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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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Medium RiskFDA Vet
Pets & Animals/Pet Medications

XF Enterprises, Inc: SHOWMAXX and SHOWFLEXX Cattle Feed Recalled for Missing Labels

Agency Publication Date: June 4, 2012
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Summary

XF Enterprises, Inc. is recalling approximately 7,373 buckets of SHOWMAXX Zilmax and SHOWFLEXX medicated cattle feed supplements. These products are missing required safety labeling, and the SHOWMAXX variety was produced at an unlicensed feed mill. The affected products were sold in 10-lb and 15-lb buckets across Texas and Iowa. Because these products contain medicated ingredients like zipaterol hydrochloride and ractopamine hydrochloride, they must be used according to specific label instructions to ensure animal safety and proper food production standards.

Risk

The lack of required labeling means that users may not have critical instructions for the safe administration of medicated feed, which could lead to improper dosing or residues in livestock. Furthermore, the SHOWMAXX product was manufactured at an unlicensed facility, meaning it was produced without the regulatory oversight required to ensure quality and safety standards.

What You Should Do

  1. Check your supplies for SHOWMAXX Zilmax (zipaterol hydrochloride 4.8%) in 10-lb buckets (Recall #: V-075-2012) or SHOWFLEXX Medicated with Optaflexx in 15-lb buckets (Recall #: V-076-2012).
  2. Immediately stop using these feed supplements for your livestock to avoid potential dosing errors or regulatory non-compliance.
  3. Contact your veterinarian or animal health consultant for guidance on alternative feeding programs and to discuss any concerns regarding animals that have already consumed the product.
  4. Return any unused buckets to the place of purchase (such as Sullivan Supply South, Inc. in Texas or Sullivan Supply, Inc. in Iowa) for a full refund.
  5. Contact X.F. Enterprises, Inc. at their Hereford, Texas office or reach out to the distributing retailers for further instructions on returning the product.
  6. For additional questions, contact the FDA Center for Veterinary Medicine at 240-402-7002.

Your Remedy Options

๐Ÿ’ฐFull Refund

Return to place of purchase for refund.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: SHOWMAXX Zilmax (zipaterol hydrochloride 4.8%) (10 lbs.)
Model:
V-075-2012
Product: SHOWFLEXX MEDICATED With Optaflexx (15 lb)
Model:
V-076-2012

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 61438
Status: Resolved
Manufacturer: XF Enterprises, Inc
Sold By: Sullivan Supply South, Inc.; Sullivan Supply, Inc.
Manufactured In: United States
Units Affected: 2 products (6368 buckets; 1005 buckets)
Distributed To: Texas, Iowa

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

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