Self-Righting Luer Lock Tip Cap — Class II medical device recall Z-0871-2015
Terminated recall by Baxter Corporation Englewood, reported 2014-12-31, distributed in IL, TX, UT. Baxter Corporation initiated a recall of two lots of Self-Righting Luer Lock Tip Caps because they were distri
| Recall number | Z-0871-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Corporation Englewood, Englewood, CO, United States |
| Recall initiated | 2014-12-04 |
| Classified | 2014-12-24 |
| Reported by FDA | 2014-12-31 |
| Terminated | 2016-11-30 |
| Distributed | IL, TX, UT |
| Countries outside the US | AT, CH, DE, ES, NL |
| Quantity | 54,000 |
| Lot numbers | 1001365, 1001380 |
Product
Self-Righting Luer Lock Tip Cap, Green and Self-Righting Luer Slip Tip Cap, Yellow, Baxter Healthcare Corporation, 14445 Grasslands Dr. Englewood, CO 80112 USA. DISCPAC Syringe Tip Caps. RER H93866100 x 1000. Sterile
Reason for recall
Baxter Corporation initiated a recall of two lots of Self-Righting Luer Lock Tip Caps because they were distributed prior to closure of the validation.
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-0871-2015. 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.