FDAFDA · Food and drugs·Recall number Z-0082-2020
Neonatal Cap Change Kit DT20315
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
- 2017042480 2017061980 2017082880
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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