BD Vacutainer Multiple Sample and Direct Draw Luer recall
BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes, NJ 07417 USA A sterile non-invasive device used to connect venous access…
Why was BD Vacutainer Multiple Sample and Direct Draw Luer recalled?
BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood leakage and low draw volume.
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?
Marketing Status: Class II, 510K # K991088 Device Listing Number: D030347 Catalog number 367290, 367300 (CE), 368491, and 303380.
- Product
- BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes, NJ 07417 USA A sterile non-invasive device used to connect venous access…
- Recalling firm
- Becton Dickinson & Company
- Quantity
- 37,906,400 units
- Distribution
- Nationwide Distribution
- Recall date
- August 14, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)