PalindromeRecalls & reported problems across all models
Mozarc Medical US LLC · 133 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Palindrome models — page 2
133 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Palindrome 8888145061Catheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888145046CCatheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888119364Catheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888119371Catheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888128454Catheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888145070Catheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888145050CCatheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888128458PCatheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888133508PCatheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888145050PCatheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888145057CPCatheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888145061PCatheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888145068PCatheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888145069PCatheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888145070PCatheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888145071PCatheter, hemodialysis, implanted1 recall0 reports
- Palindrome 8888541023PCatheter, hemodialysis, implanted1 death32 reports
- Palindrome 8888541028PCatheter, hemodialysis, implanted13 reports
- Palindrome 8888541019PCatheter, hemodialysis, implanted8 reports
- Palindrome 8888541028Catheter, hemodialysis, implanted5 reports
- Palindrome 8888145062PCatheter, hemodialysis, implanted3 reports
- Palindrome 8888541044PCatheter, hemodialysis, implanted3 reports
- Palindrome 8888128455Catheter, hemodialysis, implanted1 report
- Palindrome 8888133504Catheter, hemodialysis, implanted1 report
- Palindrome 8888541033Catheter, hemodialysis, implanted1 report
- Palindrome 8888541055Catheter, hemodialysis, implanted1 report
- Palindrome 8888541123Kit, repair, catheter, hemodialysis1 report
- Palindrome 8888541128Kit, repair, catheter, hemodialysis1 report
- Palindrome 8888145063CPCatheter, hemodialysis, implanted1 report
- Palindrome 8888145063PCatheter, hemodialysis, implanted1 report
- Palindrome 8888145064PCatheter, hemodialysis, implanted1 report
- Palindrome 8888541033PCatheter, hemodialysis, implanted1 report
- Palindrome 8888541055PCatheter, hemodialysis, implanted1 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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