Recall Z-2489-2021— 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: Bone Marrow Transplantation biopsy needle. 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
Bone Marrow Transplantation biopsy needle
Reason for recall
Sterility assurance may be compromised.
Data sourced from openFDA. This site is unofficial and independent of the FDA.