RegWardenFDA facility compliance records
Facility

MOZARC MEDICAL US LLC

3 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2025: 2 recalls; 2026: 1 recalls201720182019202020212022202320242202512026
  • Recalls (3)

Devices registered here (1)

  • Catheter, Peritoneal, Long-Term Indwelling
    Product code FJS (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.5630

Recalls & enforcement

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “MOZARC MEDICAL US LLC (FEI 3030574705) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3030574705-mozarc-medical-us-llc/

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