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[Recalled] CAP CHANGE KIT DYNDC1496B — Firm distributes kits which include the BD MaxZeroNeedleess Connector, which wa… | FDA 2019-04-24

recall fda device united-states

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

ProductCAP CHANGE KIT DYNDC1496B
Brand / manufacturerCenturion Medical Products Corporation
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0083-2020
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date24 April 2019
EAN / barcode2018101590

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Centurion Medical Products Corporation

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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