NA 0747031650Recalls & reported problems
Stryker Corporation · Inflow/Outflow Cannula, 2 Rotating Stopcocks · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327054613), received between May 20, 2020 and May 20, 2020 — classified as 2 injuries.
The most frequently reported specific device problem is “Contamination of Device Ingredient or Reagent” (2 reports).
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
- Contamination of Device Ingredient or Reagent2
- Adverse Event Without Identified Device or Use Problem1
- Contamination /Decontamination Problem1
Patient problems
- Device Embedded In Tissue or Plaque2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 20, 2020Contamination of Device Ingredient or Reagent; Contamination of Device Ingredient or Reagent; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT DEBRIS REMAINED INSIDE THE PATIENT.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 10076895 ↗InjuryMay 20, 2020Contamination /Decontamination Problem; Contamination of Device Ingredient or Reagent; Contamination /Decontamination Problem; Contamination of Device Ingredient or Reagent
IT WAS REPORTED THAT DEBRIS REMAINED INSIDE THE PATIENT.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 10076876 ↗
Other TRAY, SURGICAL, INSTRUMENT devices
- PINNACLE 2220-00-100Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT74 reports
- ACTIS 2010-04-200Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT66 reports
- ATTUNE 2545-01-703Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT62 reports
- ATTUNE 2545-01-704Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT57 reports
- INSTRUMENT 6541-9-109Howmedica Osteonics Corp. · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- Medical Action Industries 6805Medical Action Industries Inc. · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- n.a. 39501CECKarl Storz GmbH & Co. KG · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- n.a. 11580AKarl Storz GmbH & Co. KG · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
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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