Recall Z-0084-06 ยท FRZ Device, Patient Transfer, Powered
D.T. Davis Enterprises Ltd.
HoverMatt Patient Transfer Solution/Air Transfer Mattress
| Date | Oct 21, 2005 (initiated Sep 13, 2005) |
| Status | Terminated |
| 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. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.