Z-0377-2018 Class II Ongoing
FDA device recall Z-0377-2018 was initiated by Boston Scientific Corporation on Dec 7, 2017 and is designated Class II. Reason for recall: Boston Scientific has received reports of intermittent over-sensing of the Minute Ventilation (MV) sensor signal with certain Boston Scientific pacemaker and cardiac resynchronization therapy… The recall status is ongoing.
Recall Details
- Product Type
- Devices
- Report Date
- Jan 24, 2018
- Initiation Date
- Dec 7, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
Product Description
PROPONENT MRI Pacemaker
Reason for Recall
Boston Scientific has received reports of intermittent over-sensing of the Minute Ventilation (MV) sensor signal with certain Boston Scientific pacemaker and cardiac resynchronization therapy pacemaker systems (pacemakers).
Distribution Pattern
AK, AL, AR, AZ, CA , CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OR, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY, and Puerto Rico Worldwide
Code Information
Model's; L210, L211, and L231 - NOT APPROVED IN US
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0377-2018
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026