Following a recent Good Manufacturing Practice (GMP) inspection of one of the active pharmaceutical ingredient (API) manufacturers for Synulox LC, a statement of non-compliance with GMP has been issued.
As a precaution, batches of this product containing API that is impacted by this non-compliance statement are being recalled from the market with immediate effect to the end-user (farm) level. This issue impacts the following batches that have been placed on the UK market:
|91939702||Synulox LC x 12 syringes||31/01/2021|
|81950600||Synulox LC x 12 syringes||30/04/2020|
|81958301||Synulox LC x 12 syringes||30/04/2020|
|81962601||Synulox LC x 12 syringes||31/05/2020|
|81966700||Synulox LC x 12 syringes||30/06/2020|
|81968102||Synulox LC x 12 syringes||30/06/2020|
|81968300||Synulox LC x 12 syringes||30/06/2020|
|91927402||Synulox LC x 12 syringes||30/11/2020|
|91938601||Synulox LC x 12 syringes||31/01/2021|
|91938700||Synulox LC x 12 syringes||31/01/2021|
|91954001||Synulox LC x 12 syringes||31/03/2021|
Zoetis UK Ltd is contacting wholesale dealers and veterinary surgeons to examine inventory immediately and quarantine products subject to this recall.