Delta Med SpA Via Guido Rossa 20 Viadana Italy DELTAVEN Y, Safety I.V. Catheter in Pur with closed system a) REF 3832072 b) REF 3810072 c) REF 3842072 d) REF 3852072 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DELTAVEN Y, Safety I.V. Catheter in Pur with closed system a) REF 3832072 b) REF 3810072 c) REF 3842072 d) REF 3852072
Brand
Delta Med SpA Via Guido Rossa 20 Viadana Italy
Lot Codes / Batch Numbers
a) REF 3832072, Lot 11T80190 b) REF 3810072, Lot 11T80303 c) REF 3842072, Lot 12T80342 d) REF 3852072, Lot 12T80348
Products Sold
a) REF 3832072, Lot 11T80190 b) REF 3810072, Lot 11T80303 c) REF 3842072, Lot 12T80342 d) REF 3852072, Lot 12T80348
Delta Med SpA Via Guido Rossa 20 Viadana Italy is recalling DELTAVEN Y, Safety I.V. Catheter in Pur with closed system a) REF 3832072 b) REF 3810072 c) REF 3842 due to Problems related to the sterilization of the medical devices; possible missing sterility of the medical device. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Recommended Action
Per FDA guidance
The firm disseminated the notices on 06/21/2021 by email. The firm is requesting destruction of the affected devices at the consignee.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026