Welch Allyn Life2000 Compressor — Class I medical device recall Z-1726-2025
Ongoing recall by Baxter Healthcare Corporation, reported 2025-05-21. A cybersecurity vulnerability was discovered through internal testing.
| Recall number | Z-1726-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2025-04-07 |
| Classified | 2025-05-09 |
| Reported by FDA | 2025-05-21 |
| Quantity | 4,174 units |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 00815410020292, 00815410020537, 00887761976283, 00887761978041, 00887761978072 |
Product
Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.
Reason for recall
A cybersecurity vulnerability was discovered through internal testing.
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-1726-2025. 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.