Recall Z-0693-2023— DeRoyal Industries Inc

Name: FDA recall Z-0693-2023
Creator: U.S. Food and Drug Administration
Published: 2022-11-03

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 LUMBAR DISC PACK, REF 89-10590.02. 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 LUMBAR DISC PACK, REF 89-10590.02

Reason for recall

XXX

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