Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Johnson & JohnsonLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record. See the Johnson & Johnson group view.
As of Nov 13, 2026, FDA's public records list Animas Corporation with 10 510(k) clearances and 6 device recalls. The most recent is a device recall dated Jun 10, 2014: Animas Vibe Insulin Infusion Pump. This product is indicated for continuous subcutane….
| Date | Record | Source |
|---|---|---|
| Jun 10, 2014 | Animas Vibe Insulin Infusion Pump. This product is indicated for continuous subcutaneous infusion of insulin for the treatment of diabeteClass II · Animas determined that the Hebrew language translation in the Vibe Insulin Infusion Pump was incorrect and could lead to | Device recalls |
| Jan 3, 2013 | Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated for continuous subcutaneous infusion of insulin for the trClass I · Animas has identified a component issue affecting a small supply of the Animas(R) 2020 insulin pumps. The component iss | Device recalls |
| Dec 17, 2012 | Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous subcutaneous infusion of iClass III · Due to an internal calendar date limit (December 31, 2015) these pumps will cease to operate on January 1, 2016, and wil | Device recalls |
| Oct 25, 2012 | Animas Vibe Insulin Infusion Pump and System. These products are indicated for continuous subcutaneous infusion of insulin for the treatmClass II · Animas determined that keypad wear over time was contributing to an increased complaint rate associated with damaged key | Device recalls |
| Jul 16, 2012 | IR1200, IR1250(IR1200 Plus), 2020 and One Touch(R) Ping(R) Insulin Pump glucose management system. The device is intended to deliver insuClass II · Wear of the keypad that may lead to damage such as tearing or peeling of the edge of the keypad from the pump. | Device recalls |
| Sep 6, 2011 | Animas Vibe Insulin Infusion Pump. This product is indicated for continuous subcutaneous infusion of insulin for the treatment of diabeteClass II · Calibration factors in the pump overwritten during a programming step. The force sensor could send a lower signal value | Device recalls |
| Jun 24, 2008 | SYMPHONY GLUCOSE MANAGEMENT SYSTEMK080639 · LZG | 510(k) clearances |
| May 15, 2008 | EZ MANAGER MAX DIABETES MANAGEMENT SOFTWAREK080587 · MRZ | 510(k) clearances |
| Mar 30, 2007 | EZMANAGER MAX DIABETES MANAGEMENT SOFTWAREK063674 · LZG | 510(k) clearances |
| Dec 10, 2004 | ANIMAS MODEL IR1250 INSULIN INFUSION PUMPK042873 · LZG | 510(k) clearances |
| Oct 16, 2003 | MODEL IR 1200 INSULIN PUMPK032257 · LZG | 510(k) clearances |
| Jun 5, 2003 | EZMANAGER PLUSK022394 · LZG | 510(k) clearances |
| Jun 4, 2002 | ANIMUS EZSERTER INFUSION SET INSERTERK021700 · KZH | 510(k) clearances |
| May 29, 2002 | MODEL R1000 IR INSULIN PUMP, EZLINK SOFTWARE, SERMON SOFTWARE, R1000 IR DOWNLOAD CRADLE, AND SERIAL INTERFACE ADAPTOR DOK021439 · LZG | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
