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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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BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
BARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
BARD Dynamic Tip Steerable, Product Number 6DYNTP001; 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER 2 05/13/2026 FEI # 3009350690
Stryker Sustainability Solutions
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