[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 34.204.191.0. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Limit 200 characters
Limit 25 characters
Conflicts of Interest Disclosure

Identify all potential conflicts of interest that might be relevant to your comment.

Conflicts of interest comprise financial interests, activities, and relationships within the past 3 years including but not limited to employment, affiliation, grants or funding, consultancies, honoraria or payment, speaker's bureaus, stock ownership or options, expert testimony, royalties, donation of medical equipment, or patents planned, pending, or issued.

Err on the side of full disclosure.

If you have no conflicts of interest, check "No potential conflicts of interest" in the box below. The information will be posted with your response.

Not all submitted comments are published. Please see our commenting policy for details.

Limit 140 characters
Limit 3600 characters or approximately 600 words
    Views 3,539
    Citations 0
    Original Investigation
    December 20, 2019

    Outcomes Before and After the Recall of a Heart Failure Pacemaker

    Author Affiliations
    • 1Minneapolis Heart Institute Foundation, Minneapolis, Minnesota
    • 2Minneapolis Heart Institute, Abbott Northwestern Hospital, Minneapolis, Minnesota
    JAMA Intern Med. 2020;180(2):198-205. doi:10.1001/jamainternmed.2019.5171
    Key Points

    Question  Do the medical device industry and the US Food and Drug Administration (FDA) provide timely information about product defects so that patients and their physicians can make fully informed decisions regarding management?

    Findings  In this case series, the outcomes of 90 patients before and after the recall of a cardiac resynchronization therapy pacemaker in November 2015 were examined along with review of the FDA Manufacturer and User Facility Device Experience database and showed that the manufacturer and the FDA were aware of battery and wire connection defects for more than 1 year before patients began to develop serious adverse clinical events because of abrupt loss of pacing. The information included in the recall notification was incomplete, and the FDA underestimated the criticality of the pacemaker’s defects.

    Meaning  The medical device industry and the FDA should focus on early recognition of device defects and fully and promptly disclose vital information to patients and their caregivers.

    Abstract

    Importance  Timely and complete disclosure of medical device defects is necessary to manage patient care safely and effectively.

    Objectives  To determine if the manufacturer’s recommendations following the recall of a medical device were timely and complete, the follow-up information and data provided to patients and physicians were adequate for managing patient care, and the actions taken by the US Food and Drug Administration (FDA) regarding the recall were appropriate.

    Design, Setting, and Participants  This single-center retrospective case series included 90 of 448 patients who were implanted with a cardiac resynchronization therapy pacemaker at the Minneapolis Heart Institute from May 2003 through January 2011; this pacemaker was recalled in November 2015. In addition, returned product reports submitted by the manufacturer to the FDA via the Manufacturer and User Facility Device Experience (MAUDE) database from January 2008 through December 2018 were analyzed.

    Main Outcomes and Measures  Clinical outcomes were serious adverse clinical events that occurred before and after the November 2015 recall notifying physicians and patients that the device’s battery could fail unexpectedly because of high internal impedance. Technical outcomes were signs and causes of failure.

    Results  Five of 90 patients observed during 2015 experienced syncope when their pacemakers stopped pacing owing to battery or wire connection defects prior to the recall. Of the 90 patients, 37 (41%) were men, and the median (interquartile range) age at implantation was 71.3 (66.1-78.2) years. Analysis of the MAUDE data revealed that battery failures prior to the recall were associated with serious adverse events that included 1 death, 1 cardiac arrest, 5 syncopal attacks, and 6 heart failure exacerbations; 3 additional prerecall syncopal events were caused by wire connection defects. The manufacturer and the FDA were aware of the battery and wire connection defects for 19 months before issuing the recall, yet the wire connection problem was not included in the advisory and physicians were not informed that interrogating the pacemaker could result in loss of pacing. The FDA classified the recall as class II rather than the more critical class I.

    Conclusions and Relevance  This case series study of patients implanted with a defective pacemaker found that the pacemaker recall was delayed and that subsequent communications did not include all critical information needed for safe and effective patient care. These findings should prompt reforms in how the medical device industry and the FDA manage future medical device recalls.

    ×