MILLENNIUM 0-47130Recalls & reported problems
Avalign Technologies, Inc. · Lewin Bone Forceps · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00190776341381), received between Mar 11, 2026 and Mar 11, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 11, 2026Detachment of Device or Device Component
DURING A MAKO ASSISTED LEFT TOTAL HIP CASE, THE LEWIN CLAMP BROKE. THE SURGEON INSPECTED THE INSTRUMENT AND THE PATIENT; THE SCRUB TECH AND CIRCULATOR INSPECTED THE EQUIPMENT. SPD WAS CONTACTED TO COME AND INSPECT THE INSTRUMENT; ALL PARTIES INVOLVE AGREE THAT ALL PARTS OF THE INSTRUMENT WERE OBTAINED AND ACCOUNTED FOR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24571787 ↗
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- Centurion 66195Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
- Centurion 66440Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.