Liver Derivative Complex for injection — Class II drug recall D-1389-2014
Terminated recall by John W Hollis Inc, reported 2014-06-25, distributed nationwide. Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable produc
| Recall number | D-1389-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | John W Hollis Inc, Nashville, TN, United States |
| Recall initiated | 2014-05-12 |
| Classified | 2014-06-18 |
| Reported by FDA | 2014-06-25 |
| Terminated | 2014-07-02 |
| Distributed | Nationwide (US) |
| Quantity | 1,560 ml |
| Reason classes | sterility |
| Lot numbers | 1370, 1818, 2664, 938 |
| Expiration dates | 2014-08-17, 2014-11-08, 2015-04-18 |
Product
Liver Derivative Complex for injection, each mL contains: Liver Derivative Complex 25.5mg, also contains: Water for Injection, Phenol 0.5%, HCl or NaOH to adjust pH, 10 mL, Compounded by Prescription: JOHN HOLLIS Pharmacist Inc, 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
Reason for recall
Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
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-1389-2014. 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.