FDA Medical Device Recalls (openFDA)
D.T. Davis Enterprises Ltd.: HoverMatt Patient Transfer Solution/Air Transfer Mattress
- Recall number
- Z-0084-06
- Recalling firm
- D.T. Davis Enterprises Ltd.
- Product
- HoverMatt Patient Transfer Solution/Air Transfer Mattress
- Status
- Terminated
- Initiated
- 2005-09-13
- Posted
- 2005-10-21
- Terminated
- 2006-06-07
- Reason
- Instructions for use are not adhering to the product
- Root cause
- Other
- Action
- Recalling firm issued recall letters dated October 5, 2005 informing the hospitals of the problem and that firm representatives would contact them to visit their facilities to affix new labels.
- Quantity
- 866 units
- Distribution
- Products were shipped to hospitals nationwide. Product was also shipped to Canada, Australia, and the United Kingdom.Product was shipped to government accounts in TN, PA, and CA.
- Lot, serial or model codes
- Model Numbers HM28HS, HM28DC, HM34HS, HM34DC, HM39HS, HM39DC
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FRZ
- Firm FEI
- 3001600982
- Firm city
- Bethlehem
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28