The Recall Desk

Hazard

Chemical Contamination recalls

415 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
415
Critical
15
Severe
92
Most recent
2026-09-09

Of the 415 chemical contamination recalls we have scored against our rubric, 15 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 92 (22%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all chemical contamination recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

376–400 of 415

  • ModerateFDA (Drugs)·D-338-2014·2013-12-18

    Novartis Recalls Tekturna Tablets Due to Chemical Contamination

    Novartis is recalling Tekturna physician sample bottles contaminated with Darocur 1173, a photocuring agent found in ink.

    Product
    Tekturna (aliskiren) Tablets 300 mg, 7 tablets per bottle, Physician Sample-Not For Sale, Rx only. Manufactured by: Novartis Pharma Produktions GmbH Wehr, Germany. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC # 0078-9486-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0347-2014·2013-12-04

    Renew Life DigestMORE Food Supplements Recalled for Chloramphenicol Contamination

    Pacific Nutritionals is recalling Renew Life DigestMORE and DigestMORE Ultra food supplements because they are contaminated with Chloramphenicol.

    Product
    -DigestMORE, 90 capsules per bottle, Food Supplement is sold under Renew Life brand. The UPC Code 6 31257 35000 8. -DigestMORE Ultra, 60 capsules per bottle, Food Supplement is sold under Renew Life brand. The UPC Code 6 31257 35001 5. The DigestMORE product is labeled i
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0381-2014·2013-12-04

    Houston Nutraceuticals Recalls TriEnza Bulk Powder for Chloramphenicol

    Houston Nutraceuticals is recalling TriEnza bulk powder because it may contain chloramphenicol above permitted limits. The product was distributed internationally to Brazil.

    Product
    TriEnza bulk powder distributed in a 5 kilogram polyethylene bag.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0095-2014·2013-11-13

    American Laboratories Recalls Ultra Blend 102 Enzyme Powder Due to Contamination

    American Laboratories Inc is recalling Ultra Blend 102 enzyme powder due to potential Chloramphenicol contamination. The product was distributed to five states.

    Product
    Ultra Blend 102, powder, enzyme blend, packaged in 25 kg double poly bags inside fiber box. Product 73B, SI Item # 10678.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-331-2013·2013-05-22

    Glenmark Recalls Topiramate Tablets Due to Off-Odor Complaints

    Glenmark Generics Inc. is recalling Topiramate Tablets due to complaints of a moldy, musty, or fishy odor. The recall covers 9,624 bottles distributed nationwide.

    Product
    TOPIRAMATE — TOPIRAMATE (TOPIRAMATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1380-2013·2013-05-15

    Winn-Dixie Organic Apple Juice Recalled for Potential Patulin Levels

    Winn-Dixie Logistics is recalling 6,104 bottles of Organic 100% Apple Juice because it may contain patulin levels exceeding FDA limits.

    Product
    Winn Dixie Organic 100% Apple Juice from concentrate with added ingredients, 64-fl oz
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-317-2013·2013-05-15

    Physicians Total Care Recalls Plavix 75 mg Due to Moldy Odor

    Physicians Total Care is recalling specific bottles of Plavix 75 mg tablets due to a chemical contamination causing an uncharacteristic moldy odor.

    Product
    Plavix 75 mg, 30 count bottle, NDC (54868-4070-0), Rx only, Manufactured by Bristol-Meyers Squibb, Bridgewater, NJ 08807, Distributed by Physicians Total Care, Tulsa, OK 74146.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-304-2013·2013-05-08

    Warner Chilcott Recalls Jevantique Tablets Due to Chemical Contamination

    Warner Chilcott is recalling Jevantique tablets because 2-phenylphenol was found in the product. The contamination resulted from migration from the cardboard cartons used for packaging.

    Product
    Jevantique (norethindrone acetate and ethinyl estradiol) tablets; 1.0 mg/5.0 mcg, 90 count bottle (NDC# 52544-237-19), Rx only, Manufactured by Warner Chilcott Company, LLC, Fajardo, PR 00738, Distributed by Watson Pharma, Inc. Corona, CA 92880.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-303-2013·2013-05-08

    Warner Chilcott Recalls Femhrt Tablets Due to Chemical Contamination

    Warner Chilcott is recalling specific lots of Femhrt tablets because 2-phenylphenol was found in the product. The chemical migrated from the cardboard cartons used for packaging.

    Product
    Femhrt (norethindrone acetate and ethinyl estradiol) tablets, 0.5 mg/2.5 mcg, 90 count bottle (NDC#: 0430-0145-23), Rx only, Manufactured by Warner Chilcott Company, LLC, Fajardo, PR 00738, Marketed by Warner Cholcott (US), LLC, Rockaway, NJ 07866
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-305-2013·2013-05-08

    Warner Chilcott Recalls Femhrt Tablets Due to Chemical Contamination

    Warner Chilcott is recalling 6,408 bottles of Femhrt tablets because 2-phenylphenol was found in the product. The chemical migrated from the cardboard cartons used for packaging.

    Product
    Femhrt (norethindrone acetate and ethinyl estradiol) tablets, 1.0 mg/5.0 mcg, 90 count bottle ( NDC#: 0430-0544-23), Rx only, Manufactured by Warner Chilcott Company, LLC, Fajardo, PR 00738, Marketed by Warner Cholcott (US), LLC, Rockaway, NJ 07866
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-251-2013·2013-04-24

    Pfizer Recalls Levoxyl Tablets Due to Chemical Odor

    Pfizer is recalling Levoxyl (levothyroxine sodium) tablets because they emit a strong odor after the package is opened.

    Product
    LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-261-2013·2013-04-24

    Pfizer Recalls Levoxyl Tablets Due to Strong Odor Contamination

    Pfizer is recalling specific lots of Levoxyl tablets because they emit a strong odor after the package is opened.

    Product
    LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-253-2013·2013-04-24

    Pfizer Recalls Levoxyl Tablets Due to Strong Odor Contamination

    Pfizer is recalling Levoxyl (levothyroxine sodium) tablets because they emit a strong odor after the package is opened.

    Product
    LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-257-2013·2013-04-24

    Pfizer Recalls Levoxyl Tablets Due to Strong Odor Contamination

    Pfizer is recalling Levoxyl (levothyroxine sodium) tablets because they emit a strong odor after the package is opened.

    Product
    LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-254-2013·2013-04-24

    Pfizer Recalls Levoxyl Tablets Due to Strong Odor Contamination

    Pfizer is recalling specific lots of Levoxyl tablets because they emit a strong odor after opening. Consumers should stop using the affected products.

    Product
    LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-259-2013·2013-04-24

    Pfizer Recalls Levoxyl Tablets Due to Chemical Odor Contamination

    Pfizer is recalling specific lots of Levoxyl (levothyroxine sodium) tablets because they emit a strong chemical odor after the package is opened.

    Product
    LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-260-2013·2013-04-24

    Pfizer Recalls Levoxyl Tablets Due to Chemical Odor Contamination

    Pfizer is recalling specific lots of Levoxyl tablets because they emit a strong odor after opening. The recall covers 10,121 bottles distributed nationwide and in Puerto Rico.

    Product
    LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-256-2013·2013-04-24

    Pfizer Recalls Levoxyl Tablets Due to Strong Odor Emission

    Pfizer is recalling specific lots of Levoxyl tablets because they emit a strong odor after the package is opened.

    Product
    LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-252-2013·2013-04-24

    Pfizer Recalls Levoxyl Tablets Due to Chemical Odor Contamination

    Pfizer is recalling Levoxyl (levothyroxine sodium) tablets because they emit a strong odor after the package is opened.

    Product
    LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-255-2013·2013-04-24

    Pfizer Recalls Levoxyl Tablets Due to Chemical Odor Contamination

    Pfizer is recalling specific lots of Levoxyl tablets because they emit a strong chemical odor after the package is opened.

    Product
    LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1286-2013·2013-04-10

    Beehive Botanicals Recalls Propolis Powder Due to Fluvalinate Contamination

    Beehive Botanicals, Inc. is recalling specific lots of Propolis Powder because they tested positive for Fluvalinate.

    Product
    Propolis Powder -100% Standardized Bee-Propolis Lot #: 021113-55/60, EXP: 10/14 11# Bag & Lot#: 10081155/60-120612-100, EXP: 12/15, 1# BAG.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-1244-2013·2013-03-27

    Wynlife Recalls Probiotics and Vegi-Fiber Plus Due to DEHP Contamination

    Wynlife Healthcare is recalling All-In-One Probiotics and Vegi-Fiber Plus products because they contain DEHP-contaminated clouding agents.

    Product
    All-In-One Probiotics, K12-BB12-LB3; Dietary Supplement; 30 Packets;Serving size 2 Tablets (1 Packet)l L141/1. Adults take 2 to 4 tablets daily; Children: take 1 to 2 tablets daily (or as directed by your healthcare practitioner. Chew slowly or allow to dissolve in mouth. Manufac
    Category
    Food
    Distribution
    Distributed nationwide