Recall Z-2006-2015— Stradis Healthcare, LLC.

Class II · Completed

Class II FDA medical device recall by Stradis Healthcare, LLC., initiated 2015-04-20. FDA's recall record names no specific 510(k) clearance for this event. Product: Tummy Tuck Pack - contains Devon Light Glove Used during surgery. Reason: Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits..

Recalling firm
Stradis Healthcare, LLC.
Classification
Class II
Status
Completed
Initiated
2015-04-20
Firm location
Lawrenceville, GA, United States

Product description

Tummy Tuck Pack - contains Devon Light Glove Used during surgery

Reason for recall

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

Data sourced from openFDA. This site is unofficial and independent of the FDA.