Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Siemens Dimension Vista(R) Alkaline Phosphatase (ALP) Calibrator The ALP CAL Recalled by Siemens Healthcare Diagnostics, Inc. Due to Correlation slope bias and accuracy shift

Date: October 10, 2012
Company: Siemens Healthcare Diagnostics, Inc.
Status: Terminated
Source: FDA (Device)

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 Siemens Healthcare Diagnostics, Inc. directly.

Affected Products

Siemens Dimension Vista(R) Alkaline Phosphatase (ALP) Calibrator The ALP CAL is an in vitro diagnostic product for the calibration of the Alkaline Phosphatase method on the Dimension Vista" System.

Quantity: 1985 cartons

Why Was This Recalled?

Correlation slope bias and accuracy shift

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc. has 452 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report