inforMED
MalfunctionHXP

Bend Press L400

Received Jul 27, 2026 · Event occurred Jan 1, 2026

Report 8030965-2026-07644 · MDR key 50020197

Device

Generic name

Instr,bending Or Contouring

Manufacturer

Synthes Gmbh

Catalog number

329.300

Lot number

7647P33

Product problems

  • Device-Device Incompatibility
  • Material Deformation

Patient

Not reported

  • No Clinical Signs, Symptoms or Conditions

Narrative

Description of Event or Problem

It was reported the tip screw of the bending press is bent and unable to engage with the anvil. No further information is available.

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 MedWatch, a Follow-up MedWatch will be filed as appropriate.