Reported Feb 19, 2020 · Terminated

Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010

Medicrea International

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: Medicrea International · 5389 Route De Strasbourg · Rillieux La Pape · N/A

Is this the product you have?

  • Medicrea TLIF-B Holder, short intended for Intervertebral
  • body fusion device CatalogNumber A24200010
Lot codes and dates
    • Lot Numbers l9B0570
    • 19B0572
Amount recalled
14 units

Where it was sold

Why it was recalled

Inner draw rod, which threads into the cage may potentially be separated from the proximal knob of the inserter

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 Feb 8, 2021 · Data as of Sep 19, 4:53 PM UTC

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