Class III — Low Risk

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

Pointe Scientific AutoHDL/LDL Cholesterol Calibrator Recalled by Medtest Holdings, Inc. Due to Vials of the autoHDL/LDL Calibrator were shipped without...

Date: August 10, 2018
Company: Medtest Holdings, 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 Medtest Holdings, Inc. directly.

Affected Products

Pointe Scientific AutoHDL/LDL Cholesterol Calibrator, Catalog Number H7545-CAL - Product Usage: For the calibration of Pointe Scientific s autoHDL and autoLDL Cholesterol Reagent Set in serum or plasma. For in vitro diagnostic use only.

Quantity: 22

Why Was This Recalled?

Vials of the autoHDL/LDL Calibrator were shipped without a vial label.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Medtest Holdings, Inc.

Medtest Holdings, Inc. has 10 total recalls tracked by RecallDetector.

Related Recalls

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