GLIDESHEATH SLENDERRecalls & reported problems across all models
Terumo Medical Corporation · 13 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one GLIDESHEATH SLENDER model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 401
- Deaths reported
- 0
- Injuries reported
- 56
- Recalls
- 1
We found 13 models of GLIDESHEATH SLENDER by Terumo Medical Corporation in the FDA's device registry (GUDID). Together they are named in 401 adverse event reports in the FDA's MAUDE database, received between Mar 23, 2017 and Aug 13, 2026 — classified as 56 injuries, 345 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (113 reports).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
GLIDESHEATH SLENDER recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Jun 15, 2026Class IIOpen, Classified
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
Z-2930-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported GLIDESHEATH SLENDER problems
Device problems
- Leak/Splash113
- Material Deformation67
- Product Quality Problem53
- Difficult to Insert40
- Break31
- Difficult to Advance29
- Material Separation18
- Physical Resistance/Sticking14
Patient problems
- No Clinical Signs, Symptoms or Conditions189
- No Consequences Or Impact To Patient101
- Blood Loss76
- Foreign Body In Patient12
- Insufficient Information10
- Hematoma6
- Hemorrhage/Blood Loss/Bleeding4
- No Information4
GLIDESHEATH SLENDER models
13 models, most reported first. Each model has its own page with its reports, recalls and device details.
- GLIDESHEATH SLENDER 80-1060INTRODUCER, CATHETER192 reports
- GLIDESHEATH SLENDER 60-1060INTRODUCER, CATHETER1 recall107 reports
- GLIDESHEATH SLENDER 80-1050INTRODUCER, CATHETER30 reports
- GLIDESHEATH SLENDER 50-1050INTRODUCER, CATHETER25 reports
- GLIDESHEATH SLENDER 50-1060INTRODUCER, CATHETER24 reports
- GLIDESHEATH SLENDER 60-1065INTRODUCER, CATHETER5 reports
- GLIDESHEATH SLENDER 80-1065INTRODUCER, CATHETER4 reports
- GLIDESHEATH SLENDER 80-1660INTRODUCER, CATHETER4 reports
- GLIDESHEATH SLENDER 60-1050INTRODUCER, CATHETER3 reports
- GLIDESHEATH SLENDER 50-1070INTRODUCER, CATHETER2 reports
- GLIDESHEATH SLENDER 80-1055INTRODUCER, CATHETER2 reports
- GLIDESHEATH SLENDER 80-1070INTRODUCER, CATHETER2 reports
- GLIDESHEATH SLENDER 80-1670INTRODUCER, CATHETER1 report
Recent GLIDESHEATH SLENDER adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionAug 13, 2026Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50243745 ↗MalfunctionJul 17, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25857629 ↗MalfunctionJul 17, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25855962 ↗MalfunctionJul 17, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25855960 ↗MalfunctionJul 17, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25855948 ↗MalfunctionJul 13, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25796468 ↗MalfunctionJul 12, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25791687 ↗MalfunctionJul 12, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25791686 ↗MalfunctionJul 12, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25791684 ↗MalfunctionJul 12, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25791671 ↗MalfunctionJul 12, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25791670 ↗MalfunctionJul 12, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25791668 ↗MalfunctionJul 12, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25791427 ↗MalfunctionJul 12, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25791426 ↗MalfunctionJul 10, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25781911 ↗
Other Terumo Medical Corporation products
All Terumo Medical Corporation devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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