FlexorRecalls & reported problems across all models
Cook Incorporated · 134 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Flexor models — page 2
134 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Flexor G49046INTRODUCER, CATHETER3 reports
- Flexor G49481INTRODUCER, CATHETER3 reports
- Flexor G56227INTRODUCER, CATHETER3 reports
- Flexor G07465INTRODUCER, CATHETER2 reports
- Flexor G07856INTRODUCER, CATHETER2 reports
- Flexor G11617INTRODUCER, CATHETER2 reports
- Flexor G13212INTRODUCER, CATHETER2 reports
- Flexor G19172endoscopic access overtube, gastroenterology-urology2 reports
- Flexor G30003INTRODUCER, CATHETER2 reports
- Flexor G30120INTRODUCER, CATHETER2 reports
- Flexor G32225INTRODUCER, CATHETER2 reports
- Flexor G35600INTRODUCER, CATHETER2 reports
- Flexor G48188INTRODUCER, CATHETER2 reports
- Flexor G48191INTRODUCER, CATHETER2 reports
- Flexor G56225INTRODUCER, CATHETER2 reports
- Flexor G56234INTRODUCER, CATHETER2 reports
- Flexor G56235INTRODUCER, CATHETER2 reports
- Flexor G07857INTRODUCER, CATHETER1 report
- Flexor G08273INTRODUCER, CATHETER1 report
- Flexor G08681INTRODUCER, CATHETER1 report
- Flexor G08969INTRODUCER, CATHETER1 report
- Flexor G09994INTRODUCER, CATHETER1 report
- Flexor G10405INTRODUCER, CATHETER1 report
- Flexor G10406INTRODUCER, CATHETER1 report
- Flexor G10882INTRODUCER, CATHETER1 report
- Flexor G11211INTRODUCER, CATHETER1 report
- Flexor G19175endoscopic access overtube, gastroenterology-urology1 report
- Flexor G30390endoscopic access overtube, gastroenterology-urology1 report
- Flexor G31133INTRODUCER, CATHETER1 report
- Flexor G35601INTRODUCER, CATHETER1 report
- Flexor G35608INTRODUCER, CATHETER1 report
- Flexor G48190INTRODUCER, CATHETER1 report
- Flexor G48193INTRODUCER, CATHETER1 report
- Flexor G56229INTRODUCER, CATHETER1 report
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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