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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Implants & Prosthetics

BEAR Implant Recalled for Incorrect Expiration Date on Label

Agency Publication Date: January 29, 2026
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Summary

Miach Orthopaedics is recalling 284 units of the BEAR Implant, Model Number 1000, because the labels feature an incorrect expiration date that extends beyond the product's documented and approved shelf life. Because the expiration date is incorrect, the Unique Device Identifier (UDI) on the packaging is also incorrect. This recall affects implants distributed across 22 states between December 2025 and January 2026.

Risk

The incorrect expiration date may lead healthcare providers to use the implant after its validated shelf life, which could compromise the device's performance or sterility. No specific injuries have been reported to date.

What You Should Do

  1. Identify if you have the affected BEAR Implant by checking the packaging for Model Number 1000 and Lot Number 7011098.
  2. Verify the expiration date printed on the label; the affected units incorrectly state an expiration date of 02/28/2026.
  3. Stop using the recalled device immediately.
  4. Contact Miach Orthopaedics or your distributor to arrange for the return, replacement, or correction of the affected product.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional questions regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: BEAR Implant
Model / REF:
1000
Lot Numbers:
7011098 (Exp 02/28/2026)
UDI:
00860002987804

With an incorrect expiration date, the UDI will also be incorrect.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98280
Status: Active
Manufacturer: Miach Orthopaedics
Sold By: Hospital and clinical supply chains
Manufactured In: United States
Units Affected: 284 units
Distributed To: Alaska, California, Colorado, Connecticut, Florida, Georgia, Illinois, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, North Carolina, New Jersey, New York, Ohio, Oregon, Texas, Virginia, Washington, Wisconsin
Agency Last Updated: February 3, 2026

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.