PlainRecalls
FDA Devices Moderate Class II Ongoing

NEO DELTA SELFSAFE PUR T, I.V. Catheter: a) REF 3738522 b) REF 3738822

Reported: August 25, 2021 Initiated: June 21, 2021 #Z-2303-2021

Product Description

NEO DELTA SELFSAFE PUR T, I.V. Catheter: a) REF 3738522 b) REF 3738822

Reason for Recall

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

Details

Recalling Firm
Delta Med SpA
Units Affected
14,000 units
Distribution
US Nationwide distribution in the states of FL and MN.
Location
Viadana, N/A

Frequently Asked Questions

What product was recalled?
NEO DELTA SELFSAFE PUR T, I.V. Catheter: a) REF 3738522 b) REF 3738822. Recalled by Delta Med SpA. Units affected: 14,000 units.
Why was this product recalled?
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Which agency issued this recall?
This recall was issued by the FDA Devices on August 25, 2021. Severity: Moderate. Recall number: Z-2303-2021.