D.T. Davis Enterprises Ltd. HoverMatt Patient Transfer Solution/Air Transfer Mattress Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
HoverMatt Patient Transfer Solution/Air Transfer Mattress
Brand
D.T. Davis Enterprises Ltd.
Lot Codes / Batch Numbers
Model Numbers HM28HS, HM28DC, HM34HS, HM34DC, HM39HS, HM39DC
Products Sold
Model Numbers HM28HS, HM28DC, HM34HS, HM34DC, HM39HS, HM39DC
D.T. Davis Enterprises Ltd. is recalling HoverMatt Patient Transfer Solution/Air Transfer Mattress due to Instructions for use are not adhering to the product. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Instructions for use are not adhering to the product
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026