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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

Lloyd Inc. of Iowa: Lloyd Butorphic Injection Recalled for Incorrect Expiration Date

Agency Publication Date: December 5, 2013
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Summary

Lloyd Inc. of Iowa is recalling 4,466 vials of Lloyd Butorphic Injection (butorphanol tartrate), 10 mg/mL, in 20 mL containers. This veterinary medication is being recalled because the product label lists an incorrect expiration date. Using medication past its actual intended shelf life may lead to reduced effectiveness in treating pain or providing sedation for animals.

Risk

The incorrect expiration date on the label may lead users to administer the medication after it has lost its potency or stability. While the risk level is considered low, inaccurate labeling can result in ineffective treatment for animals requiring pain management.

What You Should Do

  1. Identify if you have the affected product by checking the label for 'Lloyd Butorphic Injection, Butorphanol Tartrate, 10 mg/mL' in 20 mL vials.
  2. Check the packaging for Lot numbers LA28410A or LA29810A to confirm if your specific vials are part of this recall.
  3. Contact your veterinarian or pharmacist immediately to determine if the product in your possession is safe for continued use or if it should be replaced.
  4. Return any unused vials from the affected lots to the pharmacy or place of purchase for a refund.
  5. Contact the manufacturer, Lloyd Inc. of Iowa, for further instructions regarding this recall.
  6. For additional questions or to report concerns, contact the FDA Center for Veterinary Medicine at 240-402-7002.

Your Remedy Options

๐Ÿ’ฐFull Refund

Pharmacy refund and professional consultation.

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

Affected Products

Product: Lloyd Butorphic Injection, Butorphanol Tartrate, 10 mg/mL (20 mL)
Model:
ANDA 200-332
Recall #: V-010-2014
Lot Numbers:
LA28410A
LA29810A

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 66460
Status: Resolved
Manufacturer: Lloyd Inc. of Iowa
Manufactured In: United States
Units Affected: 4,466 vials
Distributed To: Alabama, Arizona, California, Colorado, Florida, Georgia, Hawaii, Iowa, Idaho, Indiana, Kansas, Michigan, Minnesota, Missouri, Mississippi, North Carolina, New York, Pennsylvania, Texas, Virginia, Washington, Wisconsin

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