Recall · FDA
Becton Dickinson & Company
Becton Dickinson & Company issued a Class II FDA recall (Z-1440-2017) initiated 2016-12-20: Eclipse Hypodermic Needle
| Company | Becton Dickinson & Company |
|---|---|
| Recall number | Z-1440-2017 |
| Classification | Class II |
| Status | Terminated |
| Category | Devices |
| Initiated | 2016-12-20 |
| Product | Eclipse Hypodermic Needle |
| Reason | BD is initiating a Product Advisory for the Eclipse Hypodermic Needle because of safety complaints covering disengagement and needlestick injuries. |
FAQ
What did Becton Dickinson & Company recall?
Eclipse Hypodermic Needle
Why was Becton Dickinson & Company's product recalled?
BD is initiating a Product Advisory for the Eclipse Hypodermic Needle because of safety complaints covering disengagement and needlestick injuries.