially causing viscosity and assay failures.

    Product
    Xactdose Phenytoin Oral Suspension, USP 125 mg/5mL, supplied in 5 mL unit dose cups, VISTAPHARM, Largo, FL NDC 66689-036-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1429-2012·2012-08-08

    Eagle Pharmaceuticals Recalls Argatroban Injection Due to Visible Particulates

    Eagle Pharmaceuticals is recalling specific lots of Argatroban Injection after a hospital reported crystalline particulates and fibers in a vial.

    Product
    Argatroban Injection 50 mg per 50ml (1 mg per ml) For Intravenous Infusion Only, a) Single Use Vial (NDC 42367-203-07), b) 10 Single Use Vials(NDC 42367-203-84), Rx Only, Manufactured by: Cipla LTD, India, Manufactured for: Eagle Pharmaceuticals, Inc. Woodcliff Lake, NJ 07677
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1433-2012·2012-08-08

    Bayer Recalls Estradiol Hemihydrate Powder Due to Cross Contamination

    Bayer HealthCare Pharmaceuticals is recalling Estradiol Hemihydrate M20 EP/USP Powder due to cross contamination with another product. The affected lot was distributed in Kansas and California.

    Product
    Estradiol Hemihydrate M20 EP/USP Powder, packaged in a) 1.5 kg and b) 2.5 kg fiber drums, Rx only, Art. No. 165811, Bayer Pharma AG, D-13342 Berlin.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1434-2012·2012-08-08

    Dr. Reddy's Recalls Amlodipine and Benazepril Capsules Due to Foreign Tablets

    Dr. Reddy's is recalling Amlodipine Besylate and Benazepril Hydrochloride capsules because bottles were mislabeled and contained foreign Ciprofloxacin tablets.

    Product
    AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE — AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE (AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1425-2012·2012-08-01

    Grandpa Brands Recalls Dent's Extra Strength Toothache Gum

    Grandpa Brands Co is recalling Dent's Extra Strength Toothache Gum due to superpotent benzocaine levels. Consumers should stop using the product.

    Product
    Dent's Extra Strength Toothache Gum, (benzocaine 20%), Net Wt. .035 Oz.. (1 g) box, C.S. Dent & Co., Erlanger, KY
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1419-2012·2012-07-25

    Hospira Recalls Morphine Sulfate Injection Cartridges Due to Overfilling

    Hospira Inc. is recalling Morphine Sulfate Injection cartridges that contain 2.2 mL instead of the labeled 1 mL, posing a risk of overdose.

    Product
    Morphine Sulfate Injection, USP, 4mg/mL, 1 mL fill in 2.5 mL Carpuject Cartridge Unit with Luer Lock, packaged 10 Carpujects/carton, CII, Rx only, Hospira, Inc., Lake Forest, IL ---- NDC 0409-1258-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1421-2012·2012-07-25

    Luitpold Recalls Epinephrine Injection Ampules Due to Particulate Matter

    Luitpold Pharmaceuticals is recalling Epinephrine Injection ampules because of the presence of particulate matter. The affected lot was distributed nationwide.

    Product
    Epinephrine Injection, USP, 1:1000 (1 mg/mL), 25 x 1 mL Ampules, For SC and IM Use, For IV and IC Use after Dilution, Rx Only, American Regent, Inc., Shirely, NY 11967 --NDC 0517-1071-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1416-2012·2012-07-18

    VistaPharm Recalls Hydrocodone and Acetaminophen Oral Solution Due to Impurities

    VistaPharm is recalling specific lots of Hydrocodone Bitartrate & Acetaminophen Oral Solution because impurities exceeded specifications during stability testing.

    Product
    Hydrocodone Bitartrate & Acetaminophen Oral Solution 7.5 mg/325 mg per 15 mL, a) 15 mL Unit Dose Cups (50 unit dose cups per case), b) 473 mL Bottles, C III, Rx Only, Warning May be habit forming, Manufactured by VistaPharm, Largo, FL 33771, NDC a) 66689-023-50, b) NDC 66689-023-
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1412-2012·2012-07-18

    Trizivir Tablets Recalled Due to Potential Foreign Tablet Contamination

    GlaxoSmithKline is recalling Trizivir tablets because they may contain foreign Lexiva tablets. Patients should stop using the affected lot and contact their healthcare provider.

    Product
    Trizivir (abacavir sulfate 300mg, lamivudine 150 mg and zidovudine 300 mg), 60 Tablets, Rx only, Manufactured for: ViiV Healthcare, Research Triangle Park, NC 27709 by: GlaxoSmithKline, Research Triangle Park, NC 27709, NDC 49702-217-18
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1395-2012·2012-07-04

    Lloyd Inc Recalls Subpotent Thyro-Tab 0.75 mg Tablets

    Lloyd Inc is recalling 1,913,236 Thyro-Tab 0.75 mg tablets because they failed potency testing at the 6-month interval.

    Product
    Thyro-Tab.075 mg., packaged in bulk drums for repackaging. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, Iowa 51601.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1386-2012·2012-06-27

    Physicians Total Care Recalls Morphine Sulfate Tablets Due to Labeling Error

    Physicians Total Care is recalling Morphine Sulfate tablets because bottles may be mislabeled, potentially containing the wrong formulation.

    Product
    Morphine Sulfate Immediate Release tablet, 30 mg/120 tablet bottles, Rx only, Physician Total Care, Inc, Tulsa, OK 74146-6234, NDC 54868-4973-00
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1385-2012·2012-06-27

    Physicians Total Care Recalls Morphine Sulfate Extended Release Tablets Due to Labeling Error

    Physicians Total Care is recalling Morphine Sulfate Extended Release tablets because bottles may be mislabeled as Immediate Release or vice versa.

    Product
    Morphine Sulfate Extended Release tablet, 30 mg, 60 tablet bottles, Rx only, Physician Total Care, Inc, Tulsa, Ok 74146-6234, NDC 54868-4033-00
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1370-2012·2012-06-20

    Bausch & Lomb Recalls Murocel Lubricant Ophthalmic Solution Due to Sterility Concerns

    Bausch & Lomb is recalling 59,777 bottles of Murocel Lubricant Ophthalmic Solution because the product failed antimicrobial effectiveness testing.

    Product
    Murocel (methylcellulose) Lubricant Opthalmic Solution (USP, 1%), 15 mL bottle, OTC, Manufactured by Bausch & Lomb Incorporated, Tampa, FL 33637, NDC 24208-280-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1371-2012·2012-06-20

    Airgas Recalls Carbon Dioxide Medical Gas Cylinders Due to Impurities

    Airgas Inc is recalling 123 cylinders of Carbon Dioxide, USP, Medical Gas due to out-of-specification levels of nitrogen dioxide. The affected product was distributed to medical facilities in Arizona and California.

    Product
    Carbon Dioxide, USP, Medical Gas, packaged in a) size EA aluminum, CGA940 (CDUSPEA), b) size E CGA 940 (CDUSPE), c) 50 lb CGA320 (CDUSP50, CD USP50S), d) size 160 liter (CD USP160LT350) cylinders, Rx only, Airgas, Puritan Medical, Distributed By: Airgas USA, LLC, Radnor, PA.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1369-2012·2012-06-20

    Meridian Recalls Diazepam Autoinjectors Due to High Carbostyril Levels

    Meridian Medical Technologies is recalling 83,400 Diazepam autoinjectors because they contain high levels of carbostyril, a known degradation product.

    Product
    DIAZEPAM — DIAZEPAM (DIAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide