Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by Phadia Ab Due to code 7-102 Liquid Sensor Error...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Phadia Ab directly.
Affected Products
Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is fully integrated and automated instrument including software for immunodiagnostic testing. The instrument is designed to handle all steps from sample and reagent handling to processing of results.
Quantity: 387 Instruments
Why Was This Recalled?
code 7-102 Liquid Sensor Error
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Phadia Ab
Phadia Ab has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report