PlainRecalls
FDA Devices Moderate Class II Ongoing

NEO DELTA Self Safe, I.V. Catheter REF 3738222

Reported: August 25, 2021 Initiated: June 21, 2021 #Z-2299-2021

Product Description

NEO DELTA Self Safe, I.V. Catheter REF 3738222

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
10,000 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 Self Safe, I.V. Catheter REF 3738222. Recalled by Delta Med SpA. Units affected: 10,000 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-2299-2021.