FDAClass IIIMay 16, 2018

Syva¿ EMIT¿ II Plus 6-Acetylmorphine recall

Syva¿ EMIT¿ II Plus 6-Acetylmorphine Catalog # for 1000 mL: 9R129UL /SMN# 10481483

Why was Syva¿ EMIT¿ II Plus 6-Acetylmorphine recalled?

Incorrect calibrator level listed in qualitative calibration steps

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?

All lots

Product
Syva¿ EMIT¿ II Plus 6-Acetylmorphine Catalog # for 1000 mL: 9R129UL /SMN# 10481483
Recalling firm
Siemens Healthcare Diagnostics, Inc.
Quantity
N/A
Distribution
PA, MA, TX, ME, UT, FL, KS, NH, KY and Foreign
Recall date
May 16, 2018
Classification
Class III
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls