McKesson 200-IVS221Recalls & reported problems
Mckesson Medical-Surgical Inc. · "Sliding Safety IV Catheter STRAIGH HUB 22G x 1 in (0.9 mm x 25.4 mm)" · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10612479267548), received between Jun 25, 2024 and Apr 7, 2026 — classified as 4 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (4 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. 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
- Detachment of Device or Device Component4
- Material Separation3
Patient problems
- Foreign Body In Patient3
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
- Unspecified Vascular Problem1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryApr 7, 2026Material Separation
THE FLEXIBLE CANNULA BECAME LODGED IN THE PATIENT'S ARM. IT APPEARS THAT IT WAS DETACHED FROM ITS HOUSING OR FROM THE PLASTIC THAT SHOULD HAVE HELD IT IN PLACE SO THAT IT COULD BE REMOVED FROM THE PATIENT'S ARM AT THE END OF THE PROCEDURE. THE PATIENT WAS TRANSFERRED TO THE HOSPITAL FOR FURTHER TREATMENT AND RETRIEVAL.
Patient problems: Foreign Body In Patient
MAUDE report 24809234 ↗MalfunctionApr 7, 2026Material Separation
PLASTIC CLEAR TIP OF THE CATHETER BROKE OFF INSIDE THE PATIENT. AFTER THE INCIDENT, THE NURSE HAD TO APPLY PRESSURE TO MILK THE CATHETER OUT OF THE PATIENT'S VEIN. SHE THEN PROCEEDED TO START ANOTHER IV. THE CATHETER TIP BROKE OFF THE RIDGED CATHETER HUB. NO MEDICAL TREATMENT WAS NECESSARY.
Patient problems: Foreign Body In Patient
MAUDE report 24809233 ↗InjuryMar 12, 2026Detachment of Device or Device Component
IT WAS REPORTED BY THE CUSTOMER THAT THE FLEXIBLE CANNULA BECAME LODGED IN THE PATIENT'S ARM. THE PATIENT WAS TRANSFERRED TO THE HOSPITAL FOR FURTHER TREATMENT AND RETRIEVAL.
Patient problems: Insufficient Information
MAUDE report 24578871 ↗MalfunctionMar 9, 2026Detachment of Device or Device Component
IT WAS REPORTED BY THE CUSTOMER THAT THE PLASTIC CLEAR TIP OF THE CATHETER BROKE OFF INSIDE THE PATIENT. AFTER THE INCIDENT, THE NURSE HAD TO APPLY PRESSURE TO PUSH THE CATHETER OUT OF THE PATIENT'S VEIN. NO OTHER INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS PRODUCT ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24547472 ↗MalfunctionAug 6, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED BY THE CUSTOMER THAT THE CATHETER BROKE OFF WHILE INSIDE THE PATIENT VEIN. THE PATIENT WAS SENT TO THE HOSPITAL FOR EVALUATION. THE CATHETER WAS ABLE TO BE REMOVED WITHOUT SURGERY. NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS PRODUCT ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22727263 ↗InjuryJun 17, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED BY THE CUSTOMER THAT A PATIENT WAS ADMINISTERED THE IV CATHETER, BUT UPON REMOVAL, IT WAS DISCOVERED THAT THE END PLASTIC CATHETER SHEATH HAD DETACHED FROM THE HUB. IT WAS CONFIRMED THAT THE CATHETER REMAINED LODGED IN THE PATIENT'S ARM. VASCULAR SURGICAL INTERVENTION WAS REQUIRED TO REMOVE IT.
Patient problems: Unspecified Vascular Problem
MAUDE report 22229406 ↗InjuryJun 25, 2024Material Separation; Material Separation
WE HAD A PATIENT WHO WE WERE STARTING AN IV ON IN THE PRE-OP SETTING GETTING A ROUTINE IV. DURING THE IV START THE RN NOTED BLOOD FLOW LEAKAGE WHEN THE CATHETER WAS ADVANCED INTO THE VEIN. SHE THEN WITHDREW THE NEEDLE AND CLEAR SAFETY HOUSING FROM THE HUB. THIS IS WHEN IT WAS NOTED THAT THE PLASTIC TIP WAS NOT PRESENT ON THE BLUE HUB GOING INTO THE PATIENTS SKIN. THE PHYSICIAN'S ASSESSED THE HAND AND DID STATE THAT THEY COULD PALPATE THE PLASTIC CATHETER UNDER THE PATIENT'S SKIN AND FELT IT WAS IN THE VEIN. PRESSURE DRESSING WAS PLACED ABOVE THE SITE AND THE AREA WAS MARKED. THE PATIENT WAS SENT TO FLOWER HOSPITAL FOR REMOVAL OF FOREIGN OBJECT. PATIENT HAD AN AREA WHERE THE CATHETER FELT TO BE PRESENT RIGHT BY INSERTION SITE OF IV START AND PRESSURE DRESSING WAS APPLIED ABOVE SITE TO PREVENT MIGRATION. IT WAS ALSO MARKED. IT WAS CONFIRMED VIA ULTRASOUND AT FLOWER HOSPITAL THAT CATHETER IS PRESENT IN PATIENTS LEFT HAND AND PLASTIC SURGERY HAS BEEN CONSULTED FOR REMOVAL.
Patient problems: Foreign Body In Patient
MAUDE report 19607268 ↗
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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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