Biomet Microfixation Recalls Total Temporomandibular Joint Replacement Systems
Biomet Microfixation is recalling 42 total temporomandibular joint replacement systems because laser etching on the parts is wider and deeper than previously validated conditions.
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. The hazard involves a manufacturing deviation (laser etching dimensions) without reported injuries or illnesses, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Biomet Microfixation, LLC is recalling 42 units of the Total Temporomandibular Joint Replacement System (Model 24-6645TI). The recall involves specific lot numbers: 472580A, 472590B, 472580B, 472590A, 526030A, 526020A, 526020B, and 526030B.
The recall was initiated because the laser etching on the parts is wider and deeper than the conditions previously validated. The affected devices were distributed worldwide, including in the United States (Pennsylvania, Minnesota, California) and internationally to Australia, the Netherlands, France, and the United Kingdom.
Healthcare providers and patients should contact Biomet Microfixation, LLC for instructions on how to handle the recalled devices. The source text does not report any illnesses or injuries associated with this recall.
The recalled product
- Product
- Total Temporomandibular Joint Replacement System- 45mm Rt Stand Off TI Mand Reconstruction of the temporomandibular joint
- Manufacturer
- Biomet Microfixation, LLC
- Hazard
- Affected units
- 42
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 (9)
- Model 24-6645TI
- Lot #s: 472580A
- 472590B
- 472580B
- 472590A
- 526030A
- 526020A
- 526020B
- 526030B
Distribution
Part of a larger recall action
This product is one of 14 recalled by Biomet Microfixation, 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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