MAUDE Adverse Event Report: SYNTHES GMBH T25 SDDRIVE SCREWDRIVER SHAFT 241MM

Catalog Number	03.168.014
Medical Device Problem Code	Material Twisted/Bent (2981)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/24/2026
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that retent pin scrdriver qc hex 12/sht/xl25, t15 cann strdrv scrwdrvr sft slf-retain, 2.7mm cann drill bit qc/145mm, scrdriver-hex-small w/hold-sleeve, monobloc flexible reamer 14 - std - dd, monobloc flex reamer 14.5 - long - dd, drive shaft for ria 2 520mm, t25 sddrive screwdriver shaft 241mm, and torque limiting attachment 4nm for ao reaming coupler were reported as damaged during post-operative inspection.The failures included broken tips, stripped features, rust inside cannulas, and non-functioning torque limiter.There was no patient involvement or harm, and no procedure was associated with the event.
Additional Manufacturer Narrative
Product complaint # (b)(4) this report is being submitted pursuant to the provisions of 21 cfr, part 803 (and/or part 4, as applicable).This report may be based on information which has not been investigated or verified prior to the required reporting date.This report does not reflect a conclusion by depuy synthes, or its employees that the report constitutes an admission that the product, depuy synthes, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.H11 additional manufacturer narrative: d4: udi: as the lot number for the device involved in the event was not provided, the full udi is currently not available.
Additional Manufacturer Narrative
Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.If the information is unknown, not available or does not apply, the section/field of the form is left blank.H11 additional narrative: added: d10 if information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Additional Manufacturer Narrative
Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.If the information is unknown, not available or does not apply, the section/field of the form is left blank.H11 additional narrative: h6 component codes: most relevant component code is g07002 (appropriate term/code not available) to capture no findings available due to no product returned.Investigation summary.Product was not returned.Based on the information available, it has been determined that no corrective and preventative action is proposed.This complaint will be accounted for and monitored via post market surveillance activities.If additional information is made available, the investigation will be updated as applicable.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

• Brand Name: T25 SDDRIVE SCREWDRIVER SHAFT 241MM
• Common Device Name: SCREWDRIVER
• Manufacturer (Section D): SYNTHES GMBH; luzernstrasse 19-21; zuchwil 4528 ; SZ 4528
• Manufacturer (Section G): MONUMENT; 1101 synthes avenue; monument CO 80132
• Manufacturer Contact: elba bello ; 1302 wright lane east; west chester, PA 19380 ; 9083863534
• MDR Report Key: 24533375
• Report Number: 8030965-2026-02304
• Device Sequence Number: 8933747
• Product Code: HXX
• UDI-Device Identifier: 10886982274489
• UDI-Public: (01)10886982274489
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup

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 Number: 03.168.014
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 02/23/2026
• Supplement Date Received by Manufacturer: 03/13/2026; 03/26/2026
• Initial Report FDA Received Date: 03/06/2026
• Supplement Report FDA Received Date: 03/26/2026; 03/30/2026
• 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: Unknown
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 2.7MM CANN DRILL BIT QC/ 145MM; 511.774; DRIVE SHAFT FOR RIA 2 520MM; MONOBLOC FLEX REAMER 14.5 - LONG - DD; MONOBLOC FLEXIBLE REAMER 14 - STD - DD; RETENT PIN SCRDRIVER QC HEX 12/SHT/XL25; SCRDRIVER-HEX-SMALL W/HOLD-SLEEVE; T15 CANN STRDRV SCRWDRVR SFT SLF-RETAIN; T15 CANN STRDRV SCRWDRVR SFT SLF-RETAIN; T25 SDDRIVE SCREWDRIVER SHAFT 241MM
• Patient Sex: Unknown