| 2026-05-20 | FDA Device | FDA Recall: BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: BARD Dynamic Tip Steerable, Product Number 6DYNTP001; | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: BARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable, Product Number 401905; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable, Product Number 401914; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable, Product Number 401582; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Medtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable, Product Number 401652; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable, Product Number 401923; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: Daig Livewire Steerable, Product Number 401908; REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER | Stryker Sustainability Solutions | Class II | N/A |
| 2026-04-15 | FDA Device | FDA Recall: Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5 | Stryker Sustainability Solutions | Class II | N/A |