Class III — Low Risk

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

ADVIA Centaur Intact PTH Calibrator (6 pack) Recalled by Siemens Healthcare Diagnostics, Inc Due to PTH Calibrator packaged with only high calibrator.

Date: August 16, 2013
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

ADVIA Centaur Intact PTH Calibrator (6 pack); Catalog Number: SMN 10492387 For in vitro diagnostic use in calibrating Intact PTH assays on the ADVIA Centaur Systems.

Quantity: 595 kits total (5 kits with packaging error)

Why Was This Recalled?

PTH Calibrator packaged with only high calibrator.

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 118 total recalls tracked by RecallDetector.

Related Recalls

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