Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

DELTAVEN Y Recalled by Delta Med SpA Due to Problems related to the sterilization of the medical...

Date: June 21, 2021
Company: Delta Med SpA
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Delta Med SpA directly.

Affected Products

DELTAVEN Y, Safety I.V. Catheter in Pur with closed system a) REF 3832072 b) REF 3810072 c) REF 3842072 d) REF 3852072

Quantity: N/A

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Delta Med SpA

Delta Med SpA has 11 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report