MAUDE Adverse Event Report: Synthes GmbH PUSH-PULL REDUCTION DEVICE FOR 4.5MM LCP® PLATES; FORCEPS

Catalog Number	311.449
Medical Device Problem Codes	Crack (1135); Material Twisted/Bent (2981); Illegible Information (4050)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/25/2026
Type of Reportable Event	Malfunction

• Brand Name: PUSH-PULL REDUCTION DEVICE FOR 4.5MM LCP® PLATES
• Common Device Name: FORCEPS
• Manufacturer (Section D): Synthes GmbH; eimattstrasse 3; oberdorf 4436 ; SZ 4436
• Manufacturer (Section G): Monument; 1101 synthes avenue; monument CO 80132
• Manufacturer Contact: elba bello ; 1302 wrights lane east; west chester, PA 19380 ; +1(908)386-3534
• MDR Report Key: 50780280
• Report Number: 8030965-2026-09412
• Device Sequence Number: 13431907
• Product Code: HTD
• UDI-Device Identifier: 10886982187437
• UDI-Public: (01)10886982187437
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• PMA/510(K) Number: Exmept
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial

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: 311.449
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Initial Date Received by Manufacturer: 08/25/2026
• Initial Report FDA Received Date: 09/15/2026
• 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
• Patient Sex: Unknown