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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Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

16226–16250 of 18042

  • LowFDA (Drugs)·D-394-2014·2014-01-08

    Qualitest Recalls Cetirizine Hydrochloride Syrup Due to Impurity Failure

    Qualitest Pharmaceuticals is recalling 438,055 bottles of Cetirizine Hydrochloride Syrup because the product failed impurity specifications for 4-chlorobenzophenone.

    Product
    Cetirizine Hydrochloride Syrup (Cetirizine Hydrochloride Oral Solution, USP) 1 mg/mL, 120 mL and 480 mL bottles, Rx only. Mfg. for: Qualitest Pharmaceuticals, Huntsville, AL 35811. NDC 0603-9063-54 (120 mL), NDC 0603-9063-58 (480 mL).
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-391-2014·2014-01-08

    G & W Fluocinolone Acetonide Cream Recalled for Content Uniformity Failure

    G & W Laboratories is recalling Fluocinolone Acetonide Cream 0.025% because it failed content uniformity specifications at the 18-month time point.

    Product
    FLUOCINOLONE ACETONIDE — FLUOCINOLONE ACETONIDE (FLUOCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-388-2014·2014-01-01

    GlaxoSmithKline Recalls Sumatriptan Injection Cartridges Due to Sterility Concerns

    GlaxoSmithKline is recalling 9,743 cartridges of Sumatriptan Succinate Injection because some may have needles protruding through the shield, compromising sterility.

    Product
    Sumatriptan Succinate Injection, 6 mg, 0.5 mL For subcutaneous injection only, Rx only, 2 Single-Dose Syringe Cartridges for use with sumatriptan Autoinjector Pen, Manufactured by GlaxoSmithKline, Research Triangle Park, NC 27709 for Sandoz Inc., Princeton, NJ 08540, Made in…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-387-2014·2014-01-01

    FDA Recalls Imitrex STATdose Systems Due to Sterility Concerns

    GlaxoSmithKline is recalling 10,469 Imitrex STATdose Systems because some syringes may have needles protruding through the shield, compromising sterility.

    Product
    IMITREX — IMITREX (SUMATRIPTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-390-2014·2014-01-01

    Physicians Total Care Recalls Carisoprodol Tablets Due to Foreign Substance

    Physicians Total Care is recalling Carisoprodol 350mg tablets because heavy metals and inactive components were found during routine stability testing.

    Product
    Carisoprodol IV ( Carisoprodol Tablets USP) 350mg, RX only. Mfd by: Shasun Chemicals Drugs LTD, Pondicherry, INDIA. Repacked and Distributed by: Physicians Total Care, Inc., Tulsa, OK 74146. 90 count bottle: NDC: 54868-0816-8, 60 count bottle: NDC: 54868-0816-4, 30 count…
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-384-2014·2014-01-01

    Tower Pharmacy Recalls Phenylephrine Nasal Spray Due to Microbial Contamination

    Tower Pharmacy is recalling Phenylephrine Nasal Spray 1% due to possible microbial contamination. The affected product is for office use and was distributed in California.

    Product
    Phenylephrine Nasal 1% Spray, 480 mL bottles, For Office Use, Tower Pharmacy, 26732 Crown Valley Pkwy, Suite 101, Mission Viejo, CA 92691
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-386-2014·2014-01-01

    Airgas Recalls 145 Compressed Oxygen Cylinders Due to Short Fill Error

    Airgas Medical Services is recalling 145 compressed oxygen cylinders that may be empty due to a manufacturing error. The cylinders were distributed to medical facilities in four states.

    Product
    Oxygen, Compressed USP, in an aluminum cylinder, Rx only, Airgas USA, LLC, Radnor PA 19087 Distributed by Keene Medical Products, 240 Meridian Road, NH 03766. NDC 11054-009
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-385-2014·2014-01-01

    Amedra Recalls Dexedrine Capsules Due to Dissolution Test Failures

    Amedra Pharmaceuticals is recalling 10,992 bottles of Dexedrine Spansules 15mg due to failed dissolution specifications at the 32-month stability level.

    Product
    Dexedrine¿ (Dextroamphetamine Sulfate) Spansules¿ Sustained Release Capsules 15mg, 90 count bottle, Rx only, Manufactured by Catalent Pharma Solutions Winchester, KY 40391 for Amedra Pharmaceuticals, LLC Middlesex, NJ 08846, NDC 52054-514-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-382-2014·2014-01-01

    Teva Recalls Qnasl Nasal Aerosol Due to Potential Clogged Stem Valves

    Teva Pharmaceuticals USA is recalling Qnasl Nasal Aerosol units because some may have clogged stem valves, potentially affecting delivery.

    Product
    Qnasl (beclomethasone dipropionate) Nasal Aerosol, 80 mcg per spray, 120 metered sprays, 8.7 g inhaler, Rx only, Manufactured for Teva Respiratory, LLC, Horsham, PA 19044; By: 3M Delivery Systems, Northridge, CA 91324, NDC 59310-210-12, UPC 3 59310 21012 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-389-2014·2014-01-01

    Hi-Tech Pharmacal Recalls Acyclovir Oral Suspension for Stability Failures

    Hi-Tech Pharmacal is recalling Acyclovir Oral Suspension because the product's viscosity and pH levels fell below required specifications.

    Product
    Acyclovir Oral Suspension, USP 200 mg/5 mL, Net Wt. 16 fl oz (473 mL), Rx only, Hi-Tech Pharmacal Co, Inc. Amityville, NY 11701. NDC 50383-810-16.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-376-2014·2013-12-25

    Evil Root 1200 mg Recalled for Undeclared Sildenafil

    Fabscout Entertainment, Inc. is recalling Evil Root 1200 mg capsules because the product contains undeclared sildenafil and was marketed without FDA approval.

    Product
    Evil Root 1200 mg, supplied in 6 capsules per bottle, Manufacturer: Tibet Shengyang Health Medicine Co.,Ltd. Address: No. 98, Min zu Road, Lhasa
    Category
    Drug
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-378-2014·2013-12-25

    PRO POWER MAX Energy Capsules Recalled for Undeclared Sildenafil and Tadalafil

    Fabscout Entertainment is recalling PRO POWER MAX Natural Energy Enhancer capsules because they contain undeclared sildenafil and tadalafil and were marketed without FDA approval.

    Product
    PRO POWER MAX Natural Energy Enhancer, ALL NATURAL HERBS, supplied in 1 capsule per blister pack, Distributed by MSH Distribution LLC
    Category
    Drug
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-370-2014·2013-12-25

    Zi Xiu Tang Ultimate Formula Recalled for Undeclared Sibutramine

    Zi Xiu Tang Success, LLC is recalling Ultimate Formula capsules because they contain undeclared sibutramine, an ingredient removed from the market for safety reasons.

    Product
    Ultimate Formula, Net Wt. 250 mg, 48 capsules per bottle, Distributed by: Zi Xiu Tang Success, LLC., Trexlertown, PA 18087, UPC 7 9357304140 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-371-2014·2013-12-25

    Quick Thin capsules recalled for containing unapproved drugs

    Bethel Nutritional Consulting is recalling Quick Thin capsules because FDA analysis detected unapproved drugs sibutramine and phenolphthalein.

    Product
    Quick Thin (citrus aurantium extract, sweet potato fiber, cyamopsis gum powder, alfalfa, mulberry leaf, guarana, spirulina) capsules, 400 mg, 30-count bottle, Distributed by: Bethel, Inc., Tel: (212) 568-5330.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-381-2014·2013-12-25

    Hospira Recalls Bupivacaine Hydrochloride Injection Due to Particulate Matter

    Hospira Inc. is recalling 119,600 vials of Bupivacaine Hydrochloride Injection due to the presence of visible particulate matter.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-377-2014·2013-12-25

    Dietary Supplement Recalled for Undeclared Sildenafil and Lack of FDA Approval

    Fabscout Entertainment is recalling 72HP Maximum Potency Male Sexual Enhancement because it contains undeclared sildenafil and was marketed without FDA approval.

    Product
    72HP MAXIMUM POTENCY MALE SEXUAL ENHANCEMENT, Dietary Supplement, supplied in 1 capsule per blister pack, Distributed by: 72HP, Inc. Weston, FL
    Category
    Drug
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-373-2014·2013-12-25

    Purity First B-50 Capsules Recalled for Undeclared Steroids

    Healthy Life Chemistry is recalling B-50 capsules because FDA analysis found undeclared steroids, making the product an unapproved new drug.

    Product
    B-50 capsules, 100-count bottles, labeled in part as Healthy Life Chemistry, By Purity First, Manufactured for: Purity First Health Products, Inc. Healthy Life Chemistry 51 Florida Street, Farmingdale, NY 11735; 1-800-696-7017
    Category
    Drug
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-369-2014·2013-12-25

    Bee Pollen Capsules Recalled for Undeclared Sibutramine

    Zi Xiu Tang Success, LLC is recalling Classic Zi Xiu Tang Bee Pollen Capsules because they contain undeclared sibutramine, an unapproved active ingredient.

    Product
    Classic Zi Xiu Tang, Bee Pollen Capsule, Net Wt. 250 mg x 60 capsules per bottle, Distributed by: Zi Xiu Tang Success, LLC., Trexlertown, PA 18087, UPC 6 937000 700019
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-380-2014·2013-12-25

    Hospira Recalls Bupivacaine Hydrochloride Injection Due to Particulate Matter

    Hospira Inc. is recalling 118,100 vials of 0.25% Bupivacaine Hydrochloride Injection due to the presence of visible particulate matter.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-375-2014·2013-12-25

    Altaire Recalls Carboxymethylcellulose Sodium Eye Drops Due to Non-Sterility

    Altaire Pharmaceuticals is recalling specific lots of Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution because the preservative may not be effective through expiry, posing a non-sterility risk.

    Product
    Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution, 1 FL OZ (30 mL) bottle, sold under the following labels: (a) CVS pharmacy brand LUBRICANT EYE DROPS FOR MILD TO MODERATE DRY EYE, Distributed by CVS Pharmacy, Inc., Woonsocket, RI 02895, UPC 0 50428 053357 7 and UPC 0 50428…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-372-2014·2013-12-25

    Bethel Advance capsules recalled for unapproved drug ingredients

    Bethel Nutritional Consulting is recalling Bethel Advance capsules because FDA analysis detected unapproved drug ingredients, including phenolphthalein and sibutramine.

    Product
    Bethel Advance (bitter orange, mulberry leaf, cassia seed extract, jobstear seed, spirulina, starch, kola nut) capsules, 400 mg, 30-count bottles, Distributed by: Bethel, Inc., Tel: (212) 568-5330, UPC 1 60126 41750 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-374-2014·2013-12-25

    Purity First Recalls Multi-Mineral Capsules for Undeclared Steroids

    Healthy Life Chemistry is recalling multi-mineral capsules because they contain undeclared steroid-like substances, making them unapproved new drugs.

    Product
    Multi-Mineral capsules, 200-count bottles, labeled in part as Healthy Life Chemistry, By Purity First, Manufactured for: Purity First Health Products, Inc. Healthy Life Chemistry 51 Florida Street, Farmingdale, NY 11735; 1-800-696-7017
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Drugs)·D-367-2014·2013-12-25

    West-Ward Recalls Carisoprodol Tablets Due to Foreign Substance Presence

    West-Ward Pharmaceutical Corp. is recalling 20,534 bottles of Carisoprodol Tablets, USP 350 mg, because heavy metals and inactive components were visually observed during routine stability testing.

    Product
    Carisoprodol Tablets, USP 350 mg, Rx Only, 1000 tablets. Dist by: West-ward Pharmaceutical Corp. Eatontown, NJ 07724. Mfd by: Shasun Chemicals and Drugs Limited, Unit II, R. S. Na 32, 33, 743 PIMS Rd, Periyakalepet, Pondicherry. 605014 INDIA. NDC 0143-9749-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-368-2014·2013-12-25

    Baxter Recalls Travasol Amino Acid Injection Due to Sterility Concerns

    Baxter Healthcare is recalling 14,622 bags of Travasol Amino Acid Injection because leaking containers prevent assurance of sterility.

    Product
    TRAVASOL — TRAVASOL (LEUCINE, PHENYLALANINE, LYSINE HYDROCHLORIDE, METHIONINE, ISOLEUCINE, VALINE, HISTIDINE, THREONINE, TRYPTOPHAN, ALANINE, GLYCINE, ARGININE, PROLINE, TYROSINE, SERINE)
    Category
    Drug
    Distribution
    Distributed nationwide