Grip-Lok 3300M-10PKRecalls & reported problems
Tidi Products, LLC · Grip-Lok Universal Securement Device White Loop/Liner/Hook/Bandage/Liner Sterile Medium 10 per Package · Class 1
All models of Grip-Lok (11)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00618125134717), received between Jul 22, 2024 and Dec 26, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (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
- Loss of or Failure to Bond2
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 26, 2024Loss of or Failure to Bond; Loss of or Failure to Bond
AMAZON REVIEW: I BOUGHT THESE TO HOLD MY CATH TUBING IN PLACE, SPENT OVER $(B)(6) FOR 10 OF THEM AND THEY DON'T WORK, WITHIN AN HOUR IT WASN'T STUCK TO MY SKIN ANYMORE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21020198 ↗MalfunctionDec 26, 2024Loss of or Failure to Bond; Loss of or Failure to Bond
AMAZON REVIEW: THIS EXPENSIVE CATHETER STABILIZATION DEVICE COMES LOOSE AFTER A FEW DAYS. IT IS VERY DIFFICULT TO REMOVE THE CATHETER FROM THE DEVICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21020188 ↗MalfunctionJul 22, 2024Mechanical Problem; Mechanical Problem
AMAZON REVIEW: THE LAST 2 TIMES I'VE ORDERED THESE FOR MY SON THEY HAVE ALL BEEN BAD. WE NORMALLY GET 3 TO 5 DAYS EVEN WITH BATHING OR SWIMMING. WE GET ABOUT A MONTH FROM 1 ORDER. I'VE HAD TO USE 5 IN 9 DAYS AS THEY BARELY STICK TO HIS SKIN AND THE VELCRO BARELY HOLDS HIS TUBE. IF THE NEXT BATCH IS BAD I'M GOING ELSEWHERE. WASTED MONEY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19796514 ↗
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- Grip-Lok 3601CVCTidi Products, LLC · Device, Intravascular Catheter Securement12 reports
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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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