PlainRecalls
FDA Devices Moderate Class II Terminated

AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343

Reported: September 1, 2021 Initiated: July 23, 2021 #Z-2335-2021

Product Description

AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343

Reason for Recall

The kit contains the wrong vial tray in the package.

Details

Units Affected
499 units
Distribution
US Nationwide distribution in the states of AK, CA, CO, FL, GA, IA, ID, IL, IN, MA, MI, MN, NC, NJ, NM, NY, OH, OR, PA, TX, UT, VA, WA, and WI.
Location
Franklin, TN

Frequently Asked Questions

What product was recalled?
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343. Recalled by BioMimetic Therapeutics, LLC. Units affected: 499 units.
Why was this product recalled?
The kit contains the wrong vial tray in the package.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 1, 2021. Severity: Moderate. Recall number: Z-2335-2021.