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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

Various Akorn Veterinary Medications Recalled for Quality and Stability Concerns

Agency Publication Date: June 15, 2023
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Summary

Akorn, Inc. is recalling approximately 842,949 units of various veterinary medications, including Artificial Tears, Atropine Sulfate, and Ketamine injections, because the company has gone out of business and can no longer guarantee the quality or stability of the products through their expiration dates. This recall affects a wide range of sterile ophthalmic ointments, solutions, and injectable medications used for pets and horses. The products were distributed nationwide to veterinary clinics, pharmacies, and through MWI Animal Health.

Risk

The medications may lose their effectiveness or become unstable over time, which could lead to treatment failure or potential safety issues for animals receiving the drugs. No injuries or adverse events have been reported to date.

What You Should Do

  1. Identify if you have any of the affected products by checking for the brands Artificial Tears, Atropine Sulfate Ophthalmic Solution, Butorphanol tartrate, Butorphic, Ketamine HCl, Neomycin/Polymyxin B/Bacitracin Zinc ointment, Proparacaine Hydrochloride, Tobramycin Ophthalmic Solution, VetaKet, or Vetorphic.
  2. Check your packaging for the product name and NDC (National Drug Code); this recall affects ALL lots and ALL NDCs for the listed products. See the Affected Products section below for the full list of affected codes.
  3. If you have animal health concerns, contact your veterinarian. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer or supplier for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 if you have additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: If you have animal health concerns, contact your veterinarian. Return any unused product to the place of purchase for a refund, or contact the manufacturer or supplier for further instructions.
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Artificial Tears Lubricant ophthalmic ointment (3.5 g)
Variants: Sterile, Ointment
Lot Numbers:
ALL LOTS
NDC:
ALL NDCs

Recall #: V-0129-2023; Quantity: 576,032 tubes

Product: Atropine Sulfate Ophthalmic Solution, USP 1% (5 mL)
Variants: Sterile, Solution
Lot Numbers:
ALL LOTS
NDC:
ALL NDCs

Recall #: V-0130-2023; Distributed by MWI; Quantity: 9,515 bottles

Product: Butorphanol tartrate injection (20 or 50 mL)
Variants: Injection
Lot Numbers:
ALL LOTS
NDC:
ALL NDCs

Recall #: V-0131-2023; For use in horses only; Quantity: 28,547 vials

Product: Butorphic (Butorphanol tartrate injection) (20 or 50 mL)
Variants: Injection
Lot Numbers:
ALL LOTS
NDC:
ALL NDCs

Recall #: V-0132-2023; For use in horses only; Quantity: 11,221 vials

Product: Ketamine HCl injection, USP (10 mL)
Variants: Injection
Lot Numbers:
ALL LOTS
NDC:
ALL NDCs

Recall #: V-0133-2023; Quantity: 3,408 vials

Product: Neomycin and Polymyxin B Sulfates, and Bacitracin Zinc Ophthalmic Ointment, USP (3.5 g)
Variants: Ointment
Lot Numbers:
ALL LOTS
NDC:
ALL NDCs

Recall #: V-0134-2023; Quantity: 121,356 tubes

Product: Proparacaine Hydrochloride Ophthalmic Solution USP, 0.5% (15 mL)
Variants: Solution, Topical
Lot Numbers:
ALL LOTS
NDC:
ALL NDCs

Recall #: V-0135-2023; Quantity: 960 bottles

Product: Tobramycin Ophthalmic Solution, USP 0.3% (5 mL)
Variants: Solution
Lot Numbers:
ALL LOTS
NDC:
ALL NDCs

Recall #: V-0136-2023; Quantity: 56,904 bottles

Product: VetaKet (Ketamine HCl Injection, USP) (10 mL)
Variants: Injection
Lot Numbers:
ALL LOTS
NDC:
ALL NDCs

Recall #: V-0137-2023; Quantity: 5,324 vials

Product: Vetorphic (butorphanol tartrate injection) (20 mL)
Variants: Injection, 10 mg/mL
Lot Numbers:
ALL LOTS
NDC:
ALL NDCs

Recall #: V-0138-2023; Quantity: 29,682 vials

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92478
Status: Active
Manufacturer: Akorn, Inc.
Sold By: MWI; veterinary clinics; pharmacies
Manufactured In: United States
Units Affected: 10 products (576,032 tubes; 9,515 bottles; 28,547 vials; 11,221 vials; 3,408 vials; 121,356; 960 bottles; 56,904 bottles; 5,324 vials; 29,682 vials)
Distributed To: Nationwide
Agency Last Updated: July 3, 2023

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 FDA Press Release ยท Raw API Response