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Recall Observatory FDA recall evidence

Device product

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

Z-3281-2024

August 01, 2024

Class II

Product summary

Firm
Boston Scientific Corporation
Event
Event 95124
Status
Ongoing
Classification
Class II
Quantity
297 units
Official record key
device-enforcement:Z-3281-2024

Official wording

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

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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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