Reported Sep 1, 2021 · Terminated

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

BioMimetic Therapeutics, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: BioMimetic Therapeutics, LLC · 389 Nichol Mill Ln # A · Franklin, TN · 37067-4882

Is this the product you have?

    • AUGMENT Injectable Kit
    • 3cc
    • Model K30003010
    • Lot 1706343
Lot codes and dates
    • Model Number K30003010
    • Lot 1706343
Amount recalled
499 units

Where it was sold

Why it was recalled

The kit contains the wrong vial tray in the package.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Sep 4, 2024 · Data as of Sep 19, 4:54 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.