FDA Device recall Z-1468-2025
Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobility, Product Codes…
- FDA Device
- Class II
- ongoing
- Published 2025-04-02
On 2025-04-02 the FDA classified a Class II recall of Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobility, Product Codes… by Baxter Healthcare, citing the air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1468-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-02-25 |
| Published | 2025-04-02 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobility, Product Codes P7520A19, P7520A20S, P7520A21, P7520A22S, P7520A23, P7520A24S, P7520A3, P7520A31, P7520A37, P7520A39, P7520A45, and P7520A4S.
Reason
The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.
Identifiers
| code_info | P7520A19 UDI-DI: 00887761999893; P7520A20S UDI-DI: 00887761999886; P7520A21 UDI-DI: 00887761999879; P7520A22S UDI-DI: 0…P7520A19 UDI-DI: 00887761999893; P7520A20S UDI-DI: 00887761999886; P7520A21 UDI-DI: 00887761999879; P7520A22S UDI-DI: 00887761999862; P7520A23 UDI-DI: 00887761999855; P7520A24S UDI-DI: 00887761999848; P7520A3 UDI-DI: 00887761999770; P7520A31 UDI-DI: 00887761999756; P7520A37 UDI-DI: 00887761999718; P7520A39 UDI-DI: 00887761999701; P7520A45 UDI-DI: 00887761999671; P7520A4S UDI-DI: 00887761999657; Serial Numbers: A008MW1489 Y298MW1411 Y298MW1412 Y298MW1413 Y298MW1414 Y298MW1415 Y298MW1416 Y298MW1417 Y298MW1418 Y298MW1419 Y298MW1420 Y298MW1421 Y298MW1452 Y298MW1453 Y298MW1454 Y298MW1455 Y298MW1456 Y298MW1457 Y298MW1458 Y298MW1459 Y298MW1460 Y298MW1461 Y298MW1463 Y298MW1464 Y298MW1465 Y298MW1466 Y298MW1467 Y298MW1468 Y298MW1469 Y298MW1470 Y298MW1471 Y298MW1472 Y298MW1473 Y298MW1474 Y298MW1475 Y298MW1580 Y298MW1581 Y298MW1582 Y298MW1583 Y298MW1584 Y298MW1585 Y298MW1586 Y298MW1587 Y298MW1588 Y298MW1589 Y298MW1590 Y298MW1591 Y298MW1592 Y298MW1593 Y298MW1594 Y298MW1595 Y298MW1596 Y298MW1597 Y |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1468-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.