Recall Z-2110-2017— Molnlycke Health Care, Inc
Class II · Ongoing
Class II FDA medical device recall by Molnlycke Health Care, Inc, initiated 2017-04-24. FDA's recall record names no specific 510(k) clearance for this event. Product: Brennen Skin Graft Mesher. Surgical instrument designed to expand skin grafts'. Reason: Sterilization validation failure..
- Recalling firm
- Molnlycke Health Care, Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2017-04-24
- Firm location
- Norcross, GA, United States
Product description
Brennen Skin Graft Mesher. Surgical instrument designed to expand skin grafts'
Reason for recall
Sterilization validation failure.
Data sourced from openFDA. This site is unofficial and independent of the FDA.