Class 4 Medicines Defect Notification: Viatris Products Ltd, Arixtra solution for injection, pre-filled syringes, EL(26)A/04
UKClass 4 Medicines Defect Notification: Viatris Products Ltd, Arixtra solution for injection, pre-filled syringes, EL(26)A/04
Recalling Firm: Viatris Products Ltd
Reason for Recall / Hazard
Viatris has received reports of brown discolouration and blockage in the needle of pre-filled syringes of Arixtra. This quality defect is related to oxidation of the syringe needle....
Product Description & Identification
Viatris has received reports of brown discolouration and blockage in the needle of pre-filled syringes of Arixtra. This quality defect is related to oxidation of the syringe needle.
Affected Products
Class 4 Medicines Defect Notification: Viatris Products Ltd, Arixtra solution for injection, pre-filled syringes, EL(26)A/04
Additional Source Details
| Field | Value |
|---|---|
| Guid | tag:www.gov.uk,2005:/drug-device-alerts/class-4-medicines-defect-notification-viatris-products-ltd-arixtra-solution-for-injection-pre-filled-syringes-el-26-a-slash-04 |
| Link | https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-notification-viatris-products-ltd-arixtra-solution-for-injection-pre-filled-syringes-el-26-a-slash-04 |
| Pub Date | 2026-01-28T11:00:06+00:00 |
| Extracted category | drugs |
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Overview
- Recalling FirmViatris Products Ltd
- Risk LevelMedicines Recall
- DistributionUnited Kingdom
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🚨 SAFETY ALERT: Viatris Products Ltd - Class 4 Medicines Defect Notification: Viatris Products Ltd, Arixtra solution for injection, pre-filled syringes, EL(26)A/04 Check if your household is affected: https://therecallfile.com/recalls/class-4-medicines-defect-notification-viatris-products-ltd-arixtra-sol/UK-MHRA-class-4-medicines-defect-notification-viatris-products-ltd-arixtra-solution-for-injection-pre-filled-syringes-el-26-a-slash-04
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