Medical device recalls Moderate risk

Delta Med SpA recalls DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed system: a) REF 3832572 b) REF 3842572 c) REF 3821572 d) REF 3833…

Recall date
June 21, 2021
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2296-2021
FDA classification
Class II
Brand / firm
Delta Med SpA
Sold / distributed
US Nationwide distribution in the states of FL and MN.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed system: a) REF 3832572 b) REF 3842572 c) REF 3821572 d) REF 3833572 e) REF 3831572 f) REF 3810572 g) REF 3852572

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