Reported Aug 25, 2021 · Ongoing

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

Delta Med SpA

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Delta Med SpA · Via Guido Rossa 20 · Viadana, N/A · N/A

Is this the product you have?

  • DELTAVEN Y DNL Safety I.V
  • Catheter in Pur with closed systema) REF 3832572 b) REF 3842572 c) REF 3821572 d) REF 3833572 e) REF 3831572 f) REF 3810572 g) REF 3852572
Lot codes and dates
  • a) REF 3832572
    • Lot 11T80189 b) REF 3842572
    • Lot 11T80198 c) REF 3821572
    • Lot 11T80149 d) REF 3833572
    • Lot 11T80292 e) REF 3831572
    • Lot 12T80230 f) REF 3810572
    • Lot 12T80302 g) REF 3852572
    • Lot 12T80349
Amount recalled
203,680 units

This recall covers 11 products

The agency filed one notice per product. You are reading one of them; the other 10 are below.

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Delta Med SpA recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:35 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.