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