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:
Batch No. | Description | Expiry |
---|---|---|
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.
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