Animas Corporation Battery Caps used with insulin pumps and glucose monitoring systems. The pump is used to help maintain blood glucose targets. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Battery Caps used with insulin pumps and glucose monitoring systems. The pump is used to help maintain blood glucose targets.
Brand
Animas Corporation
Lot Codes / Batch Numbers
Part Number: 100-158-01. All units (no serial numbers).
Products Sold
Part Number: 100-158-01. All units (no serial numbers).
Animas Corporation is recalling Battery Caps used with insulin pumps and glucose monitoring systems. The pump is used to help mai due to Unintentional rebooting: Pump products exhibit an intermittent loss of power due intermittent loss of contact between battery cap and battery canister. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Unintentional rebooting: Pump products exhibit an intermittent loss of power due intermittent loss of contact between battery cap and battery canister resulting in the device resetting. The failure of the battery cap may result in failure of the device to administer insulin therapy which may result in hyperglycemia.
Recommended Action
Per FDA guidance
The recalling firm issued a notification letter to the patients with insulin pumps on 8/5/08 to inform them of the problem and that they needed to replace the battery. The recalling firm contacted OneTouch Ping users by telephone on 8/5/08 for this issue and another issue. The recalling firm issued letters to distributors informing them of the problem and notified customers to replace the batteries. In addition, a letter was issued to physicians to alert them of the situation with regard to current patients. Consumers can contact 1-800-423-4087 for additional information or questions.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AR, CA, FL, KY, LA, MA, NE, OH, PA, SC, SD, TN, UT
Page updated: Jan 10, 2026