Alere Cholestech LDX Calibration Verification recall
Alere Cholestech LDX Calibration Verification, 4 vial set, Catalog Number: 88770 Alere Cholestech LDX Calibration Verification (hereafter referred to…
Why was Alere Cholestech LDX Calibration Verification recalled?
Out of range (increased) HDL Cholesterol results.
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#271097, 298148, and 301886
- Product
- Alere Cholestech LDX Calibration Verification, 4 vial set, Catalog Number: 88770 Alere Cholestech LDX Calibration Verification (hereafter referred to…
- Recalling firm
- Alere San Diego, Inc.
- Quantity
- 614 kits
- Distribution
- Worldwide Distribution - USA (nationwide) Puerto Rico and South Korea.
- Recall date
- February 6, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)