Recall Z-0706-2020— DeRoyal Industries Inc

Name: FDA recall Z-0706-2020
Creator: U.S. Food and Drug Administration
Published: 2019-11-21

Class II · Ongoing

Class II FDA medical device recall by DeRoyal Industries Inc, initiated 2019-11-21. FDA's recall record names no specific 510(k) clearance for this event. Product: DeRoyal KNEE BRACE, WARRIOR RECOVERY: 1) REF KB9000-01 2) REF 11-450A-00 3) REF 1150UTPP. Reason: The Warrior Recovery Knee Brace has the potential to come apart due to the hinge breaking..

Recalling firm: DeRoyal Industries Inc
Classification: Class II
Status: Ongoing
Initiated: 2019-11-21
Firm location: Powell, TN, United States

Product description

DeRoyal KNEE BRACE, WARRIOR RECOVERY: 1) REF KB9000-01 2) REF 11-450A-00 3) REF 1150UTPP

Reason for recall

The Warrior Recovery Knee Brace has the potential to come apart due to the hinge breaking.

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