Recall Register

Device recall: MICS3 Angled Sagittal Saw Attachment; Part Number: 210490

Class II FDA enforcement event 98411. Recall start date: . Status in the FDA record: Ongoing.

Reason for recall, in the words of FDA

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.

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

Howmedica Osteonics Corp. started this device recall on 2 Feb 2026. The firm address in the FDA record is in Mahwah, NJ. FDA put the recall in Class II. FDA event 98411 has 1 product record. The first FDA enforcement report date is 25 Mar 2026. The record gives the status Ongoing.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Domestic: Nationwide Distribution; International: Australia, Germany, Belgium, France, Spain UK, New Zealand;

Recalling firm

Howmedica Osteonics Corp., Mahwah, NJ.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 98411: product records
Recall numberProductQuantityClassStatusReport date
Z-1572-2026MICS3 Angled Sagittal Saw Attachment; Part Number: 2104901098 unitsClass IIOngoing25 Mar 2026

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2026
572
Share of these events in Class II
87%
Product records in this event
1Median of the firm: 1
Events of the firm on the register
48

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 98411. https://recallregister.com/fda/ii/98411/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA device enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Domestic: Nationwide Distribution; International: Australia, Germany, Belgium, France, Spain UK, New Zealand;
What quantity of product is in FDA event 98411?
The FDA record gives this quantity: 1098 units
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many device recalls of 2026 have the same class?
87% of the 572 device events that started in 2026 are in Class II.