Ultroid Technologies, Inc. Recall: Ultroid Hemorrhoid Management Systems 110/220 VAC and p
Ultroid Technologies, Inc. Recall: Ultroid Hemorrhoid Management Systems 110/220 VAC and p is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Ultroid Technologies, Inc.; Product: Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile
| Recalling firm | Ultroid Technologies, Inc. |
|---|---|
| Product | Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes |
| Reason for recall | 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) |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | 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, T |
| Recall initiated | 20161019 |
| Recall number | Z-0782-2017 |
| Category | device |
| State | FL |
| Country | United States |
$29/mo
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