Eclipse Hypodermic Needle recall
Eclipse Hypodermic Needle
Why was Eclipse Hypodermic Needle recalled?
BD is initiating a Product Advisory for the Eclipse Hypodermic Needle because of safety complaints covering disengagement and needlestick injuries.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
N/A
- Product
- Eclipse Hypodermic Needle
- Recalling firm
- Becton Dickinson & Company
- Quantity
- 263 mm units
- Distribution
- US Nationwide
- Recall date
- March 22, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)