We wish to advise you that all in-date batches of Kexxtone 32.4g continuous-release intraruminal device for cattle are being recalled with immediate effect.
This recall is going to Veterinarian / Pharmacy level.
The reason for the recall is due to a quality defect which has resulted in cases where cattle regurgitated the device while it still contained monensin tablets. This resulted in increased accidental exposure, including deaths, in non-target species (dogs) and potential lack of efficacy in cattle.
The attached recall letters and Direct animal Healthcare Professional Communication (DaHPC) provide additional information in relation to this issue:
Veterinarian / Pharmacist Recall Letter
Wholesaler Recall Letter
Direct animal Healthcare Professional Communication (DaHPC)
A Safety Warning has previously been issued for this medicine.
Actions To Be Taken:
Information for veterinarians / pharmacists:
Please immediately perform the following actions:
- Quarantine any in-date units of this product which you have in your possession.
- For pharmacists only, please check your dispensing records and identify prescribers of the product and forward them a copy of the DaHPC.
- If you have supplied any other veterinarian, pharmacy, clinic or other such establishment with units of this product, please provide them with a copy of the recall letter and DaHPC, and request they quarantine and return unsold stock to you.
- Contact the wholesaler from which you purchased the stock to arrange for the return of all quarantined units.
There is no requirement to contact end users of the product, as this is a veterinarian / pharmacy level recall.
Information for end users of the product:
If you are using this product and have any queries, please contact your veterinarian / pharmacist.