ClearanceBrief
Recall Z-0542-2024 ยท BZD Ventilator, Non-Continuous (Respirator)

ResMed Ltd.

AirFit F30i Full Face Mask and User Guide

DateDec 21, 2023 (initiated Nov 20, 2023)
StatusOpen, Classified
ReasonMasks non-invasive interface for channeling airflow to patients have magnets that have potential magnetic interference with active medical implants that interact with magnets, and metallic implants/objects containing ferromagnetic material so contraindications and warnings about safe distance to medical devices/implants are being updated for patients using masks or anyone in close physical contact
Root causeDevice Design
ActionOn 11/20/23, "Urgent Field Safety Notices" and FAQs were placed on the firms website at www.resmed.com/magnetupdate, and these notices were emailed to healthcare providers, and distributors who were asked to do the following: 1) Provide a copy of this notice and the physician letter to prescribing physicians, and/or any other relevant healthcare professionals, notifying them of the updated labeling (contraindications and warning). 2) Provide a copy of the patient letter to all patients currently using an affected mask with magnets, notifying them of the updated labeling (contraindications and
Quantity2,037,323
DistributionUS nationwide distribution including Puerto Rico, Guam, and Virgin Islands. OUS (foreign) countries of: AE, AR, AT, AU, BB, BD, BE, BG, BH, BM, BR, CA, CH, CL, CN, CO, CW, CY, CZ, DE, DK, DO, DZ, EC, EE, EG, ES, FI, FO, FR, GB, GF, GG, GL, GP, GR, GT, GY, HK, HN, HR, HU, ID, IE, IL, IM, IN, IR, IS,
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K183512Moore Park Mask
Resmed, Ltd., May 7, 2019