Argus PB-3000 — Class II medical device recall Z-2672-2025
Ongoing recall by Schiller, Ag, reported 2025-10-08, distributed nationwide. Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specificall
| Recall number | Z-2672-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Schiller, Ag, Baar, N/A, Switzerland |
| Recall initiated | 2025-08-08 |
| Classified | 2025-09-29 |
| Reported by FDA | 2025-10-08 |
| Distributed | Nationwide (US) |
| Quantity | 266 units |
| UPC / GTIN / UDI-DI | 07613365000115, 07613365001914, 07613365003024, 07613365003468, 07613365003475 |
| Serial numbers | 7010.000160 |
| Model numbers | 1A.701307, 3.921002, 3.921006, 3.921030, 3.921031 |
Product
Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006
Reason for recall
Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.
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-2672-2025. 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.