Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported September 10, 2014
Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# CP751506 The Total Temporomandibular Joint (TMJ) replacement system is implanted in the jaw to functionally reconstruct a diseased and/or damaged temporomandibular joint. The Total TMJ replacement system is a two-component system comprised of mandibular condyle and a glenoid fossa components. Both components are available in multiple stock sizes as right and left specific designs and are attached to the bones
Product mix occurred prior to final package and labeling process.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Biomet Microfixation, LLC recalled Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# CP751… - a moderate-severity action.
Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# CP751… was recalled by Biomet Microfixation, LLC in September 10, 2014. Reason: Product mix occurred prior to final package and labeling process.. Check the official notice for the remedy. Verify recall #Z-2566-2014 with the FDA Devices before acting.
The recall
Biomet Microfixation, LLC issued this moderate-severity FDA Devices recall-Product mix occurred prior to final package and labeling process..
- Moderate
- severity level
- 1 units
- affected scope
- Class II
- classification
- September 10, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2566-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2566-2014) was formally reported on September 10, 2014, with the manufacturer initiating the action on September 20, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Biomet Microfixation, LLC is listed as the recalling firm, operating out of Jacksonville, FL. Federal records list the affected scope as 1.
The documented reason for this recall is: Product mix occurred prior to final package and labeling process. Distribution data in the federal record shows the product reached: Worldwide Distribution to Denmark only.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
1
Related Recalls
6
3 from same agency
Product description
Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# CP751506 The Total Temporomandibular Joint (TMJ) replacement system is implanted in the jaw to functionally reconstruct a diseased and/or damaged temporomandibular joint. The Total TMJ replacement system is a two-component system comprised of mandibular condyle and a glenoid fossa components. Both components are available in multiple stock sizes as right and left specific designs and are attached to the bones by screws.
Reason for recall
Product mix occurred prior to final package and labeling process.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2566-2014 |
| Date reported | September 10, 2014 |
| Date initiated | September 20, 2013 |
| Recalling firm | Biomet Microfixation, LLC |
| Firm location | Jacksonville, FL |
| Affected scope | 1 |
| Distribution | Worldwide Distribution to Denmark only. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2566-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# CP751506 The Total Temporomandibular Joint (TMJ) replacement system is implanted in the jaw to functionally reconstruct a diseased and/or damaged temporomandibular joint. The Total TMJ replacement system is a two-component system comprised of mandibular condyle and a glenoid fossa components. Both components are available in multiple stock sizes as right and left specific designs and are attached to the bones by screws.. Recalled by Biomet Microfixation, LLC. Units affected: 1.
Why was this product recalled? ▼
Product mix occurred prior to final package and labeling process.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 10, 2014. Severity: Moderate. Recall number: Z-2566-2014.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution to Denmark only..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2566-2014) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported September 10, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.