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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Vet
Pets & Animals/Pet Medications

Safe-Guard Medicated Dewormer for Beef Cattle Recalled for Labeling Errors

Agency Publication Date: August 9, 2021
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Summary

Intervet, Inc. is voluntarily recalling 20,192 blocks of Intervet Safe-Guard (fenbendazole) Medicated Dewormer for Beef Cattle 20% Protein Block. The recall was initiated because several ingredients listed on the label (magnesium oxide, calcium phosphate, monocalcium phosphate, and hemicellulose extract) are no longer in the product's formulation or have been replaced by other binders like lignin sulfonate. This results in inaccurate product labeling for livestock owners.

Risk

The product formulation does not match the printed label, which could lead to incorrect nutritional management of beef cattle, though no incidents or injuries have been reported to date.

What You Should Do

  1. Check your product packaging for the UPC code 021784464253 and specific lot codes and manufacture dates, such as D9194001 (13Jul21) or D1014002 (14Jan23). See the Affected Products section below for the full list of affected codes.
  2. Stop using the recalled product. Contact the manufacturer or your distributor to arrange return or proper disposal.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 if you have further questions or need to report an issue.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return or proper disposal.

Affected Products

Product: Intervet Safe-Guard (fenbendazole) Medicated Dewormer for Beef Cattle 20% Protein Block (25 LBS)by Safe-Guard
UPC Codes:
021784464253
Lot Numbers:
D9194001 (13Jul21)
D0106001 (15Apr22)
D9198002 (17Jul21)
D0113002 (22Apr22)
D9199003 (18Jul21)
D0125001 (04May22)
D9214001 (02Aug21)
D0132002 (11May22)
D9220002 (08Aug21)
D0171001 (19Jun22)
D9224003 (12Aug21)
D0177002 (25Jun22)
D9234004 (22Aug21)
D0203001 (21Jul22)
D9259001 (16Sep21)
D0227001 (14Aug22)
D9277001 (04Oct21)
D0231002 (18Aug22)
D9281002 (08Oct21)
D0248001 (04Sep22)
D9301005 (28Oct21)
D0255002 (11Sep22)
D9301004 (28Oct21)
D0269003 (25Sep22)
D9301003 (28Oct21)
D0287001 (13Oct22)
D9304006 (31Oct21)
D0308001 (03Nov22)
D9326001 (22Nov21)
D0310002 (05Nov22)
D9343001 (09Dec21)
D0323003 (18Nov22)
D9365002 (31Dec21)
D0335004 (30Nov22)
D0058001 (27Feb22)
D0352001 (17Dec22)
D0059002 (28Feb22)
D0358002 (23Dec22)
D0062001 (02Mar22)
D0365003 (30Dec22)
D0070002 (10Mar22)
D1013001 (13Jan23)
D0071003 (11Mar22)
D1014002 (14Jan23)
D0085004 (25Mar22)

Recall #: V-0147-2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 88368
Status: Resolved
Manufacturer: Intervet, Inc
Sold By: Sweetlix; Intervet Inc.
Manufactured In: United States
Units Affected: 20,192 blocks
Distributed To: Tennessee, Colorado, Ohio, Missouri, Arkansas, Idaho, Texas, Wyoming, Alabama
Agency Last Updated: August 19, 2021

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response