Atlas FDA

Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and

FDA device recall Z-0955-2020 · posted 2020-02-07 · Open, Classified

Recall details

Recalling firm
Medtronic Inc.
Reason for recall
There have been reported incidents of a loose reservoir that can no longer be locked into the pump. The reservoir can become loose due to a broken or missing retainer ring that prevents a proper lock. If the reservoir is not properly locked into the pump, it could lead to over or under delivery of insulin, which could then result in hypoglycemia or hyperglycemia.
Action taken
On November 21, 2019, Medtronic initiated a recall of MiniMed 600 series insulin pumps with a clear retainer ring design. On October 5, 2021, the firm expanded the recall and issued an "Urgent Field Safety Notification" to all patients and health care providers. The updated notification informs consignees that Medtronic will proactively replace all MiniMed 600 series insulin pumps that have a clear retainer ring design with an equivalent pump that has the updated black retainer ring design. Pumps will be replaced at no charge over the coming months even if the retainer ring is not damaged and regardless of the warranty status of the pump. In addition to providing consignees with this updated recall strategy, the firm asked consignees to take the following actions: ACTIONS REQUIRED BY YOU: 1. Complete and return the attached Confirmation Form to acknowledge that you have reviewed and understood this notification. 2. Medtronic is requesting patients visit [www.medtronicdiabetes.com/PumpRing] and complete the form online, or call us at 1-877-585-0166 to indicate their decision to receive a replacement pump at no charge. Replacement pumps will become available in the coming months and patients will be notified when their pump is ready to ship. Please assist patients in making replacement decision considering the safety risk associated with the retainer ring issue. For additional recall details, please view the following link: https://www.medtronicdiabetes.com/customer-support/product-and-service-updates/notice15-letter
Root cause
Device Design
Status
Open, Classified
Product code
OZO
Distribution
US:AK,AL,AR,AZ,BM,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, VT, WA, WI, WV, WY OUS: France, Germ
Date initiated
2019-11-21
Date posted
2020-02-07
Location
Northridge, CA

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