DRI-LOK 3910090800Recalls & reported problems
Stryker Corporation · [Threaded Cannula. Do not resterilize, Do not use if package is damaged] · Class 1
All models of DRI-LOK (3)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327055795), received between Oct 5, 2021 and Oct 5, 2021 — classified as 3 injuries.
The most frequently reported specific device problem is “Leak/Splash” (3 reports).
1 FDA recall record name this device's identifier.
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 18, 2026.
Recalls naming this device
- Dec 21, 2017Class IICompleted
Inadvertent shipment of expired units.
Z-2057-2018 · Root cause: Incorrect or no expiration date · Recall details · FDA record ↗
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem3
- Leak/Splash3
Patient problems
- Extravasation3
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 5, 2021Leak/Splash; Leak/Splash; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT EXPERIENCED EXTRAVASATION.
Patient problems: Extravasation; No Clinical Signs, Symptoms or Conditions
MAUDE report 12578304 ↗InjuryOct 5, 2021Leak/Splash; Leak/Splash; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT EXPERIENCED EXTRAVASATION.
Patient problems: Extravasation; No Clinical Signs, Symptoms or Conditions
MAUDE report 12578303 ↗InjuryOct 5, 2021Leak/Splash; Leak/Splash; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT EXPERIENCED EXTRAVASATION.
Patient problems: Extravasation; No Clinical Signs, Symptoms or Conditions
MAUDE report 12578302 ↗
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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 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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