Becton Dickinson & Company BD Hypodermic Syringe 10 ml, eccentric tip. Catalog (Ref No.) 305482 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BD Hypodermic Syringe 10 ml, eccentric tip. Catalog (Ref No.) 305482
Brand
Becton Dickinson & Company
Lot Codes / Batch Numbers
Catalog (Ref No.) 305482 100/package UDI 00382903054824 Lot # 8142303 exp date 31-May-2023
Products Sold
Catalog (Ref No.) 305482 100/package UDI 00382903054824 Lot # 8142303 exp date 31-May-2023
Becton Dickinson & Company is recalling BD Hypodermic Syringe 10 ml, eccentric tip. Catalog (Ref No.) 305482 due to The product packaging for the 10 ml eccentric tip syringe may exhibit open seals. An open seal impacts package integrity and potentially compromises . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The product packaging for the 10 ml eccentric tip syringe may exhibit open seals. An open seal impacts package integrity and potentially compromises sterility of the syringe.
Recommended Action
Per FDA guidance
On 01/13/2020 BD issued an Urgent Medical Device Recall notices to distributors via letters and via e-mail. Distributors are requested to identify their customers and provide BD a customer list so that BD can undertake further communication to the users. BD will distribute the recall communication to the distributors customers via FedEx upon receiving the customer information from the distributors. A copy of the BD product recall customer letter will be provided to distributors, in the case they opt to contact their customers directly.
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