Recall for Synulox Lactating Cow Intramammary Suspension
The Veterinary Medicines Directorate (VMD has issued a product defect recall alert for Synulox Lactating Cow Intramammary Suspension, manufactured by Zoetis UK.
A statement reads: “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."
Zoetis UK Ltd is contacting veterinary surgeons and wholesaler dealers to examine inventory and quarantine products subject to this recall.
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 24 syringes | 30/04/2020 |
81958301 | Synulox LC x 24 syringes | 30/04/2020 |
81962601 | Synulox LC x 24 syringes | 31/05/2020 |
81966700 | Synulox LC x 24 syringes | 30/06/2020 |
81968102 | Synulox LC x 24 syringes | 30/06/2020 |
81968300 | Synulox LC x 24 syringes | 30/06/2020 |
91927402 | Synulox LC x 24 syringes | 30/11/2020 |
91938601 | Synulox LC x 24 syringes | 31/01/2021 |
91938700 | Synulox LC x 24 syringes | 31/01/2021 |
91954001 | Synulox LC x 24 syringes | 31/03/2021 |