Baxter — Class II medical device recall Z-0731-2016
Terminated recall by Baxter Corporation Englewood, reported 2016-02-10, distributed nationwide. All lots of RAPIDFILL Syringe Strips lack evidence supporting the packaging claim for 12-month shelf life on r
| Recall number | Z-0731-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Corporation Englewood, Englewood, CO, United States |
| Recall initiated | 2015-12-21 |
| Classified | 2016-01-30 |
| Reported by FDA | 2016-02-10 |
| Terminated | 2016-08-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, DE, NL, SE |
| Quantity | 4,695 |
Product
Baxter, RAPIDFILL Syringe Strip, 10 ml. For use with RAPIDFILL Automated Syringe Filler (ASF)
Reason for recall
All lots of RAPIDFILL Syringe Strips lack evidence supporting the packaging claim for 12-month shelf life on released product.
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/Z-0731-2016. 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.