Class III — Low Risk

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

Animas(R) 2020 Recalled by Animas Corporation Due to Due to an internal calendar date limit (December...

Date: December 17, 2012
Company: Animas Corporation
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 Animas Corporation directly.

Affected Products

Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous subcutaneous infusion of insulin.

Quantity: 37,998

Why Was This Recalled?

Due to an internal calendar date limit (December 31, 2015) these pumps will cease to operate on January 1, 2016, and will result in a call service alarm that is displayed on the pump display.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Animas Corporation

Animas Corporation has 6 total recalls tracked by RecallDetector.

Related Recalls

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