FDAFDA · Food and drugs·Recall number Z-0081-2020
Cap Change Kit DT20310
Published October 16, 2019 · Recall initiated: April 24, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Centurion Medical Products Corporation
- Distributor
- Nationwide domestic distribution.
- Lot
- 2017032780 2017052280 2017070380 2017072480 2017091180
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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