Loading...
Loading...
All product recalls associated with Biomet Microfixation, Inc..
Total Recalls
1000
Past Year
566
Class I (Serious)
25
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The outer foil pouch on the Lactosorb Plate system was not properly sealed. The product is labeled as sterile, but the lot was not sterilized. These devices are intended to be implanted into bone and are required to be sterile. A heavy bioburden would increase the potential for bone infection (osteomyelitis).
Some product ROM cards have an incorrect program loaded and are unable to be updated.
Mislabeling: The part number on the product label packaging may not match the product.