Delta Med SpA: Medical Device Recall in 2021 - (Recall #: Z-2303-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 21, 2021

Date Posted: August 25, 2021

Recall Number: Z-2303-2021

Event ID: 88234

Reason for Recall:

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

Status: Ongoing

Product Quantity: 14,000 units

Code Information:

a) REF 3738522, Lot 00A2160813 b) REF 3738822, Lot 00A1160822

Distribution Pattern:

US Nationwide distribution in the states of FL and MN.

Voluntary or Mandated:

Voluntary: Firm initiated