FDA recall, , Moderate risk
Covetrus and VetOne Amoxicillin and Clavulanate Potassium Oral Suspension Drops for Dogs and Cats
This voluntary recall is due to market complaints pertaining to product discoloration following reconstitution.
Summary by Recall Canary from the FDA notice
What happened
Cronus Pharma voluntarily recalled covetrus Amoxicillin and Clavulanate Potassium for Oral Suspension Drops, 62.5mg/mL, 15 mL, and VETONE Betacilin Clav Drops, Amoxicillin and Clavulanate Potassium for Oral Suspension Drops, 15 mL, due to market complaints pertaining to product discoloration following reconstitution. The products, distributed nationwide for use in dogs and cats, were made in India and distributed by Covetrus Noth America and MWI.
2 photos
What to do
We don't have product-specific instructions for this recall. FDA's general advice for recalled products:
- Check the brand, package size and codes such as expiration dates against the notice.
- Return it to the store where you bought it, or dispose of it properly.
Is yours affected?
2 products
Match the lot code and NDC listed under your product.
An NDC (National Drug Code) is usually printed on the drug's label.
VetOne, Betacilin Clav Drops, Amoxicillin and Clavulanate Potassium for Oral Suspension Drops, 15 mL, For use in dogs and cats
- NDC
- 86136-011-15
- Lot code
- FZ6224018A
covetrus, Amoxicillin and Clavulanate Potassium for Oral Suspension Drops
- Strength
- 62.5 mg/mL
- NDC
- 11695-7007-1
- Lot code
- FZ6224017A
Recall details
- Company began the recall
- Sold in
US Nationwide.
- Company
- Cronus Pharma
- Hazard
- Quality problem
- Risk
Moderate risk
It may cause short-term health problems in animals it is used on, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98847
- Recall numbers
- V-0123-2026 to V-0124-2026
All recalls from Cronus Pharma
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report
Listed on Recall Canary
In FDA's weekly enforcement report
Classified by FDA
Summary updated
