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Recall Observatory FDA recall evidence

Device product

TheraSphere Administration Set, REF OTT-SPE-FP-226 (990226.SPE)

Z-2327-2021

July 23, 2021

Class II

Product summary

Firm
Boston Scientific Corporation
Event
Event 88369
Status
Ongoing
Classification
Class II
Quantity
4980 sets
Official record key
device-enforcement:Z-2327-2021

Official wording

Reason: Potential for leaks and loosening at the patient catheter connection

Code information: GTIN 05060116920253, Lot Numbers: 001E, 002E, 004E, 005E, 006E, 007E, 114E, 690E, 692E

Distribution pattern: Worldwide distribution - US Nationwide and the countries of Belgium, Canada, Germany, Spain, France, United Kingdom/Great Britain, Hong Kong, Ireland, Israel, India, Italy, Netherlands, Poland, Portugal, Saudi Arabia, Singapore, Switzerland, Turkey, and Argentina.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Potential for leaks and loosening at the patient catheter connection