FDAClass IINovember 27, 2019

BD Posiflush Pre-Filled Normal Saline Syringes recall

BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547

Why was BD Posiflush Pre-Filled Normal Saline Syringes recalled?

Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.

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?

Lot Number: 9142881 UDI: 50382903065474

Product
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
Recalling firm
Becton Dickinson & Company
Quantity
1,632,000
Distribution
Distribution US Nationwide and Canada
Recall date
November 27, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
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