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FDA (Device enforcement)Recalled 2024-08-01class ii

Boston Scientific Corporation: WALLFLEX ESOPHAGEAL FC 23/28MMX15CM-Wallflex Esophageal Partially Covered and Fully Covered Stent System is Intended for maintaining esophageal luminal patency in esopha

Hazard

WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire (OTW) Stent System due to the potential for delivery catheter tip detachment.

Details from the source

Reason for recall: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire (OTW) Stent System due to the potential for delivery catheter tip detachment. Distribution: Worldwide distribution - US Nationwide and the countries of APAC, Canada, EMEA, LATAM. Quantity: 516 units Lot/code info: GTIN: 08714729778080 Lot Numbers: 32809369, 32809370, 32820234 ,32829719, 32837015, 32859849, 32888837, 32888838, 32914768, 32919658, 32919659, 32938991 32956256, 32977683, 32980850, 32986659, 32994875, 32998177, 33014830, 33101458, 33119730, 33176329, 33195046, 33195048 33208043, 33208044, 33218761, 33242625, 33266646, 33266649

UPC codes

08714729778080

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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