Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection — Class II drug recall D-1480-2016
Terminated recall by Isomeric Pharmacy Solution, LLC, reported 2016-09-14, distributed nationwide. Lack of Processing Controls: Isomeric Pharmacy Solution, LLC announces a voluntary field action for the Methyl
| Recall number | D-1480-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Isomeric Pharmacy Solution, LLC, Salt Lake City, UT, United States |
| Recall initiated | 2016-06-29 |
| Classified | 2016-09-02 |
| Reported by FDA | 2016-09-14 |
| Terminated | 2016-12-20 |
| Distributed | Nationwide (US) |
| Quantity | 274 multdose |
| Reason classes | sterility |
| Lot numbers | 03045, 03046, 10/16 |
Product
Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection, 10 mL multidose vial, sterile. Rx only. Compounded by Isomeric Pharmacy Solutions, Salt Lake City, UT 84109,
Reason for recall
Lack of Processing Controls: Isomeric Pharmacy Solution, LLC announces a voluntary field action for the Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection because the sterile injectable products were sterilized too long leading to potential difficulty resuspending particles.
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-1480-2016. 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.