Peripheral Catheter Insertion Kit ST220081Recalls & reported problems
Bard Access Systems, Inc. · Sldgr IDC, 20gx8cm, Full w/o Guardiva · Class 2
All models of Peripheral Catheter Insertion Kit (54)
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 00801741139314), received between Oct 8, 2019 and Jul 23, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (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. 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
- Material Deformation2
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 23, 2024Material Deformation; Material Deformation
IT WAS REPORTED BY CUSTOMER THAT THE POWERGLIDE ST KINKING DIRECTLY AFTER INSERTION, LINE WON'T ASPIRATE, REMOVED CATHETER AND VISIBLE CATHETER KINKING. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19807144 ↗MalfunctionOct 8, 2019Material Deformation; Material Deformation
IT WAS REPORTED THAT OVER THE WIRE POWERGLIDE WAS INSERTED ON PATIENT IN RIGHT UPPER ARM IN THE ER. CATHETER KINKED BEFORE LEAVING THE PATIENT'S BEDSIDE. UNABLE TO WITHDRAWAL BLOOD. HAD TO REINSERT DIFFERENT TYPE OF MIDLINE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9169969 ↗
Other Midline catheter devices
- Midline Catheter Kit P4154108DBard Access Systems, Inc. · Midline catheter1 recall1 death126 reports
- ARROW IPN921959Teleflex Incorporated · Midline catheter2 recalls0 reports
- Midline Catheter Kit S4153108BDPBard Access Systems, Inc. · Midline catheter1 recall36 reports
- Midline Catheter Kit S4153108DBard Access Systems, Inc. · Midline catheter1 recall32 reports
- Midline Catheter Kit S4153108DGPBard Access Systems, Inc. · Midline catheter1 recall15 reports
- Midline Catheter Kit S4254108BDPBard Access Systems, Inc. · Midline catheter1 recall11 reports
- Midline Catheter Kit P4154108Bard Access Systems, Inc. · Midline catheter1 recall10 reports
- ARROW IPN037698Teleflex Incorporated · Midline catheter1 recall9 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 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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