MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
MICS3 Angled Sagittal Saw Attachment; Part Number: 210490 was recalled because a potential issue was identified with the torque strength on the external screws of the mics3 angled sagittal saw attachment. these screws, which secure the cover to the angled saw housing, may loosen during use and detach from the attachment.. If you have this product, stop using it until you verify your lot or model details.
By RecallRadar Editorial Team
Sourced from FDA. Last verified April 8, 2026.
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Check if you qualifyKey facts
- Date announced
- March 25, 2026
- Source agency
- FDA
This recall involves safety concerns. Take action promptly.
✨ Plain-English Summary
MICS3 Angled Sagittal Saw Attachment; Part Number: 210490 was recalled because a potential issue was identified with the torque strength on the external screws of the mics3 angled sagittal saw attachment. these screws, which secure the cover to the angled saw housing, may loosen during use and detach from the attachment.. If you have this product, stop using it until you verify your lot or model details.
Is This Recall Still Active?
Status: Yes - Active
This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.
What's Being Recalled
Quoted source excerpt from the official notice.
A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.
Quick Info
Key facts from the official notice, kept in the article flow for easy cross-checking.
- Brand
- Howmedica osteonics corp.
- Category
- medical
- Source agency
- FDA
- Announced
- March 25, 2026
- Country
- US
- Status
- Active
Who's Affected
Specific models and identifiers listed in the source notice:
Model #1
Part Number: 210490; UDI: (01)07613327523874(10)TU6563205RP; Lot numbers: ALL;
| # | Model |
|---|---|
| 1 | Part Number: 210490; UDI: (01)07613327523874(10)TU6563205RP; Lot numbers: ALL; |
Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.
What You Should Do
Follow the remedy path from the official notice using the exact model and serial details above.
- 1Stop using the affected product until you verify whether your item is impacted.
- 2Check the official recall notice and match your model, lot, or serial details.
- 3Follow the official instructions for repair, replacement, refund, or disposal.
Source & Verification
This page summarizes the official notice and keeps key facts easy to verify.
- Official source
- FDA
- Announced by source
- March 25, 2026
- Last reviewed by RecallRadar
- April 8, 2026
Frequently Asked Questions
Am I affected by this recall?
Check the affected models section on this page. The official notice currently lists Part Number: 210490; UDI: (01)07613327523874(10)TU6563205RP; Lot numbers: ALL;.
What is the remedy for this recall?
Follow the official instructions for repair, replacement, refund, or disposal on the howmedica osteonics corp. recall page.
Where can I verify recall details?
Use the official source link in this page to confirm dates, eligibility, and next steps: https://api.fda.gov/device/enforcement.json?search=recall_number:Z-1572-2026&limit=1
Keep browsing with these internal hubs: howmedica osteonics corp. recall hub and Medical recall hub.
Official Resources
Use these primary sources for final eligibility and claim instructions.
View official notice from FDASee an inaccuracy?
Help us improve the accuracy of this recall information.
On this page
Free checker
Check if you qualify
See whether your device may qualify for a free repair or replacement program before you spend money.
Check if you qualifyKey facts
- Date announced
- March 25, 2026
- Source agency
- FDA
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