BEAR Implant (Miach Orthopaedics) – Limited Field Action (2023)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BEAR Implant (Bridge-Enhanced ACL Restoration); Model/Catalog: 1000;
Brand
Miach Orthopaedics
Lot Codes / Batch Numbers
Model/Catalog: 1000, UDI-DI: 00860002987804, Lot number: 7008409
Products Sold
Model/Catalog: 1000; UDI-DI: 00860002987804; Lot number: 7008409;
Miach Orthopaedics is recalling BEAR Implant (Bridge-Enhanced ACL Restoration); Model/Catalog: 1000; due to The field action was initiated in February of 2023 and was limited to the affected lot from sales force trunk stock only.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The field action was initiated in February of 2023 and was limited to the affected lot from sales force trunk stock only.
Recommended Action
Per FDA guidance
On January 30, 2023 RE: BEAR Implant Hydration memo emails were sent to sales staff. If you observe an implant that hydrates too quickly (e.g., less than 30 seconds) and appears that it may not remain intact upon insertion into the knee, do not attempt to implant the device. We would recommend you always have a backup device available to address such circumstances. We plan to revise the Tips and Pearls document, ML-1027, to provide further instructions/details on how to properly hydrate the BEAR device. In the meantime, one way to avoid shortened hydration time is to consider hydrating the dense side of the implant first and continue toward the porous side . To date, all reports of this observation have involved Lot # 7008409. As a precaution and to ensure customer satisfaction, we are asking that you return all devices from this lot that are currently in your trunk stock (in your possession). Chris Brown will work with you to coordinate returns as well as replacing these trunk stock devices. Please contact me (mohara@miachortho.com) or Arjun (aishwar@miachortho.com) if you have questions.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026