Recall Z-2335-2021— BioMimetic Therapeutics, LLC
Class II · Terminated
Class II FDA medical device recall by BioMimetic Therapeutics, LLC, initiated 2021-07-23, terminated 2024-09-04. FDA's recall record names no specific 510(k) clearance for this event. Product: AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343. Reason: The kit contains the wrong vial tray in the package..
- Recalling firm
- BioMimetic Therapeutics, LLC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-07-23
- Terminated
- 2024-09-04
- Firm location
- Franklin, TN, United States
Product description
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
Reason for recall
The kit contains the wrong vial tray in the package.
Data sourced from openFDA. This site is unofficial and independent of the FDA.