Ultroid Technologies recalls
Ultroid Technologies appears in 4 official U.S. recall notices indexed by RecallRadar, most recently on 2016-12-28.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 4 |
|---|---|
| Published | 2016-12-28 |
| By agency | FDA Device (4) |
| By classification | Class II (4) |
| By status | terminated (4) |
| Distribution named in notices | 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, PR, RI, SC, TN, TX, UT, VA, WA |
Recalls
- Ultroid Mobile Generator/Battery operated unit including the Ultroid Sterile Disposable Probes
FDA Device · Class II · 2016-12-28 · Ultroid Technologies
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 8… - Ultroid Sterile Disposable Probes sold individually
FDA Device · Class II · 2016-12-28 · Ultroid Technologies
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 8… - Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes
FDA Device · Class II · 2016-12-28 · Ultroid Technologies
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 8… - Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes
FDA Device · Class II · 2016-12-28 · Ultroid Technologies
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 8…