Z-0102-2020 Class II Terminated
FDA device recall Z-0102-2020 was initiated by Centurion Medical Products Corporation on April 24, 2019 and is designated Class II. Reason for recall: 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 conne… The recall status is terminated (terminated April 3, 2020). Affected quantity: 181965 total.
Recall Details
- Product Type
- Devices
- Report Date
- October 16, 2019
- Initiation Date
- April 24, 2019
- Termination Date
- April 3, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 181965 total
Product Description
IV START KIT IV8440
Reason for Recall
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.
Distribution Pattern
Nationwide domestic distribution.
Code Information
2017061980 2017071780 2017091180 2017102380 2017121880 2018012280 2018022680 2018041680 2018070980