Biomet 3i Recalls IOL Titanium Temporary Cylinder Dental Implants
Biomet 3i, LLC is recalling IOL Titanium Temporary Cylinder Dental implants because pouches may not have been sealed during packing.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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. The hazard is a packaging defect (unsealed pouches) which is a low-risk contamination or labeling/packaging issue, fitting the 'Moderate' criteria for minor labeling/packaging errors or low-risk contamination without reported injuries.
Plain-English summary
Biomet 3i, LLC is recalling IOL Titanium Temporary Cylinder Dental implants (Item: IOLTC) because the pouches containing the devices may not have been sealed during packing. The recall covers 1,648,273 devices.
The affected products were distributed worldwide, including in the United States (nationwide, Hawaii, Guam, Puerto Rico, and the Virgin Islands) and numerous foreign countries. The source text does not specify which specific foreign countries received the affected units, though a list of foreign consignees is provided in the structured data.
Consumers and healthcare providers should stop using these devices and contact Biomet 3i, LLC for instructions on how to return or replace the affected implants.
The recalled product
- Product
- IOL Titanium Temporary Cylinder Dental implants
- Manufacturer
- Biomet 3i, LLC
- Category
- Medical Device — Dental Implants
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 (1)
- Item: IOLTC
Distribution
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.
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