FDA Enforcement Class II Ongoing

DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed system: a) REF 3832572 b) REF 3842572 c) REF 3821572 d) REF 3833572 e) REF 3831572 f) REF 3810572 g) REF 3852572

Recall: Z-2296-2021 · Reported August 25, 2021

Enforcement

Recall Number
Z-2296-2021
Event ID
88234
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Delta Med SpA
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
August 25, 2021
Initiation Date
June 21, 2021
Classification Date
August 16, 2021
Address
Via Guido Rossa 20, N/A, Viadana, N/A, N/A, Italy

Description

DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed system: a) REF 3832572 b) REF 3842572 c) REF 3821572 d) REF 3833572 e) REF 3831572 f) REF 3810572 g) REF 3852572

Reason

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

Code Info

a) REF 3832572: Lot 11T80189 b) REF 3842572, Lot 11T80198 c) REF 3821572, Lot 11T80149 d) REF 3833572, Lot 11T80292 e) REF 3831572, Lot 12T80230 f) REF 3810572, Lot 12T80302 g) REF 3852572, Lot 12T80349

Distribution

US Nationwide distribution in the states of FL and MN.

Quantity

203,680 units