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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: TORNIER INC PERFORM HUMERAL IMPACTOR TIP SIZE 1/2

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TORNIER INC PERFORM HUMERAL IMPACTOR TIP SIZE 1/2 Back to Search Results
Catalog Number MWM051
Medical Device Problem Codes Break (1069); Fracture (1260)
Health Effect - Clinical Code Insufficient Information (4580)
Date of Event 08/01/2025
Type of Reportable Event Malfunction
Event or Problem Description
It was reported that the humeral size 1-2 impactor tip broke.
 
Additional Manufacturer Narrative
A supplemental report will be submitted if additional information becomes available.
 
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Brand Name
PERFORM HUMERAL IMPACTOR TIP SIZE 1/2
Common Device Name
IMPACTOR
Manufacturer (Section D)
TORNIER INC
10801 nesbitt avenue s
bloomington MN 55437
Manufacturer (Section G)
TORNIER INC
10801 nesbitt avenue s
bloomington MN 55437
Manufacturer Contact
dannielle stap
325 corporate drive
mahwah, NJ 07430
2018315000
MDR Report Key22922069
Report Number0001649390-2025-00605
Device Sequence Number9116471
Product Code HWA
UDI-Device Identifier00846832082841
UDI-Public00846832082841
Combination Product (Y/N)N
Initial Reporter StateMA
Initial Reporter CountryUS
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Company Representative
Initial Reporter Occupation Other
Type of Report Initial
Report Date (Section B) 08/29/2025
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Catalogue NumberMWM051
Device Lot NumberUNKNOWN
Was Device Available for Evaluation? No
Type of Report(Section G)Initial
Initial Date Received by Manufacturer 08/01/2025
Initial Report FDA Received Date08/29/2025
Was Device Evaluated by Manufacturer? (Y/N) No
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Reuse
Patient Sequence Number1
Patient SexUnknown
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