Medi-bolic Booster Injectable — Class II drug recall D-191-2013
Terminated recall by RX South LLC DBA RX3 Pharmacy, reported 2013-03-20, distributed nationwide. CGMP Deviations: Pharmaceutical for injection was not manufactured according to Good Manufacturing Procedures.
| Recall number | D-191-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | RX South LLC DBA RX3 Pharmacy, Chester, VA, United States |
| Recall initiated | 2013-01-22 |
| Classified | 2013-03-08 |
| Reported by FDA | 2013-03-20 |
| Terminated | 2013-03-25 |
| Distributed | Nationwide (US) |
| Quantity | 126 vials |
| Reason classes | cgmp |
| Expiration dates | 2013-01-27, 2013-01-28 |
Product
Medi-bolic Booster Injectable (methionine 8.3 mg/mL, choline chloride 16.6 mg/mL, inositol 16.6 mg/mL, cyanocobalamin USP [Vit B12] 0.33 mg/mL, chromium chloride 2.6 mg/mL), 30 mL multi-dose vials, Rx3 Compounding Pharmacy, 12230 Ironbridge Rd., Suite C, Chester, VA 23831.
Reason for recall
CGMP Deviations: Pharmaceutical for injection was not manufactured according to Good Manufacturing Procedures.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-191-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.