Sterile Water for Injection — Class II drug recall D-1177-2017
Terminated recall by Pfizer Inc., reported 2017-10-04, distributed nationwide. Non-Sterility: cracked or chipped glass at the neck of Sterile Water for Injection vials.
| Recall number | D-1177-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pfizer Inc., New York, NY, United States |
| Recall initiated | 2017-09-01 |
| Classified | 2017-09-22 |
| Reported by FDA | 2017-10-04 |
| Terminated | 2020-01-24 |
| Distributed | Nationwide (US) |
| Quantity | 18,725 vials |
| Reason classes | foreign material, sterility, packaging |
| NDC | 50242-0901-24 |
| Lot numbers | 63-075-DK |
| Expiration dates | 2019-02-20 |
Product
Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc., South San Francisco, CA 94080-4990. NDC 50242-901-24
Reason for recall
Non-Sterility: cracked or chipped glass at the neck of Sterile Water for Injection vials.
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-1177-2017. 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.