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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

Cydectin (moxidectin) Injection Recalled for Out-of-Specification Alcohol

Agency Publication Date: November 3, 2021
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Summary

Elanco US Inc. is recalling six vials of Cydectin (moxidectin) Injection (10 mg/mL), 500 mL sterile glass vials, because they were formulated with dehydrated alcohol that did not meet UV absorption specifications. This voluntary recall affects a very small number of units (6 vials) distributed in Iowa. Owners should check their vials for Batch SH10127 to see if they are affected.

Risk

The use of out-of-specification alcohol could potentially affect the purity or quality of the injectable medication, though no incidents or injuries have been reported to date.

What You Should Do

  1. Check your product for Cydectin (10 mg moxidectin/mL) in 500 mL glass vials with Batch SH10127 or Lot SH10127.
  2. If you have animal health concerns, contact your veterinarian.
  3. Stop using the recalled product. Contact Elanco US Inc. or your distributor to arrange return or proper disposal.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

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: Cydectin (10 mg moxidectin/mL)by Cydectin
Variants: 500 mL glass vial, Sterile
Lot Numbers:
SH10127

NADA 141-220; Batch SH10127; Shawnee, KS 66216

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 88946
Status: Resolved
Manufacturer: ELANCO US INC
Manufactured In: United States
Units Affected: 6 vials
Distributed To: Iowa
Agency Last Updated: November 18, 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