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Terminated

MedMinder Medication Dispenser- Intended to serve as a medication reminder to promote medication adherence with additional feature to communicate with emergency call center.

FDA Recall Z-1254-2022 · Posted None

Recall StatusTerminated
Product CodeILQ
Date Initiated2022-03-28
Date Terminated2024-01-19
Product Quantity2701 units

Reason for Recall

Discontinuation of the Emergency Alert watch or pendant will no longer connect to the emergency alert system for all models. Older Model (legacy) without screen medical alert feature(button) removed

Firm Action

Medminder engaged a third-party vendor to perform the phone calls and notifications. The process was initiated on 03/28/2022. Initial contact via telephone and text message. Formal letter issued first week of April 2022, formal certified letters to all relevant customers notifying them of the removal of the pendant/watch and that it will no longer be supported (will no longer connect to the emergency alert system). . As of this notification, the medical alert pendants and watches will not work when pressed to call for emergency services. Please put in trash. Customers can still use the medical alert feature with the pill dispenser itself or call 911 or any other emergency system available to them. Older models (412 units) without the screen, the medical alert feature using the mechanical button has been removed and should not be relied on and there is no support for the red emergency alert button on your model of the MedMinder pill dispenser, and should not be used to contact emergency services. Please know that you should call 911 in the event of an emergency. If you were scheduled in the past for replacement of the pill dispenser with a newer model, it will be completed as scheduled. Notification letters were issued depending on the model being used by the customers as follows: 1. Letter to newer models regarding the accessory pendant only. 2. Letter to older models regarding the accessory pendant as well as the feature. 3. Introductory letter for subgroup of 29 customer with both older and newer models.

Root Cause

Other

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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