BD Bactec Blood Culture Procedural Tray, Cat. Number 442805 Becton, Dickinson and Company, 7 Loveton Circle, Sparks, MD
FDA device recall Z-3029-2011 · posted 2011-08-16 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- BD Vacutainer Push Button Blood Collection Set can potentially undergo cannula separation from the hub.
- Action taken
- BD Diagnostics sent a "Lot Specific Product Recall" letter dated April 22, 2011 to all affected customers. The letter asked customers return any affected product and provides instructions for its return. The letter ask customers return the attached Packaging List with the shipment. For question on this recall contact BD Diagnostics at (201) 847-5117.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- JGE
- Quantity affected
- 34960 units
- Distribution
- Nationwide (USA) Distribution.
- Date initiated
- 2011-04-22
- Date posted
- 2011-08-16
- Date terminated
- 2012-06-06
- Location
- Franklin Lakes, NJ
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