Integra® 3722110Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Paparella Sickle Knife, Straight, 5mm Blade · Class 1
Data updated Oct 13, 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 10381780082217), received between Aug 30, 2022 and Aug 30, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Packaging Problem” (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.
Most reported problems
Device problems
- Packaging Problem1
Patient problems
- Laceration(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 30, 2022Packaging Problem; Packaging Problem
A FACILITY REPORTED THAT THE CUSTOMER WAS CUT BY THE SICKLE KNIFE (3722110) WHEN OPENING THE BOX. IT WAS REPORTED THE INSTRUMENT WAS NOT IN ANY PACKAGING; THERE WAS NO PROTECTIVE COVERING OR BUBBLE WRAP. THERE WAS NO PATIENT INVOLVEMENT; THUS, NO PATIENT INJURY OR SURGICAL DELAY WAS REPORTED.
Patient problems: Laceration(s)
MAUDE report 15324608 ↗
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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