Acceava Mono II Rapid Test Strip recall: Labeling Error
Acceava Mono II Rapid Test Strip (Whole Blood, Serum, Plasma), Catalog No. 92404. Mononucleosis Rapid Test Device a simple test that utilizes an…
Why was Acceava Mono II Rapid Test Strip recalled?
The Positive Control information referencing human plasma as the antibody material described in the product labeling and packaging is incorrect.
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 are affected
- Product
- Acceava Mono II Rapid Test Strip (Whole Blood, Serum, Plasma), Catalog No. 92404. Mononucleosis Rapid Test Device a simple test that utilizes an…
- Recalling firm
- Alere San Diego, Inc.
- Quantity
- N/A
- Distribution
- US
- Recall date
- August 3, 2016
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)