The Recall Desk
ModerateFDA (Devices)·Z-2424-2016·Announced 2016-08-24

Biomet 3i Recalls Dental Implant O-Ring Abutments Due to Sealing Defect

Biomet 3i is recalling O-Ring Abutments for dental implants because pouches may not have been sealed during packing.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, but the source text describes a packaging defect (unsealed pouches) without reporting any illnesses, injuries, or specific contamination hazards, fitting the criteria for a moderate severity precautionary recall.

Plain-English summary

Biomet 3i, LLC is recalling O-Ring Abutments (4.1mm(D) x 2mm(H), Item: OSO20) used in dental implants. The recall was initiated because the product pouches may not have been sealed during the packing process.

The recall affects 1,648,273 units distributed worldwide, including the United States (nationwide, Hawaii, Guam, Puerto Rico, and the Virgin Islands) and numerous foreign countries. Specific lot numbers subject to the recall include 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.

Dental professionals and patients should check their inventory or records for these specific lot numbers. If the product is identified, it should be removed from use and returned to Biomet 3i, LLC or the distributor in accordance with the recall instructions.

The recalled product

Product
O-Ring Abutment 4.1mm(D) x 2mm(H) Item: OSO20 Dental implants
Manufacturer
Biomet 3i, LLC
Category
Medical Device — Dental Implants
Hazard
Affected units
1,648,273

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

  • Lot # 1002024
  • 1014103
  • 1022623
  • 1030863
  • 1031271
  • 1051924
  • 1054014
  • 1057816
  • 1068294
  • 1069738
  • 1071756
  • 1078857
  • 1082342
  • 1095159
  • 1095387
  • 1129684
  • 1131304
  • 1141288
  • 1161312
  • 1168381

Distribution

Distributed nationwide across the United States.

The notice also names 3 states specifically:

Part of a larger recall action

This product is one of 119 recalled by Biomet 3i, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 119 products in this recall →

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