MiniMed 740G Insulin Pump (O.U.S. Version)
Reported: July 20, 2022 Initiated: May 23, 2022 #Z-1357-2022
Product Description
MiniMed 740G Insulin Pump (O.U.S. Version)
Reason for Recall
Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of the insulin infusion pumps.
Details
- Recalling Firm
- Medtronic MiniMed
- Units Affected
- 40 pumps
- Distribution
- U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VI, VT, WA, WI, WV, and WY O.U.S.: Not provided
- Location
- Northridge, CA
Frequently Asked Questions
What product was recalled? ▼
MiniMed 740G Insulin Pump (O.U.S. Version). Recalled by Medtronic MiniMed. Units affected: 40 pumps.
Why was this product recalled? ▼
Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of the insulin infusion pumps.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 20, 2022. Severity: Moderate. Recall number: Z-1357-2022.
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