Recall Z-0179-2022— Becton Dickinson & Company
Class II · Terminated
Class II FDA medical device recall by Becton Dickinson & Company, initiated 2021-09-27, terminated 2023-05-04. FDA's recall record names no specific 510(k) clearance for this event. Product: BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf carton. Used to seal syringes and maintain container closure integrity throughout the shelf life of the BD WWD syringe. Catalog Number: 305822. Reason: Holes in product packaging impacts package integrity and may compromise sterility..
- Recalling firm
- Becton Dickinson & Company
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-09-27
- Terminated
- 2023-05-04
- Firm location
- Franklin Lakes, NJ, United States
Product description
BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf carton. Used to seal syringes and maintain container closure integrity throughout the shelf life of the BD WWD syringe. Catalog Number: 305822
Reason for recall
Holes in product packaging impacts package integrity and may compromise sterility.
Data sourced from openFDA. This site is unofficial and independent of the FDA.