Baxter DISCPAC Syringe Tip Caps — Class II medical device recall Z-1579-2022
Ongoing recall by Baxter Healthcare Corporation, reported 2022-08-31, distributed nationwide. There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
| Recall number | Z-1579-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2022-07-22 |
| Classified | 2022-08-25 |
| Reported by FDA | 2022-08-31 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, DE, ES, FI, GB |
| Quantity | 168,390 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00085412478944, 00085412479811, 00085412479965 |
| Model numbers | H938674100, H93869025, H93869100 |
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Green: a) 25 pack, REF H93869025, b) 100 pack, REF H938674100, c) 100 pack, REF H93869100
Reason for recall
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
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-1579-2022. 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.