Baxter DISCPAC Syringe Tip Caps — Class II medical device recall Z-0948-2022
Terminated recall by Baxter Healthcare Corporation, reported 2022-04-27, distributed nationwide. Product is mislabeled as self-righting Luer slip tip caps, yellow.
| Recall number | Z-0948-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2022-02-25 |
| Classified | 2022-04-15 |
| Reported by FDA | 2022-04-27 |
| Terminated | 2026-03-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, CA, DE, ES, NL, QA, SA |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00085412478852 |
| Lot numbers | 60268365, 60268609, 60268610 |
| Model numbers | 100, H93866100 |
| Expiration dates | 2023-10-31 |
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.
Reason for recall
Product is mislabeled as self-righting Luer slip tip caps, yellow.
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-0948-2022. 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.