Recall Z-0601-2023— DeRoyal Industries Inc

Class II · Ongoing

Class II FDA medical device recall by DeRoyal Industries Inc, initiated 2022-11-03. FDA's recall record names no specific 510(k) clearance for this event. Product: DeRoyal ORTHO SPINE BACK PACK, REF 89-7534.09. Reason: XXX.

Recalling firm
DeRoyal Industries Inc
Classification
Class II
Status
Ongoing
Initiated
2022-11-03
Firm location
Powell, TN, United States

Product description

DeRoyal ORTHO SPINE BACK PACK, REF 89-7534.09

Reason for recall

XXX

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