Z-2299-2021 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
10,000 units

Product Description

NEO DELTA Self Safe, I.V. Catheter REF 3738222

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 3738222, Lot 00A1160625