VECURONIUM BROMIDE Recall D-1079-2022
Description: Vecuronium Bromide for Injection, 10 mg (1mg/ mL) vial, 10-count box, Rx only, MFG: Teva Pharma USA, NDC 0703-2914-03
VECURONIUM BROMIDE Recall D-1079-2022 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | D-1079-2022 |
| Event ID | 89646 |
| Brand | VECURONIUM BROMIDE |
| Generic Name | VECURONIUM BROMIDE |
| Manufacturer | VECURONIUM BROMIDE |
| Original Package? | 1 |
| Active Substance | VECURONIUM BROMIDE |
| Drug Route | INTRAVENOUS |
| Distribution | USA nationwide. |
| Quantity | 20 cartons/10 vials each |
| Recall Reason | cGMP deviations: Temperature abuse |
| Drug Classification | Class II |
| Drug Code Info | 20220615 |
| Product NDC | 0703-2914 0703-2925 |
| Recall Initiation Date | 20220413 |
| Report Date | 20220615 |
| Classification Date | 20220609 |
| Address | 9954 Maryland DriveDeep Run Iii Ste. 4000 Richmond, VA 23233 United States |
| Recalling Firm | Mckesson Medical-Surgical Inc. Corporate Office |
| Initial Notification | Letter |
| Unique Ingredient Identifier | 7E4PHP5N1D |
| Drug Application Number | ANDA074688 |
| Structured Product Labeling (SPL ID) | 7525d8ef-dedb-42b0-85d4-0e596af4aec7 |
| Structured Product Labeling (SPL Set ID) | eaa404d1-68a9-4fac-b3f3-b444a20df120 |
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