DeRoyal SECURITY CUFFS, Single Strap, QR Buckle Cuff and Bed, UNIVERSAL, REF M8138 - Product Usage: patient restraint.
FDA Recall Z-1604-2020 · Posted None
Advertisement
Recalling FirmDeRoyal Industries Inc
Recall StatusTerminated
Product CodeFMQ
Date Initiated2020-02-27
Date Terminated2022-05-10
Product Quantity94 pairs
Reason for Recall
One lot of product was inadvertently manufactured with a buckle which does not meet the mechanical hold force required for this device.
Firm Action
DeRoyal issued their recall on 2/27/2020 to the end user level by emailing its direct accounts and sales representatives. The customers were asked to identify the affected products, quarantine them, return the affected product and the provided notice of return form back to DeRoyal indicating if replacement or credit is requested. Distributors were asked to further notify their customers. They were asked to do this directly or to provide the recalling firm with a customer listing and the recalling firm would notify them.
Root Cause
Nonconforming Material/Component
Distribution Pattern
VA, CA, FL, AZ
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement