ACUMED 80-1635Recalls & reported problems
Acumed LLC · Polarus® 3 Cap Screw Driver · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10806378050527), received between Jan 9, 2026 and Jan 9, 2026 — classified as 2 malfunctions.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 9, 2026Adverse Event Without Identified Device or Use Problem
THE DISTRIBUTOR REPORTED THAT "DURING THE POLARUS 3 SURGERY, IT SEEMS HE HAD SOME DIFFICULTY INSERTING THE CAP SCREW." NO ADVERSE EFFECT, BUT A DELAY OF 20 MINUTES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24024436 ↗MalfunctionJan 9, 2026Adverse Event Without Identified Device or Use Problem
THE DISTRIBUTOR REPORTED THAT "DURING THE POLARUS 3 SURGERY, IT SEEMS HE HAD SOME DIFFICULTY INSERTING THE CAP SCREW." NO ADVERSE EFFECT, BUT A DELAY OF 30 MINUTES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24024434 ↗
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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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