FDAClass IIIDecember 14, 2016

Barbiturates Intercept Micro-Plate EIA recall

Barbiturates Intercept Micro-Plate EIA (enzyme immunoassay, barbiturate) Product is intended for use by clinical laboratories in the qualitative…

Why was Barbiturates Intercept Micro-Plate EIA recalled?

Shipping error. Cocaine metabolite Microplate distributed instead of Barbiturate Microplate due to incorrect selection of Microplate during manufacturing.

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 # 6654085

Product
Barbiturates Intercept Micro-Plate EIA (enzyme immunoassay, barbiturate) Product is intended for use by clinical laboratories in the qualitative…
Recalling firm
OraSure Technologies, Inc.
Quantity
4 kits
Distribution
Distributed to KS, and VA
Recall date
December 14, 2016
Classification
Class III
Status
Terminated
Agency
FDA (device)
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