Recall Z-2462-2016— Biomet 3i, LLC
Class II · Terminated
Class II FDA medical device recall by Biomet 3i, LLC, initiated 2015-11-25, terminated 2019-07-26. FDA's recall record names no specific 510(k) clearance for this event. Product: Drill Stop Dental implants. Reason: Pouches may not have been sealed during packing..
- Recalling firm
- Biomet 3i, LLC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-11-25
- Terminated
- 2019-07-26
- Firm location
- Palm Beach Gardens, FL, United States
Product description
Drill Stop Dental implants
Reason for recall
Pouches may not have been sealed during packing.
Data sourced from openFDA. This site is unofficial and independent of the FDA.