Becton Dickinson & Company BD 10 ml Syringe Luer Lok Tip, Reorder #3039605, BD, Franklin Lakes, NJ 07417. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BD 10 ml Syringe Luer Lok Tip, Reorder #3039605, BD, Franklin Lakes, NJ 07417.
Brand
Becton Dickinson & Company
Lot Codes / Batch Numbers
Reorder number: 3039605, Lot numbers 7061015, 7061014, 7092726, 7094789, 7094790, 7123223, 7123225, 7150947, 7150949, 7184442, 7184443, 7184446, 7212935, 7239568, 7239570, 7239569, 7271873.
Products Sold
Reorder number: 3039605; Lot numbers 7061015, 7061014, 7092726, 7094789, 7094790, 7123223, 7123225, 7150947, 7150949, 7184442, 7184443, 7184446, 7212935, 7239568, 7239570, 7239569, 7271873.
Becton Dickinson & Company is recalling BD 10 ml Syringe Luer Lok Tip, Reorder #3039605, BD, Franklin Lakes, NJ 07417. due to Defective Seal: The convenience trays may have open seals, which can adversely impact tray sterility.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Defective Seal: The convenience trays may have open seals, which can adversely impact tray sterility.
Recommended Action
Per FDA guidance
BD notified distributors by an Urgent Product Recall Letter sent via UPS on January 7, 2008. In addition, the firm sent an Urgent Product Recall Letter on January 11, 2008 to customers identified by the distributors. The letter instructed the users to remove the product from its inventory and to return affected products to the firm using an enclosed customer packing list. For additional information, contact 1-888-237-2762.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026