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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 26 Results
510(K) Number: K030187
 
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Medtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
Daig Livewire Steerable, Product Number 401923; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
Daig Livewire Steerable, Product Number 401914; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
Daig Livewire Steerable, Product Number 401908; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
Daig Livewire Steerable, Product Number 401905; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
Daig Livewire Steerable, Product Number 401652; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
Daig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
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