LCP 241.683Recalls & reported problems
Synthes GmbH · 2.4MM LCP® RADIAL HEAD RIM PLATE 3 HOLES-LEFT · Class 2 · Implant
All models of LCP (367)
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 10886982167491), received between Jul 6, 2022 and Jul 6, 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
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 6, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT ON (B)(6) 2022, THE REVISION RADIAL HEAD PROCEDURE, THE REMOVAL OF PLATE 3 HOLES LEFT ALSO REMOVAL OF SCREWS. THE PATIENT EXPERIENCED A POST-OP DEVICE MALFUNCTION. PATIENT HAD EVENT SUCH AS INFECTION, NON-UNION, ALLERGIC REACTION, OSTEOPOROSIS, OVERLOADING, PAIN, DEGENERATIVE DISEASES, BLEEDING OR OOZING. THERE WAS REVISION SURGERY. DEVICE WAS EXPLANTED DUE TO MAL REDUCTION. PATIENT EXPERIENCED CLINICAL OUTCOME SUCH AS INFECTION AND INFLAMMATION. THERE WAS OTHER MEDICAL INTERVENTION ( X-RAYS, ADDITIONAL PROCEDURES, PRESCRIPTIONS, OTC, REVISION). REVISION TO RADIAL HEAD REPLACEMENT. CONCOMITANT DEVICE REPORTED (UNK - SCREWS: CORTEX PART# UNKNOWN; LOT# UNKNOWN; QUANTITY: UNKNOWN). THIS REPORT IS FOR ONE (1) 2.4 LCP RADIAL HEAD RIM PL 3 HOLES-LFT. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 14939602 ↗
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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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