Severity
Moderate
FDA Devices recall · Reported December 4, 2024
Due to pin coming off of handles.
MicroSurgical Technology Inc recalled Brand Name: MST Duet Reusable Handle for Single Use Heads Product Name: Reusable Handle … - a moderate-severity action.
Brand Name: MST Duet Reusable Handle for Single Use Heads Product Name: Reusable Handle … was recalled by MicroSurgical Technology Inc in December 4, 2024. Reason: Due to pin coming off of handles.. Check the official notice for the remedy. Verify recall #Z-0521-2025 with the FDA Devices before acting.
The recall
MicroSurgical Technology Inc issued this moderate-severity FDA Devices recall-Due to pin coming off of handles..
Sourced from official FDA Devices enforcement records. Verify recall #Z-0521-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Devices action (record #Z-0521-2025) was formally reported on December 4, 2024, with the manufacturer initiating the action on September 17, 2024. It is classified under Moderate severity (Class II), with a current status of Ongoing. MicroSurgical Technology Inc is listed as the recalling firm, operating out of Redmond, WA. Federal records list the affected scope as 24.
The documented reason for this recall is: Due to pin coming off of handles. Distribution data in the federal record shows the product reached: U.S.: CT, GA, MN, MT and TX. O.U.S.: Netherlands 24 total devices = 6 devices distributed in the United States and 18 devices distributed in Germany.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
24
Related Recalls
6
3 from same agency
Brand Name: MST Duet Reusable Handle for Single Use Heads Product Name: Reusable Handle for Single Use Heads (Forceps and Scissors) Model/Catalog Number: DFH-1028 Software Version: N/A Product Description: A MST Single Use Forceps or Scissors System consists of a reusable handle and one of a number of single use interchangeable heads. MST Single Use Forceps and Scissor heads are shipped ready to use sterile in a tray with Tyvek lid within a sterile pouch. MST Duet Reusable Handle for Single Use Forceps & Scissor Heads are supplied in a non-sterile condition and must be sterilized prior to and after every use. The blue sleeve the handle is packaged in is not intended to be sterilized and does not maintain sterility. Component: Yes. The MST Duet¿ Reusable Handle for Single Use Heads is the reusable handle component which connect to either Single Use Forceps or Scissors heads.
Due to pin coming off of handles.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-0521-2025 |
| Date reported | December 4, 2024 |
| Date initiated | September 17, 2024 |
| Recalling firm | MicroSurgical Technology Inc |
| Firm location | Redmond, WA |
| Affected scope | 24 |
| Distribution | U.S.: CT, GA, MN, MT and TX. O.U.S.: Netherlands 24 total devices = 6 devices distributed in the United States and 18 devices distributed in Germany. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported December 4, 2024. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.