Recall Z-0665-2023— 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 BIOPSY PACK, REF 89-9739.06. 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 BIOPSY PACK, REF 89-9739.06

Reason for recall

XXX

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