FDA Drug recall D-0002-2017
Methylcobalamin 5000 mcg/mL Injection, packaged in 1, 2, 3, 4, and 5 mL vials, IM, Rx, The Apothecary Shoppe Compounding Pharmacy, Jenks, OK
- FDA Drug
- Class II
- terminated
- Published 2016-10-12
On 2016-10-12 the FDA classified a Class II recall of Methylcobalamin 5000 mcg/mL Injection, packaged in 1, 2, 3, 4, and 5 mL vials, IM, Rx, The Apothecary Shoppe Compounding Pharmacy, Jenks, OK by The Apothecary Shoppe, citing lack of Assurance of Sterility; medication was sterilized with a recalled filter.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0002-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-09-12 |
| Published | 2016-10-12 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | The Apothecary Shoppe |
| Distribution | OK |
Product
Methylcobalamin 5000 mcg/mL Injection, packaged in 1, 2, 3, 4, and 5 mL vials, IM, Rx, The Apothecary Shoppe Compounding Pharmacy, Jenks, OK
Reason
Lack of Assurance of Sterility; medication was sterilized with a recalled filter
Identifiers
| code_info | 071222016@24 BUD 01/08/2017, 05112016@8 BUD 11/07/2016 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0002-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.