Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ARCHITECT i2000SR System The Abbott ARCHITECT System is intended for Recalled by Abbott Laboratories, Inc Due to Incorrect tubing.
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 Abbott Laboratories, Inc directly.
Affected Products
ARCHITECT i2000SR System The Abbott ARCHITECT System is intended for In Vitro diagnostic use only. The ARCHITECT system is designed to perform automated immunoassay tests, utilizing CMIA (chemiluminescent microparticle assay) detection technology.
Quantity: 65 units
Why Was This Recalled?
Incorrect tubing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Abbott Laboratories, Inc
Abbott Laboratories, Inc has 31 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report