Phytonadione — Class II drug recall D-0541-2016
Terminated recall by Walgreens Infusion Services, reported 2016-01-06, distributed in TX. Lack of Assurance of Sterility
| Recall number | D-0541-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Walgreens Infusion Services, San Antonio, TX, United States |
| Recall initiated | 2015-11-10 |
| Classified | 2015-12-30 |
| Reported by FDA | 2016-01-06 |
| Terminated | 2017-10-18 |
| Distributed | TX |
| Quantity | 20 syringes |
| Reason classes | sterility |
Product
Phytonadione (Vitamin K) 1 mg/0.1mL Syringe, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Reason for recall
Lack of Assurance of Sterility
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-0541-2016. 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.