FDA recall record

Advanced Sterilization Products STERITITE Containers: STERITITE Container Kit, 1/4 size, 3" recall — FDA Z-0434-2014

Advanced Sterilization Products (ASP) is recalling the SteriTite containers because they do not have consistent data to show that sterility assurance…

Class IIIclassification
Z-0434-2014official record ID
Dec 11, 2013report date

Recall record at a glance

Official recordZ-0434-2014
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAdvanced Sterilization Products
Report dateDec 11, 2013
Recall initiation dateOct 3, 2013
Quantity267 units total (252 units in US)
LocationIrvine, CA, United States

Official product description

STERITITE Containers: STERITITE Container Kit, 1/4 size, 3" high, product code: 13902; STERITITE Mini Mid Size, 3" high, product code: 13903; STERITITE Container Kit, 1/2 size, 4" high, product code: 13904; STERITITE Container Kit, 3/4 size, 4" high, product code: 13905; STERITITE Container Kit, Full size, 4" high, product code: 13906. The ASP STERITITE sealed container system provides an efficient and cost-effective way to package and protect surgical instruments for sterilization, transportation, storage, and aseptic presentation of contents.

Why the product was recalled

Advanced Sterilization Products (ASP) is recalling the SteriTite containers because they do not have consistent data to show that sterility assurance level of 10(-6) is achieved during the half-cycle test runs on new, unprocessed containers.

Distribution information

Worldwide Distribution - USA (nationwide) and the countries of Australia, Vietnam, Thailand, Malaysia, China, Korea (South), Mexico, Spain, Singapore, Hong Kong and Portugal.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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