Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2301-2021 — NEO DELTA Self Safe T, I.V. catheter of PUR a) REF 3779422 b) REF 3769522 c) REF 3708522

U.S. FDA — Device Enforcement · Italy · 2021-06-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2301-2021
Date of alert
2021-06-21
Country / jurisdiction
Italy
Risk level
Class II
Risk type
recall
Brand
Delta Med SpA
Product category
device
Product type
Devices
Reported risk: Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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