Delta Med SpA Via Guido Rossa 20 Viadana Italy NEO DELTA SELFSAFE PUR T, I.V. Catheter: a) REF 3738522 b) REF 3738822 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
NEO DELTA SELFSAFE PUR T, I.V. Catheter: a) REF 3738522 b) REF 3738822
Brand
Delta Med SpA Via Guido Rossa 20 Viadana Italy
Lot Codes / Batch Numbers
a) REF 3738522, Lot 00A2160813 b) REF 3738822, Lot 00A1160822
Products Sold
a) REF 3738522, Lot 00A2160813 b) REF 3738822, Lot 00A1160822
Delta Med SpA Via Guido Rossa 20 Viadana Italy is recalling NEO DELTA SELFSAFE PUR T, I.V. Catheter: a) REF 3738522 b) REF 3738822 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