BASIS 71312263Recalls & reported problems
Smith & Nephew, Inc. · BASIS 12/14 TAPER PRIMARY COLLARED STEM SIZE 3 · Class 2 · Implant
- 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 03596010412928), received between Mar 26, 2024 and Mar 26, 2024 — classified as 1 injury.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 26, 2024Break; Break
IT WAS REPORTED THAT, AFTER A THR HAD BEEN PERFORMED, PATIENT EXPERIENCED PROGRESSIVELY WORSENING PAIN IN RIGHT HIP DUE TO STEM BREAKAGE PROSTHETIC IN ITS MID-DISTAL. THIS WAS OBSERVED DURING X-RAY. THIS ADVERSE EVENT WAS ADDRESSED BY REVISION SURGERY ON (B)(6) 2024, IN WHICH THE BASIS 12/14 TPR PRI CLLD SZ 3 WAS EXCHANGE. PATIENT'S CURRENT HEALTH STATUS IS UNKNOWN.
Patient problems: Failure of Implant
MAUDE report 18977106 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.