NA 04.641.117Recalls & reported problems
Synthes GmbH · TI DISTAL EXTENSION SIZE 7/220MM RADIUS · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034750521), received between Apr 1, 2019 and Apr 1, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (1 report).
1 other recall cover devices cleared under the same FDA submission (K142587); they may or may not involve this specific model.
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- Discomfort1
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 1, 2019Break; Break
04/23/2019: UPDATED EVENT DESCRIPTION: IT WAS REPORTED THAT ON (B)(6) 2019, THE PATIENT UNDERWENT A REVISION SURGERY FOR A FAILED VERTICAL EXPANDABLE PROSTHETIC TITANIUM RIB (VEPTR) TITANIUM DISTAL EXTENSION, TITANIUM PROXIMAL EXTENSION AND TITANIUM DISTRACTION LOCK, THESE DEVICES HAVE BREAKAGE/FRACTURE. THE PATIENT PRESENTED WITH SOME DISCOMFORT. X-RAYS REVEALED SPLAYING OF THE RAILS OF THE PROXIMAL EXTENSION. THE PATIENT ALSO WAS ABOUT TO OUTGROW HIS EXTENSION ON THE CONTRA-LATERAL SIDE, SO SURGERY WAS SCHEDULE TO REPLACE BOTH SIDES. THERE WAS PATIENT CONSEQUENCE DUE TO MYELOMENIGOCELE. PROCEDURE OUTCOME IS UNKNOWN. THE PATIENT EXPOSED TO ADDITIONAL ANESTHESIA FOR ONE (1) HOUR. CONCOMITANT DEVICE REPORTED: TI DISTRACTION LOCK (PART # 497.125, LOT # H468144, QUANTITY # 1) UNK - RODS: SPINE (PART # UNKNOWN, LOT # UNKNOWN # QUANTITY # UNKNOWN). THIS COMPLAINT INVOLVES TWO (2) DEVICES.
Patient problems: Discomfort; No Code Available
MAUDE report 8470899 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K142587. One submission often covers many models, so check the product and lot details in each record.
- Z-2488-2015 · Jul 29, 2015 · TerminatedVEPTR Vertical Expandable Prosthetic Titanium Rib, inferior cradles also known as caudal rib supports. The VEPTR/VEPTR II devices mechanically stabilize and/or correct thoracic de
Other Prosthesis, rib replacement devices
- NA 04.641.002Synthes GmbH · Prosthesis, rib replacement4 reports
- NA 04.641.114Synthes GmbH · Prosthesis, rib replacement1 report
- NA 04.641.079Synthes GmbH · Prosthesis, rib replacement1 report
- NA 04.641.057Synthes GmbH · Prosthesis, rib replacement1 report
- NA 497.108Synthes GmbH · Prosthesis, rib replacement1 report
- NA 04.641.056Synthes GmbH · Prosthesis, rib replacement1 report
- NA 04.641.115Synthes GmbH · Prosthesis, rib replacement1 report
- NA 04.641.113Synthes GmbH · Prosthesis, rib replacement1 report
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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