Compella Bariatric Bed System — Class II medical device recall Z-0820-2022
Terminated recall by Baxter Healthcare Corporation, reported 2022-03-30, distributed nationwide. Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of sh
| Recall number | Z-0820-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2022-02-14 |
| Classified | 2022-03-23 |
| Reported by FDA | 2022-03-30 |
| Terminated | 2026-07-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, BH, BM, BR, BS, CA, CH, DE, EE, ES, FI, FR, GB, GR, HU, IE, IN, IT, JM, JO, KW, MX, NL, NO, NZ, OM, PL, QA, RO, SA, SE, TH, ZA |
| Quantity | 5,186 units |
| UPC / GTIN / UDI-DI | 00887761000902 |
Product
Compella Bariatric Bed System
Reason for recall
Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.
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-0820-2022. 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.