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Animas Corporation

Complete recall history across all FDA and CPSC categories — 6 total recalls

Animas Corporation appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (6)

FDA medical device enforcement actions by Animas Corporation

Date Product Reason Class
Jun 10, 2014 Animas Vibe Insulin Infusion Pump. This product is indicated for continuou... Animas determined that the Hebrew language translation in the Vibe Insulin In... Class II
Jan 3, 2013 Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indic... Animas has identified a component issue affecting a small supply of the Anima... Class I
Dec 17, 2012 Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infu... Due to an internal calendar date limit (December 31, 2015) these pumps will c... Class III
Oct 25, 2012 Animas Vibe Insulin Infusion Pump and System. These products are indicated... Animas determined that keypad wear over time was contributing to an increased... Class II
Jul 16, 2012 IR1200, IR1250(IR1200 Plus), 2020 and One Touch(R) Ping(R) Insulin Pump gluco... Wear of the keypad that may lead to damage such as tearing or peeling of the ... Class II
Sep 6, 2011 Animas Vibe Insulin Infusion Pump. This product is indicated for continuou... Calibration factors in the pump overwritten during a programming step. The fo... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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