Z-2304-2021 Class II Ongoing

Recalled by Delta Med SpA — Viadana, N/A

Recall Details

Product Type
Devices
Report Date
August 25, 2021
Initiation Date
June 21, 2021
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
N/A

Product Description

NEO DELTA SELFSAFE PUR T, I.V. Catheter:

Reason for Recall

Problems related to the sterilization of the medical devices; possible missing sterility of the medical device

Distribution Pattern

US Nationwide distribution in the states of FL and MN.

Code Information

REF 3738522, Lot 00A2160813 REF 3738822, Lot 00A1160822