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Recall Observatory FDA recall evidence

Device product

Alinity s System REF 06P16-01. An automated immunoassay analyzer for In Vitro diagnostic use in blood donor screening, plasma and plasmapheresis screening, and organ donor centers, hospitals, and reference laboratories.

Z-2276-2021

July 12, 2021

Class II

Product summary

Firm
Abbott Laboratories, Inc
Event
Event 88324
Status
Ongoing
Classification
Class II
Quantity
260 systems
Official record key
device-enforcement:Z-2276-2021

Official wording

Reason: A design defect (hardware and software) allows liquid waste pressure to build up and potentially spray users/operators.

Code information: Model Number: LN 06P16-01 Serial numbers AS1001 through AS1330

Distribution pattern: Worldwide distribution. US nationwide, Australia, Bahrain, Belgium, Brazil, China, Colombia, Croatia, Egypt, Germany, Greece, Hong Kong, Hungary, Iran, Ireland, Israel, Italy, Jordan, Kuwait, Mexico, Netherlands, Pakistan, Poland, Portugal, Saudi Arabia, Serbia, Slovenia, South Africa, Spain, Tanzania, United Arab Emirates, United Kingdom, Ukraine and Zimbabwe.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    defect (hardware and software