Advance Dx 100 Blood Collection Card Quantity 25 recall
Advance Dx 100 Blood Collection Card Quantity 25 REF CMT01 Advance Dx 100 Blood Collection Card and Foil Bags Quantity 500 Cards and Foil Bags REF…
Why was Advance Dx 100 Blood Collection Card Quantity 25 recalled?
Due to high glucose test results when using the blood collection cards.
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?
Product Catalog Number: CMT01 GTIN: 1061C010890976 Lot Number: PPD02102 V6
- Product
- Advance Dx 100 Blood Collection Card Quantity 25 REF CMT01 Advance Dx 100 Blood Collection Card and Foil Bags Quantity 500 Cards and Foil Bags REF…
- Recalling firm
- Advance Dx, Inc.
- Quantity
- 179,750 cards
- Distribution
- U.S. Nationwide distribution in the states of MD and NC.
- Recall date
- August 18, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)