Z-2295-2021 Class II Ongoing

Recalled by Delta Med SpA — Viadana, N/A

FDA device recall Z-2295-2021 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: 30,900 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
30,900 units

Product Description

DELTAVEN Safety I.V. Catheter in Pur with closed system: a) REF 3836272 b) REF 3814272 c) REF 3845272 d) REF 3856272

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 3836272, Lot 11T80188 b) REF 3814272, Lot 11T80272 c) REF 3845272, Lot 12T80147 d) REF 3856272, Lot 12T80347