BioMimetic Therapeutics, LLC AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
Brand
BioMimetic Therapeutics, LLC
Lot Codes / Batch Numbers
Model Number K30003010, Lot 1706343
Products Sold
Model Number K30003010, Lot 1706343
BioMimetic Therapeutics, LLC is recalling AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343 due to The kit contains the wrong vial tray in the package.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The kit contains the wrong vial tray in the package.
Recommended Action
Per FDA guidance
Recall communication was sent out via FedEx Priority Overnight. Customers are instructed to immediately quarantine all recalled products they have and return all affected product to the recalling firm's Arlington, TN Warehouse as soon as possible. If they have further distributed the affected product, they are instructed to notify the applicable parties at once about this recall. They may copy and distribute the notification letter and the recalling firm will work directly with them to collect the recalled items.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026