FDA Device recall Z-0231-2023
Hill-Rom Progressa Bed System
- FDA Device
- Class II
- ongoing
- Published 2022-11-23
On 2022-11-23 the FDA classified a Class II recall of Hill-Rom Progressa Bed System by Baxter Healthcare, citing 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 lb….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0231-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-10-18 |
| Published | 2022-11-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Hill-Rom Progressa Bed System
Reason
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.
Identifiers
| code_info | UDI/DI 00887761000100, Serial Numbers: X157AW7312, X206AW8017, X154AW7292, X166AW7416, X207AW8041, X158AW7351, X157AW7…UDI/DI 00887761000100, Serial Numbers: X157AW7312, X206AW8017, X154AW7292, X166AW7416, X207AW8041, X158AW7351, X157AW7326, X157AW7313, X206AW8018, X154AW7293, X166AW7418, X167AW7449, X158AW7352, X157AW7328, X174AW7575, X206AW8019, X154AW7296, X167AW7428, X167AW7450, X158AW7353, X157AW7329, X174AW7579, X206AW8021, X154AW7297, X167AW7429, X167AW7451, X158AW7354, X157AW7330, X181AW7722, X206AW8022, X154AW7298, X157AW7308, X166AW7419, X158AW7355, X157AW7332, X181AW7728, X206AW8023, X154AW7300, X157AW7309, X167AW7425, X206AW8010, X158AW7340, X182AW7736, X206AW8024, X168AW7456, X178AW7622, X167AW7427, X206AW8011, X158AW7341, X182AW7737, X206AW8025, X168AW7478, X178AW7623, X159AW7375, X206AW8012, X158AW7342, X207AW8060, X158AW7344, X171AW7495, X178AW7625, X159AW7378, X206AW8020, X158AW7343, X208AW8079, X206AW8026, X171AW7496, X178AW7626, X159AW7380, X158AW7333, X158AW7349, X208AW8082, X206AW8027, X171AW7497, X178AW7627, X216AW8193, X158AW7334, X158AW7359, X208AW8084, X206AW8028, X171AW7498, |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0231-2023%22
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