FDA Enforcement
Class II
Terminated
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
Recall: Z-0499-2020
·
Reported November 27, 2019
Enforcement
- Recall Number
- Z-0499-2020
- Event ID
- 84113
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Becton Dickinson & Company
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- November 27, 2019
- Initiation Date
- October 14, 2019
- Classification Date
- November 20, 2019
- Termination Date
- October 16, 2020
- Address
- 1 Becton Dr, N/A, Franklin Lakes, NJ, 07417-1815, United States
Description
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
Reason
Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
Code Info
Lot Number: 9142881 UDI: 50382903065474
Distribution
Distribution US Nationwide and Canada
Quantity
1,632,000