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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126–150 of 164

  • SevereFDA (Food)·F-1577-2017·2017-03-22

    Dietary Supplement Recalled for Presence of Banned Ephedra Alkaloid

    Kingsway Trading Inc is recalling Xanthium & Siler Combo (Bi Yan Pian) dietary supplements because they contain Ephedrae Herba (ma huang), a banned ephedra alkaloid.

    Product
    Xanthium & Siler Combo (Bi Yan Pian) DIETARY SUPPLEMENT, Net cont: 100 tablets (300mg each), Net Wt. 1.06oz (30g)
    Category
    Drug
    Distribution
    17 states
  • LowFDA (Food)·F-0820-2017·2016-12-28

    Hi-Tech Pharmacal Recalls Liquid Vitamin C Due to Low Active Ingredient

    Hi-Tech Pharmacal is recalling Rx CHOICE brand Liquid Vitamin C because the active ingredient is at a lower level than stated on the label.

    Product
    Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY 11701
    Category
    Drug
    Distribution
    13 states
  • LowFDA (Food)·F-0817-2017·2016-12-28

    Hi-Tech Pharmacal Recalls Liquid Vitamin C Due to pH Issues

    Hi-Tech Pharmacal is recalling Rx CHOICE brand Liquid Vitamin C because the product failed to meet pH specifications.

    Product
    Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY 11701
    Category
    Drug
    Distribution
    16 states
  • LowFDA (Food)·F-0606-2017·2016-12-14

    Safecor Vitamin B-1 Tablets Recalled for Incorrect Ingredient Labeling

    Safecor Health is recalling Vitamin B-1 tablets because the boxes are labeled with the wrong chemical form of thiamine.

    Product
    Safecor Vitamin B-1 (THIAMINE) 100 mg tablets NDC: 48433-0108-01 Distributed by: SAFECOR HEALTH, 317 NEW BOSTON STREET, WOBURN, MA
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0419-2017·2016-11-16

    Monocal Calcium and Fluoride Supplement Recalled for Excess Fluoride

    Mericon Industries is recalling Monocal Calcium & Fluoride Supplement because it contains an excess amount of fluoride.

    Product
    Monocal, Calcium & Fluoride Supplement, 100 Tablets; Mericon Industries, Inc., Peoria, Illinois 61615; UPC: 0394-0105-02
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Food)·F-0271-2017·2016-11-02

    Pharmatech Recalls Pedia Tri-Vite Drops Due to Potential Contamination

    Pharmatech LLC is recalling 8,712 bottles of Pedia Tri-Vite Drops due to a potential risk of contamination with Burkholderia cepacia.

    Product
    Pedia Tri-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Food)·F-0190-2017·2016-10-26

    Adwe Prenatal Vitamin Recalled for Folic Acid Potency Concerns

    DNE Nutraceuticals Inc. is recalling Adwe Prenatal tablets due to a concern regarding the potency of folic acid. The recall affects 1,200 bottles distributed in New York.

    Product
    Adwe Naturals Prenatal Vitamin Manufactured for: Adwe Laboratories 1274 49 Street Brooklyn, NY 11219 UPC 040168805079
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·F-2071-2016·2016-09-14

    Nature Made Super B-Complex Recalled for Possible Bacterial Contamination

    Pharmavite is recalling Nature Made Super B-Complex vitamins due to possible Staphylococcus aureus and Salmonella contamination in specific lots.

    Product
    Nature Made(R) Super B-Complex, KEY B VITAMINS + VITAMIN C, 460 count, UPC 0-31604-02728-5
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2067-2016·2016-09-14

    Nature Made Multi + Omega-3 Recalled for Possible Salmonella Contamination

    Pharmavite is recalling specific lots of Nature Made Multi + Omega-3 supplements due to possible Salmonella contamination. Consumers should stop using the affected products.

    Product
    Nature Made(R) Multi + Omega-3, 150 count, UPC 0-31604-04173-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2072-2016·2016-09-14

    Nature Made Super B-Complex Recalled for Possible Bacterial Contamination

    Pharmavite is recalling Nature Made Super B-Complex supplements due to possible Staphylococcus aureus and Salmonella contamination in specific lots.

    Product
    Nature Made (R) Super B-Complex, KEY B VITAMINS + VITAMIN C, 360 count, UPC 0-31604-02729-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2078-2016·2016-09-14

    Nature Made Vitamin D Tablets Recalled for Yeast and Mold

    Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.

    Product
    Nature Made(R) D3 1000IU, 350 count, UPC 0-31604-04070-3
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2075-2016·2016-09-14

    Nature Made Vitamin D tablets recalled for yeast and mold

    Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.

    Product
    Nature Made(R) D3 1000IU, 100 count, UPC 0-31604-01870-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2076-2016·2016-09-14

    Nature Made Vitamin D Tablets Recalled for Potential Yeast and Mold

    Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.

    Product
    Nature Made(R) D3 1000IU, 300 count, UPC 0-31604-02683-7
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1163-2016·2016-05-11

    Iowa Select Herbs Recalls Cold Be Gone for Misbranding and Adulteration

    Iowa Select Herbs LLC is recalling Cold Be Gone products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.

    Product
    Iowa Select Herbs LLC, Cold Be Gone, www.iowaselectherbs.com, (a) 1/2 fl. Oz., (b) 15 ml, (c) 1 fl. Oz., (d) 30 ml (e) unknown size, Cedar Rapids, IA 52402
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2956-2015·2015-08-19

    FDA Recalls Maxam Products for Unapproved Drug Claims

    James G. Cole, Inc. is recalling all Maxam brand products nationwide because they are misbranded, adulterated, and unapproved new drugs.

    Product
    ALL MAXAM PRODUCTS: The Maxam product is used orally in spray form and bears the Maxam label. ********The List of MAXAM products********************************************** AD Nutritional Support for a Positive Outlook; AFX Nutritional Support for Healthy Cellular
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2957-2015·2015-08-19

    ASN Dietary Supplements Recalled for Unapproved Drug Claims

    James G. Cole, Inc. is recalling all ASN brand products nationwide because they are misbranded, adulterated, and unapproved new drugs.

    Product
    ALL ASN products: The ASN products are in capsule or powdered form and bear the ASN label. *********the List of ASN products***************************** AFINITY WHEY PROTEIN; DHEA; HUMAGRO Homeopathic Growth Hormone 4c; PHYTOBOL; TESTRX; TRIBESTRONE II;
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2953-2015·2015-08-19

    Chemi-source Recalls DHEA 25mg Capsules for Labeling Inaccuracy

    Chemi-source, Inc. is recalling DHEA 25mg capsules because they may contain more DHEA than the label claims.

    Product
    DHEA 25mg, 60 count, sku: #6-09492-41001-6, and 90 count, sku: #6-09492-41002-3; 12 bottles/case.
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Food)·F-2405-2015·2015-06-17

    Rugby Poly Vitamin Liquid Recalled for Packaging Label Mismatch

    Pharmatech LLC is recalling Rugby Poly Vitamin Liquid, 50ml, because the outside packaging may have incorrect lot, expiration, or product identity information.

    Product
    Rugby Poly Vitamin Liquid, 50ml
    Category
    Drug
    Distribution
    37 states
  • ModerateFDA (Food)·F-2406-2015·2015-06-17

    Rugby Poly Vitamin Liquid Recalled for Packaging Label Mismatch

    Pharmatech LLC is recalling Rugby Poly Vitamin Liquid with Iron because the outside packaging labels may not match the individual product labeling, potentially displaying incorrect lot, expiration, or product identity information.

    Product
    Rugby Poly Vitamin Liquid with Iron, 50 ml
    Category
    Drug
    Distribution
    37 states
  • LowFDA (Food)·F-2323-2015·2015-06-03

    Ubervita Recalls W700 Lose Weight Supplement Due to Packaging Error

    Ubervita LLC is recalling less than 30 units of W700 Lose Weight Fast W700 Thermogenic Hyper-Metabolizer dietary supplements sold at Walmart due to a packaging error.

    Product
    UBERVITA LOSE WEIGHT FAST W700 THERMOGENIC HYPER-METABOLIZER DIETARY SUPPLEMENT. The product has an outer box which contains a labeled bottle. This is a bright red box with gold and chrome foil. Bottle inside is black and red in color. UPC 7 00115 35277 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1380-2015·2015-03-11

    Hi-Tech Pharmacal Recalls Ferrous Sulfate Elixir Due to pH Issues

    Hi-Tech Pharmacal is recalling 581 units of Ferrous Sulfate Elixir because stability testing showed out-of-specification pH results.

    Product
    FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059, NDC 50383-778-05 --- HI-TECH PHARMACAL CO, INC. AMITYVILLE, NY 11701
    Category
    Drug
    Distribution
    5 states