Hill-Rom Progressa Bed System — Class II medical device recall Z-0231-2023
Ongoing recall by Baxter Healthcare Corporation, reported 2022-11-23, distributed nationwide. The compression links on impacted Progressa beds, listed in Appendix A, may bend when raising the head section
| Recall number | Z-0231-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2022-10-18 |
| Classified | 2022-11-14 |
| Reported by FDA | 2022-11-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, CA, QA, SA, SG |
| Quantity | 248 beds |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00887761000100 |
| Serial numbers | X154AW7288, X154AW7289, X154AW7290, X154AW7291, X154AW7292, X154AW7293, X154AW7294, X154AW7295, X154AW7296, X154AW7297, X154AW7298, X154AW7300, X154AW7301, X154AW7302, X157AW7304, X157AW7305, X157AW7308, X157AW7309, X157AW7311, X157AW7312, X157AW7313, X157AW7316, X157AW7317, X157AW7318, X157AW7320 and 164 more |
Product
Hill-Rom Progressa Bed System
Reason for recall
The compression links on impacted Progressa beds, listed in Appendix A, may bend when raising the head section. The labeling for these beds list a maximum patient weight of 500 lbs., however the bending may still occur with a patient weight of less than 500 lbs. depending on the patient 's position on the bed.
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-0231-2023. 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.