DMSO 50% 60 mL/Heparin 1 mL/ Sodium Bicarbonate 60 mL/ Solu-Cortef… — Class II drug recall D-1142-2019
Terminated recall by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy, reported 2019-04-24, distributed nationwide. Lack of sterility assurance.
| Recall number | D-1142-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy, Bristol, TN, United States |
| Recall initiated | 2019-04-02 |
| Classified | 2019-04-18 |
| Reported by FDA | 2019-04-24 |
| Terminated | 2021-09-24 |
| Distributed | Nationwide (US) |
| Quantity | 1 syringes |
| Reason classes | sterility |
Product
DMSO 50% 60 mL/Heparin 1 mL/ Sodium Bicarbonate 60 mL/ Solu-Cortef 100 mg, 41 mL syringe, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.
Reason for recall
Lack of sterility assurance.
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-1142-2019. 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.