Reported Feb 26, 2020 · Terminated

Abutment Screw Retrieval Kit - Product Usage: The kit itself does not have a specific intended Use, but included…

Nobel Biocare USA 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: Nobel Biocare Usa Llc · 22715 Savi Ranch Pkwy · Yorba Linda, CA · 92887-4609

Is this the product you have?

  • Abutment
  • Screw Retrieval Kit - Product UsageThe kit itself does not have a specific intended Use, but included devices have specific intended use as shown above
Lot codes and dates
  • (01)07332747083866(10)818727 (01)07332747083866(10)818683 Catalog# 37481
Amount recalled
7 units

This recall covers 24 products

The agency filed one notice per product. You are reading one of them; the other 23 are below.

11 more are in the archive.

Where it was sold

Why it was recalled

Due to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall remain sterile during their shelf-life.

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 15, 2024 · Data as of Sep 19, 4:51 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.