Palindrome 8888145063PRecalls & reported problems
Mozarc Medical US LLC · Precision SI Chronic Catheter Kit,Symmetrical Tip, Silver Ion Sleeve and Tal VenaTrac Stylet,14.5 Fr/Ch (4.8 mm) x 23 cm · Class 2 · Implant
All models of Palindrome (133)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521158351), received between Aug 11, 2021 and Aug 11, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Deformation” (1 report).
49 other recalls cover devices cleared under the same FDA submission (K123196); they may or may not involve this specific model.
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.
Most reported problems
Device problems
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 11, 2021Material Deformation; Material Deformation
ACCORDING TO THE REPORTER, THERE WERE BUBBLES NOTED ON THE SILVER ION SLEEVE OF THE CATHETER WHEN IT WAS REMOVED FROM THE PATIENT. IT WAS ALSO STATED THAT BLOOD TRANSFUSION WAS NOT REQUIRED, THERE WAS NO INTERVENTION/TREATMENT REQUIRED AS THE RESULT OF THE EVENT, NOTHING UNUSUAL WAS OBSERVED ON THE DEVICE PRIOR TO USE, THERE WAS NO OTHER PRODUCT UTILIZED WITH THE DEVICE AND THERE WAS NO VISIBLE DEFECTS NOTED WHEN THE CATHETER WAS INITIAL INSERTED. THE CATHETER WAS NOT REPAIRED, THERE WAS NO LUER ADAPTER ISSUE AND THERE WAS NO MEDICAL INTERVENTION DONE TO THE PATIENT. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12308603 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K123196. One submission often covers many models, so check the product and lot details in each record.
- Z-1888-2025 · Apr 23, 2025 · Open, ClassifiedPalindrome Precision H Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
- Z-1887-2025 · Apr 23, 2025 · Open, ClassifiedPalindrome Precision SI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
- Z-1889-2025 · Apr 23, 2025 · Open, ClassifiedMAHURKAR Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
- Z-1886-2025 · Apr 23, 2025 · Open, ClassifiedPalindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
- Z-1885-2025 · Apr 23, 2025 · Open, ClassifiedPalindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
- Z-1634-2024 · Mar 15, 2024 · Open, ClassifiedPalindrome Precision HSI Chronic Catheter Sport Pack 14.5 Fr/Ch (4.8mm) x 19 cm (Symmetrical Tip, Heparin Coating, Silver Ion Sleeve and Tal VenaTrac Stylet- Intended for acute a
- Z-1635-2024 · Mar 15, 2024 · Open, ClassifiedPalindrome Precision H Chronic Catheter Kit 14.5 Fr/Ch (4.8mm) x 23 cm (Symmetrical Tip, Heparin Coating and Tal VenaTrac Stylet- Intended for acute and chronic hemodialysis, aph
- Z-1314-2022 · Jun 8, 2022 · Open, ClassifiedPalindrome Precision SI Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
- Z-1313-2022 · Jun 8, 2022 · Open, ClassifiedPalindrome Precision H Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
- Z-1315-2022 · Jun 8, 2022 · Open, ClassifiedPalindrome Precision HSI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
- Z-1312-2022 · Jun 8, 2022 · Open, ClassifiedPalindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
- Z-2371-2021 · May 28, 2021 · Open, ClassifiedPalindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 23 cm, Item Code 8888541023P
- Z-2372-2021 · May 28, 2021 · Open, ClassifiedPalindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 28 cm, Item Code 8888541028P
- Z-2373-2021 · May 28, 2021 · Open, ClassifiedPalindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 33 cm, Item Code 8888541033P
- Z-2375-2021 · May 28, 2021 · Open, ClassifiedPalindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 55 cm, Item Code 8888541055P
…and 34 more.
Other Catheter, hemodialysis, implanted devices
- Palindrome 8888145014Mozarc Medical US LLC · Catheter, hemodialysis, implanted1 recall312 reports
- Palindrome 8888145015Mozarc Medical US LLC · Catheter, hemodialysis, implanted2 recalls1 death219 reports
- HemoStar Long-Term Hemodialysis Catheter 5833690Bard Access Systems, Inc. · Catheter, hemodialysis, implanted2 deaths290 reports
- Palindrome 8888119369PMozarc Medical US LLC · Catheter, hemodialysis, implanted3 recalls1 death14 reports
- HemoStar Long-Term Hemodialysis Catheter 5833730Bard Access Systems, Inc. · Catheter, hemodialysis, implanted1 death141 reports
- GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet 5393230Bard Access Systems, Inc. · Catheter, hemodialysis, implanted5 deaths138 reports
- Palindrome 8888123404PMozarc Medical US LLC · Catheter, hemodialysis, implanted2 recalls1 death17 reports
- Palindrome 8888119364PMozarc Medical US LLC · Catheter, hemodialysis, implanted2 recalls1 death17 reports
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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