Boston Scientific Corporation: Medical Device Recall in 2024 - (Recall #: Z-3281-2024)

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 PC ESOPH STENT 18/23MM X 103MM- 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): M00516900

Product Classification:

Class II

Date Initiated: August 1, 2024

Date Posted: October 2, 2024

Recall Number: Z-3281-2024

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: 297 units

Code Information:

GTIN: 08714729765240 Lot Numbers: 32759902, 32780160, 32830094, 32865976, 32868557, 32875121, 32891029, 32898065, 32898066, 32906414, 32915745, 32938540 32966004, 32977682, 32985473, 33026702, 33026704, 33036452, 33036453, 33045964, 33056440, 33119731, 33120913, 33167136 33169265, 33169266, 33169267

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated