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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12326–12350 of 17987

  • SevereFDA (Drugs)·D-0788-2016·2016-04-06

    Walter's Pharmacy Recalls Lidocaine Nebulizer Solution Due to Sterility Concerns

    Walter's Pharmacy is recalling Lidocaine Nebulizer 2% Solution because the product lacks assurance of sterility. The recall affects 5 bottles distributed in Pennsylvania.

    Product
    Lidocaine Nebulizer 2% Solution, packaged in 50mL, 100mL, 120mL, and 150mL bottles, Rx only, Walter's Pharmacy, 401 N 17th St, Allentown, PA 610-435-4706, NDC 99999-9000-99
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0793-2016·2016-04-06

    Walter's Pharmacy Recalls Atropine Ophthalmic Solution Due to Sterility Concerns

    Walter's Pharmacy is recalling 22 bottles of Atropine 0.01% Ophthalmic Solution in Pennsylvania due to a lack of assurance of sterility.

    Product
    Atropine 0.01% Ophth Solution, 15mL bottle, Rx only, Walter's Pharmacy 401 N 17th St Allentown, PA 610-435-4706, NDC 99999-9019-09
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0787-2016·2016-04-06

    Walter's Pharmacy Recalls Edetate Disodium Eye Drops for Sterility Concerns

    Walter's Pharmacy is recalling 3 bottles of Edetate Disodium 3% Ophth Solution due to a lack of assurance of sterility. The product was distributed in Pennsylvania.

    Product
    Edetate Disodium 3% Ophth Solution, 10mL bottle, Rx only, Walter's Pharmacy, 401 N 17th St, Allentown, PA 610-435-4706, NDC 99999-9019-47
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0797-2016·2016-04-06

    Walter's Pharmacy Recalls Vancomycin Solution Due to Sterility Concerns

    Walter's Pharmacy is recalling Vancomycin 50mg/mL Solution because there is a lack of assurance of sterility. The recall affects 10mL bottles distributed in Pennsylvania.

    Product
    Vancomycin 50mg/mL Solution, 10mL bottle, Rx only, Walter's Pharmacy, 401 N 17th St, Allentown, PA 610-435-4706, NDC 99999-9991-54
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0792-2016·2016-04-06

    Walter's Pharmacy Recalls Vancomycin Solution Due to Sterility Concerns

    Walter's Pharmacy is recalling specific lots of Vancomycin 25mg/mL solution due to a lack of assurance of sterility. The affected products were distributed in Pennsylvania.

    Product
    Vancomycin 25mg/mL Solution, 10 mL bottles, Rx only, Walter's Pharmacy 401 N 17th St., Allentown, PA 610-435-4706, NDC 99999-9003-78
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0798-2016·2016-04-06

    Walter's Pharmacy Recalls Tobramycin Ophthalmic Solution Due to Sterility Concerns

    Walter's Pharmacy is recalling Tobramycin 14 mg/mL Ophthalmic Solution because the product lacks assurance of sterility. The recall affects 10 mL bottles distributed in Pennsylvania.

    Product
    Tobramycin 14 mg/mL Ophth Solution, 10mL bottle, Rx only, Walter's Pharmacy, 401 N 17th St, Allentown, PA 610-435-4706, NDC 99999-9996-60
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0782-2016·2016-04-06

    Praxair Recalls 127 Cylinders of Compressed Medical Air Due to Odor

    Praxair Inc. is recalling 127 cylinders of compressed medical air because a customer reported an odor when turning on a cylinder.

    Product
    UN1002 Air, Compressed, Breathing Grade, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113, NDC 59579-006.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0785-2016·2016-04-06

    Safecor Health Recalls Donnatal Elixir Due to Labeling Error

    Safecor Health is recalling 23 cups of Donnatal Elixir because the label incorrectly lists the dose as 5 ml instead of 10 ml.

    Product
    Phenobarbital/Hyoscyamine/ Atropine/Scopolamine 16.2/0.1037/0.0194/0.0065 mg DONNATAL ELIXIR, 5 ml Cup grape, Alcohol 23.8%, Rx Only, MFG: Concordia, PKG BY: SAFECOR HEALTH, WOBURN, MA, C5921242304.
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Drugs)·D-0783-2016·2016-04-06

    Praxair Recalls Medical Air Cylinders Due to Odor Complaint

    Praxair Inc. is recalling 382 cylinders of medical air nationwide after a customer reported an odor when turning on a cylinder.

    Product
    UN1002 Air, Compressed, Medical Air, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113,
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0800-2016·2016-04-06

    Pfizer Recalls Robitussin Peak Cold Liquid Due to Labeling Error

    Pfizer is recalling 63,636 bottles of Robitussin Peak Cold Liquid nationwide due to a label mix-up. Consumers should stop using the product and return it to the point of purchase.

    Product
    Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle (237 mL), Distributed by Pfizer, Madison, NJ 07940, NDC 0031-8736-18
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0780-2016·2016-03-30

    Sagent Recalls Fluconazole Injection Due to Cross-Contamination with Metronidazole

    Sagent Pharmaceuticals is recalling specific lots of Fluconazole Injection due to cross-contamination with metronidazole. The affected product is distributed nationwide and in Puerto Rico.

    Product
    Fluconazole Injection, USP (in 0.9% Sodium Chloride), 200 mg per 100 ml, Single-Dose Container Bag, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195, NDC 25021-0113-82
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0779-2016·2016-03-30

    AGA Gas Recalls Bulk Liquid Oxygen Due to GMP Deviations

    AGA Gas Inc is recalling 1,500 gallons of bulk liquid oxygen because the delivery trailer may not have met GMP requirements prior to filling.

    Product
    Oxygen, USP, 99.0%, Bulk Cryogenic Liquid, Rx, Airgas Merchant Gases, LLC, Independence, OH --- NDC 33237-001-01
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0781-2016·2016-03-30

    AstraZeneca Recalls Tudorza Pressair Inhalers Due to Defective Delivery System

    AstraZeneca is recalling Tudorza Pressair inhalers because some units have actuation counters set to a number other than 60.

    Product
    Tudorza Pressair (aclindinium bromide inhalation powder), 400 mcg per actuation, 60 Metered Doses per Inhaler, Rx Only. Manufactured for: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850. Manufactured by: Forest Laboratories, Ireland Limited, Dublin 17 Ireland. Product of…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0774-2016·2016-03-23

    Teva Recalls Paricalcitol Capsules Due to Impurity Test Failures

    Teva Pharmaceuticals is recalling Paricalcitol Capsules because stability testing revealed out-of-specification impurities. The recall covers 30,891 bottles distributed nationwide and in Puerto Rico.

    Product
    Paricalcitol Capsules, 1 mcg, 30 tablets per Bottle, Rx Only, Manufactured By: Pharmaceutics International, Inc., Hunt Valley, MD 21031, Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-7656-56.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0777-2016·2016-03-23

    Pharmedium Recalls Subpotent Epinephrine Injection Bags

    Pharmedium Services, LLC is recalling 6,816 bags of subpotent epinephrine injection due to discoloration and FDA-confirmed potency issues.

    Product
    NORepinephrine Bitartrate, 4 mg (16 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag, Rx only, PharMEDium Services, LLC, Sugar Land, TX NDC 61553-134-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0776-2016·2016-03-23

    Medical Park Homecare Recalls Compressed Oxygen Cylinders Due to Gauge Issues

    Medical Park Homecare is recalling compressed oxygen cylinders filled using out-of-date gauges. The recall involves M6, D, and E tanks distributed in Oklahoma.

    Product
    Oxygen, Compressed USP (Gaseous, Medical Oxygen, Aluminum Cylinders), Packaged in a) M6-Tanks, b) D-Tanks, and c) E-Tanks, Rx Only. Medical Park Homecare, 139 SE Katherine Ave., Bartlesville, OK 74006.
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Drugs)·D-0773-2016·2016-03-23

    Teva Recalls Nabumetone Tablets Due to Missing Labels and Leaflets

    Teva Pharmaceuticals USA is recalling 576 bottles of Nabumetone 750 mg tablets because they lack required leaflets and approved labels.

    Product
    NABUMETONE Tablets USP, 750 mg, 100 count bottle,Teva Pharmaceutical Industries Ltd., Jerusalem, 91010, ISRAEL
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0778-2016·2016-03-23

    Pharmedium Recalls Subpotent Repinephrine Bitartrate Injection Bags

    Pharmedium Services, LLC is recalling specific lots of repinephrine bitartrate injection bags due to subpotency and discoloration confirmed by FDA analysis.

    Product
    NORepinephrine Bitartrate, 8 mg (32 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag Black, Rx only, PharMEDium Services, LLC, Sugar Land, TX NDC 61553-127-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0775-2016·2016-03-23

    Virt-Nate Prenatal Supplement Recalled for Incorrect Tablet Imprinting

    Virtus Pharmaceuticals is recalling Virt-Nate Prenatal/Postnatal supplements because some bottles contain tablets with the wrong identification code.

    Product
    Virt-Nate Prenatal/Postnatal, Prescription Folate-Containing Dietary Supplement, Rx, 100 count bottles, Manufactured For: Virtus Pharmaceuticals, Tampa, FL
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0771-2016·2016-03-16

    Tf Supplements Recalls Rhino 7 3000 Due to Undeclared Ingredients

    Tf Supplements is recalling Rhino 7 3000 bottles because they contain undeclared desmethyl carbondenafil and dapoxetine and were marketed without an approved NDA or ANDA.

    Product
    RHINO 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0772-2016·2016-03-16

    Rhino 7 Platinum 3000 Recalled for Undeclared Active Ingredients

    Tf Supplements is recalling Rhino 7 Platinum 3000 because it contains undeclared desmethyl carbondenafil and dapoxetine and was marketed without an approved NDA or ANDA.

    Product
    Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA, UPC 700729253748
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0749-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Hydromorphone and Bupivacaine Syringes

    Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.

    Product
    Hydromorphone HCL 20 mg/ml/Bupivacaine HCL 40 mg/ml, vol. 20 ml syringe Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide