Quidel MicroVue Intact PTH EIA recall
Quidel MicroVue Intact PTH EIA, Model 8044. An enzyme immunoassay for the quantification of Intact Parathyroid Hormone (PTH) in serum.
Why was Quidel MicroVue Intact PTH EIA recalled?
There may be a loss of separation between Calibrators A and B which may impact the assay calibration at the lower end of the assay.
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 068259
- Product
- Quidel MicroVue Intact PTH EIA, Model 8044. An enzyme immunoassay for the quantification of Intact Parathyroid Hormone (PTH) in serum.
- Recalling firm
- Diagnostic Hybrids, Inc.
- Quantity
- 26
- Distribution
- The product was distributed to the following countries: Singapore, Switzerland
- Recall date
- May 2, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)