Aquarius D13S319 Plus Deletion Probe recall
Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb region including most of the…
Why was Aquarius D13S319 Plus Deletion Probe recalled?
There is an error in the chromomap on the package insert.
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 Numbers: 058585, 061111, 061354, 062527
- Product
- Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb region including most of the…
- Recalling firm
- Cytocell Ltd.
- Quantity
- 400
- Distribution
- Worldwide Distribution - US Nationwide AL, CO, FL, HI, IA, IL, IN, KY, MA, MD, MI, MO, MS, NC, NJ, NY, TN, TX, UT, WA, and WI. The products were distributed to the following foreign countries: Canada.
- Recall date
- June 26, 2019
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)