FDAClass IIJune 15, 2016

Oxoid Nitrocefin recall

Oxoid Nitrocefin (+ Reconstitution Fluid Batch) REF: SR0112C, Oxoid Ltd. For the rapid chromogenic detection of beta-lactamase activity in bacterial…

Why was Oxoid Nitrocefin recalled?

Individual bottles of product may produce weak beta-lactamase reactions. Use may result in delayed or false negative reporting.

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 1717357 Exp: 31Aug2017

Product
Oxoid Nitrocefin (+ Reconstitution Fluid Batch) REF: SR0112C, Oxoid Ltd. For the rapid chromogenic detection of beta-lactamase activity in bacterial…
Recalling firm
Remel Inc
Quantity
2 units were imported and distributed domestically
Distribution
US distribution in MO.
Recall date
June 15, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
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