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 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 |
Zoetis UK Ltd is contacting wholesale dealers and veterinary surgeons to examine inventory immediately and quarantine products subject to this recall.
For further information regarding the recall, please contact Zoetis on 0845 300 8034
Last updated 20 December 2019 + show all updates
- Correction to Syringe pack sizes
- First published.
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