VeptrRecalls & reported problems across all models
Synthes GmbH · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 94
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 0
We found 2 models of Veptr by Synthes GmbH in the FDA's device registry (GUDID). Together they are named in 94 adverse event reports in the FDA's MAUDE database, received between Jan 3, 2017 and Apr 28, 2026 — classified as 1 injury, 93 malfunctions.
The most frequently reported specific device problem is “Calibration Problem” (79 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Veptr problems
Device problems
- Calibration Problem79
- Device-Device Incompatibility6
- Failure to Calibrate6
- Bent1
- Break1
- Material Integrity Problem1
- No Apparent Adverse Event1
Patient problems
- No Clinical Signs, Symptoms or Conditions44
- No Patient Involvement38
- No Consequences Or Impact To Patient12
- No Code Available1
- No Known Impact Or Consequence To Patient1
Veptr models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Veptr 03.641.004WRENCH86 reports
- Veptr 03.641.003ORTHOPEDIC MANUAL SURGICAL INSTRUMENT8 reports
Recent Veptr adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionApr 28, 2026Calibration Problem
IT WAS REPORTED THAT THE TORQUE TESTING FAILED. THERE WERE NO PATIENT CONSEQUENCES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25017612 ↗MalfunctionOct 16, 2024Calibration Problem; Calibration Problem
IT WAS REPORTED THAT ITEM DID NOT PASS TORQUE TEST INSPECTION. THE TORQUE TEST RESULT IS OUT OF LIMITS. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20466030 ↗MalfunctionOct 11, 2024No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT DURING INSPECTION ON (B)(6) 2024, TWO SOCKET WRENCHES DID NOT PASS THE TORQUE TEST. THIS REPORT IS FOR A SOCKET WRENCH FOR VEPTR NUT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20429213 ↗MalfunctionSep 24, 2024Calibration Problem; Calibration Problem
DURING TODAY¿S INSPECTION, TORQUE TEST DIDN¿T PASS. THE TORQUE TEST WAS NOT WITHIN CORRECT RANGE ON THIS ITEM. THE RANGE SHOULD BE 5,00- 6,40. THIS REPORT INVOLVES ONE SOCKET WRENCH FOR VEPTR NUT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20291380 ↗MalfunctionAug 29, 2024Calibration Problem; Calibration Problem
IT WAS REPORTED THAT ON AUGUST 1, 2024, DURING ROUTINE INCOMING INSPECTION OF A LOANER SET AT HOSPITAL, IT WAS OBSERVED THAT HANDLE, WAS FOUND TO BE OUT OF DRAWING SPECIFICATION. THE TORQUE TESTED HIGH. THERE WAS NO KNOWN PATIENT OR HOSPITAL INVOLVEMENT. THIS REPORT IS FOR ONE (1) SOCKET WRENCH FOR VEPTR NUT. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20098639 ↗MalfunctionAug 26, 2024Calibration Problem; Calibration Problem
IT WAS REPORTED THAT ON (B)(6), 2024, DURING ROUTINE INCOMING INSPECTION OF A LOANER SET, IT WAS OBSERVED THAT THE N.M HANDLE, WAS FOUND TO BE OUT OF DRAWING SPECIFICATION. THE DRAWING SPECIFICATION OF THE TORQUE TESTED HIGH. THERE WAS NO KNOWN PATIENT OR HOSPITAL INVOLVEMENT. ALL INFORMATION REGARDING THIS EVENT HAS BEEN REPORTED. THERE WAS NO PATIENT CONSEQUENCES. THIS REPORT IS FOR ONE (1) SOCKET WRENCH FOR VEPTR NUT. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20071711 ↗MalfunctionFeb 8, 2024Calibration Problem; Calibration Problem
IT WAS REPORTED THAT ON UNKNOWN DATE, DURING ROUTINE INCOMING INSPECTION OF A LOANER SET AT THE SITE, IT WAS OBSERVED THAT MATERIAL 03.641.004, SOCKET WRENCH FOR VEPTR NUT, SN J001347-06 WAS FOUND TO BE OUT OF DRAWING SPECIFICATION. THE DRAWING SPECIFICATION IS 5.0 ¿ 6.4 NM. THE TORQUE TESTED HIGH ¿ 10.61 NM. THERE WAS NO KNOWN PATIENT OR HOSPITAL INVOLVEMENT. THE PRODUCT HAS BEEN QUARANTINED AND IS AVAILABLE AND IS BEING RETURNED TO THE REPAIR SITE. A REPLACEMENT DEVICE HAS BEEN ORDERED. NO REPLACEMENT PRODUCT IS REQUIRED, AND NO SHIPPING LABEL IS REQUIRED FOR THE PRODUCT RETURN. ALL INFORMATION REGARDING THIS EVENT HAS BEEN REPORTED. THERE WERE NO PATIENT CONSEQUENCES REPORTED. THIS REPORT IS FOR ONE (1) SOCKET WRENCH FOR VEPTR NUT. THIS IS REPORT 1 OF 1 FOR COMPLAINT PC-(B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18669997 ↗MalfunctionJan 2, 2024Calibration Problem; Calibration Problem
IT WAS REPORTED THAT ON AN UNKNOWN DATE, DURING ROUTINE INCOMING INSPECTION OF A LOANER SET AT THE DISTRIBUTION CENTER, IT WAS OBSERVED THAT THE SOCKET WRENCH FOR VEPTR NUT WAS OUT OF DRAWING SPECIFICATION. THE TORQUE TESTED HIGH. THERE WAS NO KNOWN PATIENT OR HOSPITAL INVOLVEMENT. THIS REPORT INVOLVES ONE SOCKET WRENCH FOR VEPTR NUT. THIS IS REPORT 1 OF 1 FOR PC-(B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18424505 ↗MalfunctionDec 21, 2023Calibration Problem; Calibration Problem
IT WAS REPORTED THAT ON AN UNKNOWN DATE IN 2023 DURING ROUTINE INCOMING INSPECTION OF A LOANER SET, THE TORQUE WRENCH IN QUESTION WAS FOUND TO BE OUT OF SPEC. THE PRODUCT WAS TESTED USING A CALIBRATED TORQUE METER, THE MEASURED TORQUE VALUE WAS HIGHER THAN THE DRAWING SPECIFICATIONS. THERE WAS NO REPORTED PATIENT OR PROCEDURE INTERACTION. NO FURTHER INFORMATION IS AVAILABLE TO REPORT. THIS REPORT IS FOR A SOCKET WRENCH FOR VEPTR NUT. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18372873 ↗MalfunctionDec 20, 2023Calibration Problem; Calibration Problem
IT WAS REPORTED THAT ON AN UNKNOWN DATE DURING ROUTINE INSPECTION OF A LOANER SET, IT WAS OBSERVED THAT THE SOCKET WRENCH FOR VEPTR NUT WAS FOUND TO BE OUT OF DRAWING SPECIFICATION. THE TORQUE TESTED HIGH. THERE WAS NO KNOWN PATIENT OR HOSPITAL INVOLVEMENT. THIS REPORT INVOLVES ONE SOCKET WRENCH FOR VEPTR NUT. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18367387 ↗MalfunctionDec 20, 2023Calibration Problem; Calibration Problem
IT WAS REPORTED THAT DURING ROUTINE INSPECTION OF A LOANER SET ON AN UNKNOWN DATE, IT WAS NOTED THAT THE SOCKET WRENCH FOR VEPTR NUT WAS FOUND TO BE OUT OF DRAWING SPECIFICATION. THE TORQUE TESTED HIGH. THERE WAS NO KNOWN PATIENT OR HOSPITAL INVOLVEMENT. THIS REPORT INVOLVES ONE SOCKET WRENCH FOR VEPTR NUT. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18367350 ↗MalfunctionJul 24, 2023Calibration Problem; Calibration Problem
IT WAS REPORTED THAT DURING ROUTINE INCOMING INSPECTION OF A LOANER SET, IT WAS OBSERVED THAT THE SOCKET WRENCH FOR VEPTR NUT WAS FOUND TO BE OUT OF DRAWING SPECIFICATION. THE TORQUE TESTED HIGH. THERE WAS NO KNOWN PATIENT OR HOSPITAL INVOLVEMENT. THIS REPORT INVOLVES ONE SOCKET WRENCH FOR VEPTR NUT. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17379496 ↗MalfunctionJun 7, 2023Calibration Problem; Calibration Problem
IT WAS REPORTED THAT ON MAY 23, 2023, DURING ROUTINE INCOMING INSPECTION OF A LOANER SET AT THE MOORESVILLE MD DC, IT WAS OBSERVED THAT THE SOCKET WRENCH FOR VEPTR NUT WAS FOUND TO BE OUT OF DRAWING SPECIFICATION. THERE WAS NO KNOWN PATIENT OR HOSPITAL INVOLVEMENT. THERE WERE NO PATIENT CONSEQUENCES/OUTCOME. THIS COMPLAINT INVOLVES ONE (1) DEVICE. THIS REPORT IS FOR ONE (1) SOCKET WRENCH FOR VEPTR NUT THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17083224 ↗MalfunctionJan 4, 2023Calibration Problem; Calibration Problem
IT WAS REPORTED ON AN UNKNOWN DATE DURING EVALUATION THE REPAIR TECHNICIANS FOUND THAT THE SOCKET WRENCH FOR VEPTR NUT HAD FAILED IN CALIBRATION. ISSUE FOUND DURING TESTING AT SERVICE & REPAIRS/ MONUMENT. NO ADDITIONAL INFORMATION. THERE WAS NO PATIENT INVOLVEMENT. THIS REPORT IS FOR ONE (1) SOCKET WRENCH FOR VEPTR NUT. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16095367 ↗MalfunctionJan 4, 2023Calibration Problem; Calibration Problem
IT WAS REPORTED THAT ON AN UNKNOWN DATE DURING EVALUATION THE REPAIR TECHNICIANS FOUND THAT THIS DEVICE FAILED CALIBRATION. ISSUE FOUND DURING TESTING AT SERVICE AND REPAIR. NO ADDITIONAL INFORMATION. THIS REPORT IS FOR ONE (1) SOCKET WRENCH FOR VEPTR NUT. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16095009 ↗
Other Synthes GmbH products
All Synthes GmbH devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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