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All product recalls associated with Respironics, Inc..
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Medtronic Cardiac Rhythm Disease Management has voluntarily suspended worldwide distribution of the Sprint Fidelis family of defibrillation leads because of the potential for lead fractures. In addition, the company recommends against new implants of the leads (Sprint Fidelis Models: 6930, 6931, 6948, 6949). Medtronic, its Independent Physician Quality Panel, and Bruce Lindsay, M.D., Professor of
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Incorrect micro-organism-- Quality control In-vitro diagnostic test was manufactured with Cryptococcus neoformans (ATCC 76484) instead of Haemophilus parainfluenzae (ATCC 7901).
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Labeling (additional) use instructions: to clarify proper position of cardioPAT device and post-op line to prevent fluid build up from patient's chest
Foreign material: Glass fragments may present in the plastic bag material used to ship components.
Medtronic Cardiac Rhythm Disease Management has voluntarily suspended worldwide distribution of the Sprint Fidelis family of defibrillation leads because of the potential for lead fractures. In addition, the company recommends against new implants of the leads (Sprint Fidelis Models: 6930, 6931, 6948, 6949). Medtronic, its Independent Physician Quality Panel, and Bruce Lindsay, M.D., Professor of
Incorrect micro-organism-- .Quality control In-vitro diagnostic test was manufactured with Cryptococcus neoformans (ATCC 76484) instead of Haemophilus parainfluenzae (ATCC 7901).
Foreign material: Glass fragments may present in the plastic bag material used to ship components.