Program Update Package AutoDELFIA¿ 3.0 recall: Software Issue
Program Update Package AutoDELFIA¿ 3.0, Fluorometer, for clinical use Product Number: 1235-8110 Product Usage: The Wallac 1235 AutoDELFIA automatic…
Why was Program Update Package AutoDELFIA¿ 3.0 recalled?
AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
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?
Batch Code: 649552 OUS: 649552, 649552
- Product
- Program Update Package AutoDELFIA¿ 3.0, Fluorometer, for clinical use Product Number: 1235-8110 Product Usage: The Wallac 1235 AutoDELFIA automatic…
- Recalling firm
- PerkinElmer Health Sciences, Inc.
- Quantity
- 1 unit (US) 2 units (OUS)
- Distribution
- Worldwide Distribution - US Nationwide in the state of MN and countries of China, India, Philippines, France, South Korea, Vietnam, Taiwan, Morocco, Kazachstan, UK, Spain, and Israel,
- Recall date
- February 1, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)