Dimension Vista LOCI Progesterone recall
Dimension Vista LOCI Progesterone; Catalog Number: K6464; Siemens Material Number: 10461743 Product Usage: For in vitro diagnostic use in the…
Why was Dimension Vista LOCI Progesterone recalled?
DHEA-S causes falsely elevated progesterone 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?
16193BB 16200BA 16214BA 16235BB 16250BA 16270BA 16291BA 16319AA
- Product
- Dimension Vista LOCI Progesterone; Catalog Number: K6464; Siemens Material Number: 10461743 Product Usage: For in vitro diagnostic use in the…
- Recalling firm
- Siemens Healthcare Diagnostics, Inc
- Quantity
- 1148
- Distribution
- US Nationwide distribution including Puerto Rico
- Recall date
- March 15, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)