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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/Surgical Equipment

MICS3 Angled Sagittal Saw Attachment Recalled for Detachment Risk

Agency Publication Date: March 18, 2026
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Summary

Howmedica Osteonics Corp. (Stryker) is recalling 1,098 units of the MICS3 Angled Sagittal Saw Attachment due to a defect where external screws can loosen during medical procedures. These screws, which secure the cover to the saw housing, may completely detach from the attachment while the device is in use. Patients and medical staff should be aware that this recall affects all lot numbers for part number 210490 distributed between February and March 2026. Hospitals and surgical centers should immediately identify any affected units in their inventory and contact the manufacturer to arrange for the return or correction of the device.

Risk

The external screws on the saw housing may loosen and fall off during a surgical procedure, potentially causing the device to fail or dropping metal components into a surgical site.

What You Should Do

  1. Stop using the recalled product immediately.
  2. Identify affected units by checking for Part Number 210490 and UDI (01)07613327523874(10)TU6563205RP. This recall affects ALL lot numbers for this part.
  3. Contact Howmedica Osteonics Corp. or your distributor to arrange for the return, replacement, or correction of the attachment.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional questions.

Your Remedy Options

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

Affected Products

Product: MICS3 Angled Sagittal Saw Attachment
Model / REF:
210490
Lot Numbers:
ALL
UDI:
(01)07613327523874(10)TU6563205RP

Recall Number: Z-1572-2026

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98411
Status: Active
Manufacturer: Howmedica Osteonics Corp.
Sold By: Hospital and surgical distributors
Manufactured In: United States
Units Affected: 1098 units
Distributed To: Nationwide

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.