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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17451–17475 of 18009

  • ModerateFDA (Drugs)·D-224-2013·2013-04-03

    CareFusion Recalls Misbranded Isopropanol Applicators Due to Sterility Labeling

    CareFusion 213, LLC is recalling 698,000 SEPP 70% Isopropanol applicators because the product is not sterile, making the labeling misleading regarding sterility claims.

    Product
    SEPP 70% Isopropanol (isopropyl alcohol) 70% v/v, USP, 200-count applicators (net 0.67 mL each) per carton, Cat. No 260201, NDC 54365-170-01, CareFusion, Leawood, KS 66211.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-218-2013·2013-04-03

    Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil

    Hill Dermaceuticals is recalling 8,592 bottles of Derma-Smoothe/FS topical oil because the product was found to be subpotent at a 22-month stability timepoint.

    Product
    Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical Oil(SCALP OIL), Rx only, FOR TOPICAL USE ONLY, NOT FOR ORAL, OPHTHALMIC, OR INTRAVAGINAL USE, Net Contents 118.28 mL (4 fl. oz.), Hill Dermaceuticals, Inc., Sanford, Florida --- NDC 28105-149-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-222-2013·2013-04-03

    Physicians Total Care Tetracycline Recalled for Potential Foreign Particulate Matter

    Physicians Total Care is recalling Tetracycline 500 mg capsules due to a potential for foreign particulate matter in the active pharmaceutical ingredient.

    Product
    PHYSICIANS TOTAL CARE, TETRACYCLINE, 500 mg, 30 CAPSULES, bottle MFG. BY: TEVA PHARMACEUTICALS USA, SELLERSVILLE PA 18960 NDC 54868-0025-09
    Category
    Drug
    Distribution
    10 states
  • ModerateFDA (Drugs)·D-220-2013·2013-04-03

    Ciprofloxacin Tablets Recalled for Foreign Material Presence

    West-ward Pharmaceutical Corp. is recalling Ciprofloxacin 500 mg tablets due to a complaint of rubber-like material found in a tablet.

    Product
    CIPROFLOXACIN — CIPROFLOXACIN (CIPROFLOXACIN)
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-227-2013·2013-04-03

    CareFusion Blood Culture Prep Kits Recalled for Misleading Sterility Labeling

    CareFusion is recalling Blood Culture Prep Kit II units because the product is not sterile, making the labeling misleading regarding sterility claims.

    Product
    Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol), Net 1.1 mL and 1 SEPP (iodine tincture 2% USP), Net 0.67 mL per kit, packaged in 20-count kits per carton, Cat. No 260307, NDC 54365-200-99, CareFusion, Leawood, KS 66211.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-221-2013·2013-04-03

    Physicians Total Care Tetracycline Recalled for Potential Foreign Particulate Matter

    Physicians Total Care is recalling Tetracycline 250 mg capsules due to a potential for foreign particulate matter in the active pharmaceutical ingredient.

    Product
    PHYSICIANS TOTAL CARE, TETRACYCLINE, 250 mg, 30 CAPSULES, bottle MFG. BY: TEVA PHARMACEUTICALS USA, SELLERSVILLE PA 18960 NDC 54868-0024-08
    Category
    Drug
    Distribution
    10 states
  • ModerateFDA (Drugs)·D-226-2013·2013-04-03

    CareFusion Recalls Povidone Iodine Applicators Due to Sterility Labeling Errors

    CareFusion is recalling SEPP 10% Povidone Iodine Solution applicators because the product is not sterile, making the sterility claims on the label misleading.

    Product
    SEPP 10% Povidone Iodine Solution USP (1% available Iodine, Surfactant & USP Purified Water), packaged in a) 200-count applicators (Net 0.67 mL each) per carton, CareFusion, Leawood, KS 66211, Cat. No 260286, NDC 54365-145-01; and b) 3000-count applicators per case, Cat. No…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-228-2013·2013-04-03

    CareFusion Recalls Donor Prep Kits Due to Misleading Sterility Labeling

    CareFusion 213, LLC is recalling 46,500 Donor Prep Kits because the labeling is misleading regarding sterility claims. The product is not sterile.

    Product
    Donor Prep Kit containing 1 FREPP (70% isopropyl alcohol), Net 1.1 mL and 1 SEPP (iodine tincture 2% USP), Net 0.67 mL per kit, packaged in 20-count kits per carton, Cat. No 260311, NDC 54365-201-99, CareFusion, Leawood, KS 66211.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-225-2013·2013-04-03

    CareFusion Recalls SEPP 2% Iodine Tincture Applicators for Sterility Mislabeling

    CareFusion 213, LLC is recalling SEPP 2% Iodine Tincture applicators because the product is not sterile, making the labeling misleading regarding sterility claims.

    Product
    SEPP 2% Iodine Tincture USP (47% v/v Ethyl Alcohol, 2% w/v Iodine, USP, Sodium Iodide USP, & Purified Water USP), packaged in a) 200-count applicators (Net 0.67 mL each) per carton, Cat. No 260261, NDC 54365-161-01, CareFusion, Leawood, KS 66211; b) 3000-count applicators (Net…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-217-2013·2013-04-03

    Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil

    Hill Dermaceuticals is recalling 8,736 bottles of Derma-Smoothe/FS topical oil because the product was found to be subpotent at the 12-month stability timepoint.

    Product
    Derma-Smoothe/FS (fluocinolone acetonide), 0.01% Topical Oil (Body Oil), Rx only, Hill Dermaceuticals, Inc., Sanford, Florida 32773 --- NDC 28105-150-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-219-2013·2013-04-03

    Pfizer Recalls TORISEL Kits Due to Sterility and Endotoxin Concerns

    Pfizer is recalling 10,920 TORISEL (temsirolimus) kits nationwide due to a lack of assurance of sterility and potential low-level endotoxins in the diluent vials.

    Product
    TORISEL — TORISEL (TEMSIROLIMUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-215-2013·2013-04-03

    Hospira Recalls Lactated Ringer's Injection Due to CGMP Deviations

    Hospira is recalling 1,296 units of Lactated Ringer's Injection, USP, 1000 mL, because the product was shipped without approval for release.

    Product
    Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Drugs)·D-216-2013·2013-04-03

    L. Perrigo Recalls Subpotent PE Daytime Cold/Flu LiqGel Blister Packs

    L. Perrigo is recalling 60,048 blister packs of PE Daytime Cold/Flu LiqGel because the active ingredient Phenylephrine HCl was subpotent at the 12-month time point.

    Product
    PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Phenylephrine HCL 325/10/5 mg gel caps 20 count blister pack, Distributed By: Wal-Mat Stores Inc., Bentonville, AR, 72716
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-214-2013·2013-03-27

    Physicians Total Care Recalls Subpotent Levothyroxine Tablets

    Physicians Total Care is recalling Levothyroxine Tablets, USP, 0.175 mg, due to subpotency and stability issues. The recall affects specific lots distributed in Ohio and Georgia.

    Product
    Levothyroxine Tablets, USP (levothyroxine sodium), 0.175 mg, 30 count bottles, Rx, Repacked & distributed by: Physicians Total Care, Inc., Tulsa, OK --- NDC 54868-4507-00
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-203-2013·2013-03-27

    Watson Recalls Meprobamate Tablets Due to Impurity Specification Failure

    Watson Laboratories is recalling meprobamate 200 mg tablets because an impurity, diphenyl sulfone, exceeded specification limits.

    Product
    Meprobamate, Tablets USP, 200 mg, 100 tablets; Rx only; Manufactured By: Watson Laboratories, Inc., Corona, CA 92800 USA; 173266; . Distributed by: Watson Pharma, Inc., NDC 9591-5239-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-206-2013·2013-03-27

    Hospira Recalls Metronidazole Injection Bags Due to Sterility Concerns

    Hospira Inc. is recalling 567,624 bags of Metronidazole Injection due to a potential leak that compromises sterility.

    Product
    METRONIDazole Injection, USP 500 mg (5 mg/mL), 100 mL Bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 (NDC 0409-7811-24)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-204-2013·2013-03-27

    Watson Recalls Meprobamate Tablets Due to Impurity Failure

    Watson Laboratories is recalling meprobamate 400 mg tablets because an impurity, diphenyl sulfone, exceeded specification limits.

    Product
    Meprobamate; Tablets USP, 400 mg, 100 tablets; Rx only; Manufactured By: Watson Laboratories, Inc., Corona, CA 92800 USA; 173266; . Distributed by: Watson Pharma, Inc., NDC 0591-5238-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-205-2013·2013-03-27

    Watson Recalls Zarah Oral Contraceptive Tablets Due to Breakage

    Watson Laboratories is recalling Zarah oral contraceptive tablets because they may break while being pushed through the blister pack.

    Product
    ZARAH¿ Drospirenone/ Ethinyl Estradiol Tablets, 3.0 mg/0.03 mg, Rx only, 3 tablet dispensers, 28 tablets each, Manuf. by: Watson Laboratories, Inc., Corona, CA 92880. USA; Distributed by: Watson Pharma, Inc., Corona, CA 92880 USA. NDC 52544-981-31 Carton; NDC 52544-981-28
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-207-2013·2013-03-27

    Novartis Recalls Myoflex Cream Due to Illegible Lot and Expiration Dates

    Novartis Consumer Health is recalling Myoflex Pain Relieving Cream because lot numbers and expiration dates may be illegible. The recall covers 2-oz and 4-oz tubes distributed nationwide and in Panama.

    Product
    Myoflex (trolamine salicylate) 10%, Pain Relieving Cream, a) 2-oz tube, b) 4-oz. tube, OTC. The firm name on the label is Novartis Consumer Health, Inc., Parsippany, NJ 07054.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-208-2013·2013-03-27

    Novartis Recalls Nupercainal Ointment Due to Illegible Labeling

    Novartis Consumer Health is recalling Nupercainal Ointment because lot numbers and expiration dates may be illegible or missing.

    Product
    Nupercainal, Dibucaine, Hemorrhoidal & Topical Analgesic Ointment, a) 1-oz. tubes (NDC 0067-5812-96), b) 2-oz. tubes (NDC 0067-5812-86), OTC. Distributed by Novartis Consumer Health, Inc., Parsippany, NJ 07054.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-209-2013·2013-03-27

    Novartis Recalls 4 Way Nasal Spray Due to Illegible Labeling

    Novartis Consumer Health is recalling 4 Way Nasal Spray because lot numbers and expiration dates may be illegible.

    Product
    4 WAY — 4 WAY (PHENYLEPHRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-210-2013·2013-03-27

    Novartis Recalls Nasal Spray Due to Illegible Lot and Expiration Dates

    Novartis Consumer Health is recalling 4 way Nasal Decongestant Menthol Nasal Spray because lot numbers and expiration dates may be illegible.

    Product
    4 way Nasal Decongestant Menthol Nasal Spray, containing phenylephrine hydrochloride 1%, a) 1/2-fl. oz. bottles (NDC 0067-2087-05) b) 1-fl. oz. bottles (NDC 0067-2087-01), OTC. Distributed by Novartis Consumer Health, Inc., Parsippany, NJ 07054.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-211-2013·2013-03-27

    Novartis Recalls 4 Way Saline Moisturizing Mist Due to Labeling Errors

    Novartis Consumer Health is recalling 4 Way Saline Moisturizing Mist bottles because lot numbers or expiration dates may be illegible or missing.

    Product
    4 way Saline Moisturizing Mist with Eucalyptol & Menthol, 1-fl. oz. bottles, OTC. Distributed by Novartis Consumer Health, Inc., Parsippany, NJ 07054.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-201-2013·2013-03-27

    West-ward Recalls Carisoprodol Tablets for Missing C-IV Labeling

    West-ward Pharmaceutical Corp. is recalling 1,763 bottles of Carisoprodol Tablets, 350 mg, because they lack the required C-IV imprint on the label.

    Product
    Carisoprodol Tablets, USP, 350 mg Rx Only, 100 tablets per bottle, Rx Only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724, NDC 0143-1176-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-191-2013·2013-03-20

    RX3 Pharmacy Recalls Medi-bolic Booster Injectable Due to Manufacturing Deviations

    RX3 Pharmacy is recalling 126 vials of Medi-bolic Booster Injectable because the product was not manufactured according to Good Manufacturing Procedures.

    Product
    Medi-bolic Booster Injectable (methionine 8.3 mg/mL, choline chloride 16.6 mg/mL, inositol 16.6 mg/mL, cyanocobalamin USP [Vit B12] 0.33 mg/mL, chromium chloride 2.6 mg/mL), 30 mL multi-dose vials, Rx3 Compounding Pharmacy, 12230 Ironbridge Rd., Suite C, Chester, VA 23831.
    Category
    Drug
    Distribution
    Distributed nationwide