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Terminated

HoverMatt Patient Transfer Solution/Air Transfer Mattress

FDA Recall Z-0084-06 · Posted 2005-10-21

Recalling FirmD.T. Davis Enterprises Ltd.
Recall StatusTerminated
Product CodeFRZ
Date Initiated2005-09-13
Date Terminated2006-06-07
Product Quantity866 units

Reason for Recall

Instructions for use are not adhering to the product

Firm 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.

Root Cause

Other

Distribution Pattern

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.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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