Reported Aug 24, 2016 · Terminated

O-Ring Abutment 4.1mm(D) x 2mm(H) Item: OSO20 Dental implants

Biomet 3i, 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: Biomet 3i, LLC · 4555 Riverside Dr · Palm Beach Gardens, FL · 33410-4200

Is this the product you have?

  • O-Ring Abutment 4.1mm(D)
  • x 2mm(H) ItemOSO20 Dental implants
Lot codes and dates
    • Lot # 1002024
    • 1014103
    • 1022623
    • 1030863
    • 1031271
    • 1051924
    • 1054014
    • 1057816
    • 1068294
    • 1069738
    • 1071756
    • 1078857
    • 1082342
    • 1095159
    • 1095387
    • 1129684
    • 1131304
    • 1141288
    • 1161312
    • 1168381
    • 1169242
    • 1169931
    • 1170162
    • 1173357
    • 987787
    • and 987884
Amount recalled
1,648,273 (all products subject to these recall)

This recall covers 119 products

The agency filed one notice per product. You are reading one of them; the other 118 are below.

106 more are in the archive.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Pouches may not have been sealed during packing.

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

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Jul 26, 2019 · Data as of Sep 19, 5:21 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.