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Recall Observatory FDA recall evidence

Device product

Ultroid Sterile Disposable Probes sold individually

Z-0785-2017

October 19, 2016

Class II

Product summary

Firm
Ultroid Technologies, Inc.
Event
Event 75055
Status
Terminated
Classification
Class II
Quantity
7,784
Official record key
device-enforcement:Z-0785-2017

Official wording

Reason: Products are not designed, qualified, manufactured, and/or managed under a state of control per internal quality system procedures and external laws, regulations, directives, standards, and/or guidance (such as 21 CFR 820 Quality System Regulation)

Code information: ALL serial numbers and lot numbers sold since January 14, 2003.

Distribution pattern: AL, AR, AZ, CA, CO, CT, DE, FL, GA, ID, IL, KS, LA, MD, ME, MI, MN, NE, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA and Puerto Rico Asturias, Australia, Chile, Greece, Hong Kong, India, Indonesia, Iraq, Japan, Kuwait, Malaysia, Mexico, Nigeria, Qatar, Russia, Slovenia, Spain, Syria, Trinidad, Turkey, UAE, UK, and Vietnam

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Products are not designed, qualified, manufactured, and/or managed under a state of control per internal quality system procedures and external laws, regulations, directives, standards, and/or guidance (such as 21 CFR 820 Quality System Regulation)