Medline DYNSCS22100Recalls & reported problems
Medline Industries, Inc. · CATHETER,IV,SURESITE SLIDE,22G X 1" · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10888277667549), received between Sep 10, 2019 and Sep 28, 2026 — classified as 2 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Dull, Blunt” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Dull, Blunt2
- Break1
- Fail-Safe Did Not Operate1
- Fail-Safe Problem1
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Foreign Body In Patient1
- Needle Stick/Puncture1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Dull, Blunt; Fail-Safe Problem
It was reported that "they are not sharp enough, and the safety feature does not always work."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50915278 ↗MalfunctionJun 9, 2026Fail-Safe Did Not Operate
CUSTOMER PROVIDED THE DESCRIPTION THAT "THE SAFETY FEATURE DOES NOT ALWAYS WORK". CUSTOMER PROVIDED MULTIPLE GAUGE SIZES AND LOT NUMBERS AS POSSIBLY AFFECTED. THE PART NUMBERS AND LOT NUMBERS PROVIDED ARE AS FOLLOWS: DYNSCS22100 - LOT: 27825060001 DYNSCS20100 - LOT: 27824100001 DYNSCS20100 - LOT: 27825010001 DYNSCS20100 - LOT: 27825060005. DYNSCS24340 - LOT: 27825060002. DYNSCS24340 - LOT: 27825010002.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25449210 ↗InjurySep 17, 2025Break; Break
ACCORDING TO THE CUSTOMER, ON (B)(6) 2025 LEAKING WAS OBSERVED FROM THE LEFT ANTECUBITAL FOSSA IV SITE PRIOR TO TRANSFER TO PACU AND IT WAS DISCOVERED THAT THE "TIP OF THE CATHETER HAD DISCONNECTED FROM THE HUB OF THE IV."
Patient problems: Foreign Body In Patient; No Clinical Signs, Symptoms or Conditions
MAUDE report 23073958 ↗InjuryApr 3, 2024Material Integrity Problem; Material Integrity Problem
MalfunctionSep 10, 2019Dull, Blunt
IT WAS REPORTED THAT THE IV CATHETERS WERE DULL AND THAT AN UNKNOWN NUMBER OF PATIENTS REQUIRED ADDITIONAL IV STICKS.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8982623 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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