Class II

Medical Device Recall: Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.

Mozarc Medical US LLC · April 23, 2025

Reason for Recall

Potential breach of sterile barrier packaging.

Distribution

Worldwide distribution - US Nationwide and the countries of Canada & Mexico.

States Affected

NATIONWIDE

Quantity Affected

95,938 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1886-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Mozarc Medical US LLC Medical Device Recall: Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter. | SafeCheck