Boston Scientific Corporation: Medical Device Recall in 2024 - (Recall #: Z-3275-2024)

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 18/23-25MMX10CM- Wallflex Esophageal Partially Covered (PC) and Fully Covered (FC) Stent System 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): M00516700

Product Classification:

Class II

Date Initiated: August 1, 2024

Date Posted: October 2, 2024

Recall Number: Z-3275-2024

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: 231 units

Code Information:

GTIN: 08714729778035 Lot Numbers: 32779260, 32790021, 32817917, 32860922, 32906415, 32966005, 32967262, 33026701, 33026703, 33077154, 33077157, 33085584 33147800, 33156072, 33218764, 33256093

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated