Skip to content
Recall Observatory FDA recall evidence

Device product

Vysis CLL FISH Probe Kit with the following components: Vysis LSI p53 SpectrumOrange/ATM, SpectrumGreen and LSI D13S319, SpectrumOrange/ 13q34, SpectrumAqua/CEP 12 SpectrumGreen Probes

Z-2576-2021

August 04, 2021

Class II

Product summary

Firm
Abbott Molecular, Inc.
Event
Event 88565
Status
Terminated
Classification
Class II
Quantity
186 units
Official record key
device-enforcement:Z-2576-2021

Official wording

Reason: Potential for Vysis CLL FISH Probe Kits not detecting 13q deletions in known positive patient samples.

Code information: UDI: (01)00884999042780(10)XXXXX(17)211015(240)04N02-021; US Distribution: Part Number 04N02-021, Lot Numbers 517086, 518656; International Distribution: List/Part Numbers (Lot Number): 04N02-021 (517086, 518656), 04N02-022 (517516, 519303), 05J83-001/Part 32-191025 (517068).

Distribution pattern: Worldwide distribution - US Nationwide distribution in the states of AZ, CA, FL, GA, IL, IN, KY, MI, MN, MA, NC, NJ, NM, NY, OH, PA, TN, TX, UT, VA, VT, WA, WI and the countries of Australia, Belgium, Brazil, Canada, China, Costa Rica, Czech Republic, Estonia, Germany, Hong Kong, Israel, Italy, Kazakhstan, Netherlands, Philippines, Poland, Saudi Arabia, Slovenia, South Africa, South Korea, Spain, United Kingdom, Uruguay.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Potential for Vysis CLL FISH Probe Kits not detecting 13q deletions in known positive patient samples.