- Recalling firm
- Baxter Healthcare Corporation
- Reason for recall
- There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product specifications and may lead to incorrect product identification or selection, potentially resulting in use with an incompatible bed frame.
- Affected products (lot / model / serial)
- Serial Number: A171BP3769 - B057BP6765 UDI-DI Number: 00887761007543
- Units affected
- 169 units
- Distribution pattern
- Worldwide distribution - US Nationwide and the country of Canada.
- Firm location
- Deerfield, IL, United States
- Recall type
- Voluntary: Firm initiated
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-3262-2026
- Recall initiated
- August 18, 2026
- FDA classification date
- September 24, 2026
- FDA report date
- September 30, 2026
- FDA event ID
- 99606
- Last updated on HTM Vibe
- October 6, 2026
