AB SCIEX API 3200MD" LC/MS/MS System with software recall: Software Issue
AB SCIEX API 3200MD" LC/MS/MS System with software: MultiQuantMD 3.0In vitro diagnostic to identify inorganic or organic compounds (e.g., lead…
Why was AB SCIEX API 3200MD" LC/MS/MS System with software recalled?
Software- AB SCIEX API 3200MD LC/MS/MS SYSTEM with MultiQuantMD 3.0 software may provide incorrect data for patient diagnosis
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?
Serial Numbers: BV20031308, BV20081311, BV20051310, BV20071311, BV20101401, BV20131401
- Product
- AB SCIEX API 3200MD" LC/MS/MS System with software: MultiQuantMD 3.0In vitro diagnostic to identify inorganic or organic compounds (e.g., lead…
- Recalling firm
- Ab Sciex
- Quantity
- 6 units
- Distribution
- FL, NC, OK, PA, TX
- Recall date
- September 17, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)