TransPort CAT00224Recalls & reported problems
Stryker Corporation · TRANSPORT CANNULA 8MM LENGTH 7, 8, 9 · 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 07613252632849), received between May 9, 2022 and Jul 31, 2024 — classified as 2 malfunctions.
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. 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
- Break1
- Fracture1
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 31, 2024Fracture; Fracture
IT WAS REPORTED THAT A SMALL PIECE OF A PLASTIC CANNULA BROKE OFF DURING THE CASE. WE ARE UNSURE IF THE PIECE BROKE OFF INSIDE THE PATIENT OR OUTSIDE AS THE PIECE WAS NOT RECOVERED. THERE IS NO CERTAINTY ON WHETHER OR NOT THE PIECE WAS LEFT INSIDE THE PATIENT OR NOT. THERE HAS BEEN NO PIECE RECOVERED.
Patient problems: Foreign Body In Patient
MAUDE report 19879187 ↗MalfunctionMay 9, 2022Break
IT WAS REPORTED THAT THE DEVICE BROKE DURING THE PROCEDURE. THE PIECE WAS RETRIEVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14342901 ↗
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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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