FDAClass IIAugust 31, 2022

a. MMS - IMMUNOSTICS INC McKesson Rapid Test Kit recall

a. MMS - IMMUNOSTICS INC McKesson Rapid Test Kit Consult Colorectal Cancer Screening Fecal Occult Blood Test (iFOB or FIT) Stool Sample 25 Tests…

Why was a. MMS - IMMUNOSTICS INC McKesson Rapid Test Kit recalled?

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA 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?

GTIN: a. 10612479219417; 20612479198368. b. 10612479226132; 20612479225569. c. 10612479226125; 20612479225552

Product
a. MMS - IMMUNOSTICS INC McKesson Rapid Test Kit Consult Colorectal Cancer Screening Fecal Occult Blood Test (iFOB or FIT) Stool Sample 25 Tests…
Recalling firm
Mckesson Medical-Surgical Inc. Corporate Office
Quantity
boxes: a. 20 b. 21 c. 4
Distribution
US Nationwide
Recall date
August 31, 2022
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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