Lloyd ToxiBan Charcoal-Kaolin Suspension
ToxiBan Charcoal-Kaolin Suspension has microbial levels exceeding specification limits.
Moderate risk
It may cause temporary or medically reversible health problems in animals it is used on. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Lloyd Inc. of Iowa recalled ToxiBan Charcoal-Kaolin Suspension, Net Volume: 240 mL (8.1 fl oz) per bottle, because microbial levels in the oral medication exceeded the specification limits. The product is for use in domestic animals. The company began the recall on May 15, 2026, and the FDA added it to the Enforcement Report on May 22, 2026.
Summary by Recall Canary from the FDA notice.
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?
Match the NDC and lot code listed under your product.
ToxiBan Charcoal-Kaolin Suspension
- NDC
- 11789-105-50
- Lot
- KA12625
- KA28225
- 2028-MAY
Details
- Company began the recall
- Event ID
- 98996
- Company
- Lloyd Inc. of Iowa
- Hazard
- Contamination
- Quantity recalled
- 6,224 bottles
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
