MULTILOC 04.017.210SRecalls & reported problems
Synthes GmbH · 7MM TI MULTILOC HUMERAL NAIL LEFT/CANN/210MM-STERILE · Class 2 · Implant
All models of MULTILOC (48)
Data updated Oct 16, 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 10886982089342), received between Oct 21, 2022 and Oct 21, 2022 — classified as 1 injury.
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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Loss of Range of Motion1
- Nonunion/Delayed-union Bone Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 21, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT ON AN UNKNOWN DATE, THERE WAS FRACTURE FIXATION OF THE LONG BONES AND WOUND DEHISCENCE ALSO OCCURRED. POST-OP THE PATIENT EXPERIENCED LIMITED RANGE OF MOTION (ROM), NON-UNION. THE PATIENT DECEASED AT 1 YEAR (NEVER FIXED D/T HEALTH CONCERNS). THIS REPORT INVOLVES ONE (1) 7MM TI MULTILOC HUMERAL NAIL LEFT/CANN/210MM-STERILE. THIS IS REPORT 1 OF 2 FOR (B)(4).
Patient problems: Loss of Range of Motion; Nonunion/Delayed-union Bone Fracture
MAUDE report 15651662 ↗
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- TRIGEN 71674067Smith & Nephew, Inc. · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES201 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-050Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls1 report
- PRECICE Intramedullary Limb Lengthening System LSB5-075Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls0 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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