NA 698335409Recalls & reported problems
Depuy Spine, LLC · MODIFIED INSTRUMENT BENDER TIP, B 5 DEGREES · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034371139), received between Jun 28, 2024 and Jun 28, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 28, 2024Break; Material Deformation; Break; Material Deformation
IT WAS REPORTED DURING SURGERY ON (B)(6) 2024, THE TIP OF INSTRUMENT BROKE DURING SURGERY. IT IS A "ROD BENDER" TIP AND IT BROKE DURING THE ROD BENDING PROCESS. NO INCIDENT OR FRAGMENTS REPORTED. NO SURGICAL DELAY. THE TIP OF A SIMILAR INSTRUMENT IS ALSO BENT OUT OF SHAPE FOLLOWING REPEATED USE OVER THE YEARS. ANOTHER "TIP" WAS USED. THE BROKEN/DAMAGED ONES ARE 5 DEGREE TIPS, SO SURGERY WAS COMPLETED USING 10 DEGREE TIPS. PROCEDURE WAS COMPLETED SUCCESSFULLY. THIS REPORT IS FOR MOD BENDER TIP-B, 5.5MM, 5 DEG THIS IS REPORT 2 OF 2 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19638068 ↗
Other BENDER devices
- MONARCH 277030000Depuy Spine, LLC · BENDER15 reports
- EXPEDIUM 299704190Medos International Sàrl · BENDER9 reports
- EXPEDIUM 299704200Medos International Sàrl · BENDER9 reports
- EXPEDIUM 299704195Medos International Sàrl · BENDER9 reports
- EXPEDIUM 299704185Medos International Sàrl · BENDER8 reports
- ALTALYNE 5161-04-1700Medos International Sàrl · BENDER8 reports
- NA 03.161.057Synthes GmbH · BENDER5 reports
- EXPEDIUM 279763865Medos International Sàrl · BENDER4 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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