Boston Scientific Corporation: Medical Device Recall in 2024 - (Recall #: Z-3280-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

WALLFLEX ESOPHAGEAL FC 23/28MMX15CM-Wallflex Esophageal Partially Covered and Fully Covered Stent System is Intended for maintaining esophageal luminal patency in esophageal strictures caused by intrinsic and/or extrinsic malignant tumors, and occlusion of concurrent esophageal fistulas Material Number (UPN): M00516750

Product Classification:

Class II

Date Initiated: August 1, 2024

Date Posted: October 2, 2024

Recall Number: Z-3280-2024

Event ID: 95124

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.

Status: Ongoing

Product Quantity: 516 units

Code Information:

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

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of APAC, Canada, EMEA, LATAM.

Voluntary or Mandated:

Voluntary: Firm initiated