Potassium PHOSphate in 5% Dextrose Injection — Class II drug recall D-0989-2017
Terminated recall by PharMedium Services, Llc, reported 2017-07-26, distributed nationwide. Lack of Assurance of Sterility; media fill failure at manufacturer
| Recall number | D-0989-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | PharMedium Services, Llc, Sugar Land, TX, United States |
| Recall initiated | 2017-06-26 |
| Classified | 2017-07-14 |
| Reported by FDA | 2017-07-26 |
| Terminated | 2020-04-29 |
| Distributed | Nationwide (US) |
| Reason classes | sterility |
| NDC | 61553-0283-03 |
| Lot numbers | 171350099S |
Product
Potassium PHOSphate in 5% Dextrose Injection, 30 mMol 500 mL in 500 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5283 NDC# 61553-283-03
Reason for recall
Lack of Assurance of Sterility; media fill failure at manufacturer
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-0989-2017. 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.