Recall Z-2491-2021— M.D.L. S.r.l.

Class II · Completed

Class II FDA medical device recall by M.D.L. S.r.l., initiated 2021-08-05. FDA's recall record names no specific 510(k) clearance for this event. Product: Mammary Nodules Localization. Reason: Sterility assurance may be compromised..

Recalling firm
M.D.L. S.r.l.
Classification
Class II
Status
Completed
Initiated
2021-08-05
Firm location
Delebio, Italy

Product description

Mammary Nodules Localization

Reason for recall

Sterility assurance may be compromised.

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