Potassium Phosphate — Class II drug recall D-0956-2017
Terminated recall by Advanced Pharma Inc., reported 2017-07-19, distributed nationwide. Lack of Assurance of Sterility
| Recall number | D-0956-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Advanced Pharma Inc., Houston, TX, United States |
| Recall initiated | 2017-06-22 |
| Classified | 2017-07-07 |
| Reported by FDA | 2017-07-19 |
| Terminated | 2017-12-06 |
| Distributed | Nationwide (US) |
| Reason classes | sterility |
| NDC | 15082-0922-25 |
| Lot numbers | 1100, 1415, 1446, 382-92225P, 515-92225P |
| Expiration dates | 2017-08-29, 2017-08-31, 2017-09-05 |
Product
Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 15 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-922-25
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-0956-2017. 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.