Z-2303-2021 Class II Ongoing

Recalled by Delta Med SpA — Viadana, N/A

FDA device recall Z-2303-2021 was initiated by Delta Med SpA on June 21, 2021 and is designated Class II. Reason for recall: Problems related to the sterilization of the medical devices; possible missing sterility of the medical device The recall status is ongoing. Affected quantity: 14,000 units.

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
14,000 units

Product Description

NEO DELTA SELFSAFE PUR T, I.V. Catheter: a) REF 3738522 b) REF 3738822

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

a) REF 3738522, Lot 00A2160813 b) REF 3738822, Lot 00A1160822