FDAClass IIIDecember 13, 2017

BD PhoenixTM AP recall

BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standardize ID…

Why was BD PhoenixTM AP recalled?

Potential unexpected movement of robot arm

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?

Serial Numbers: AP0447, AP0448, AP0449, AP0450, AP0451, AP0458 & AP0463.

Product
BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standardize ID…
Recalling firm
Becton Dickinson & Co.
Quantity
7 units
Distribution
Worldwide Distribution - US including CA, NC & TN Internationally: Canada
Recall date
December 13, 2017
Classification
Class III
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls