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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
Medications & Supplements/Veterinary Medicines

LincoBac 300 Lincomycin Injection Recalled for High Impurity Levels

Agency Publication Date: February 8, 2021
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Summary

Sparhawk Laboratories Inc is recalling 10,890 bottles of LincoBac 300 (lincomycin) Injection, a 300 mg/mL antibiotic used for swine. The recall was initiated because the product was found to have levels of a specific impurity (Impurity A) that exceeded the allowed safety specifications. No incidents or adverse health effects have been reported in animals receiving this lot. The product was distributed by MWI and sold in 100 mL glass bottles in Missouri and Kansas.

Risk

Impurity levels higher than approved limits can potentially impact the safety and effectiveness of the antibiotic treatment in swine.

What You Should Do

  1. This recall affects LincoBac 300 (lincomycin) Injection, 300 mg/mL, a swine antibiotic sold in 100 mL glass bottles under NDC 13985-577-10.
  2. Check your supply for lot number 200308, which is the only batch affected by this recall.
  3. Stop using the recalled product immediately.
  4. Contact the manufacturer, Sparhawk Laboratories Inc, or your distributor, MWI, to arrange for the return or proper disposal of the affected medication.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 if you have 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: LincoBac 300 (lincomycin) Injection (100 mL)
Variants: 300 mg/mL, Swine Antibiotic
Lot Numbers:
200308
NDC:
13985-577-10

Distributed by MWI, Boise, ID 83705.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87250
Status: Resolved
Manufacturer: Sparhawk Laboratories Inc
Sold By: MWI
Manufactured In: United States
Units Affected: 10,890 bottles
Distributed To: Missouri, Kansas
Agency Last Updated: February 17, 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