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Orantech

Orantech Inc. · Model TA-MQ700-2AD03 · UDI-DI 06970706367278

IKD
6
510(k) clearances
459
Adverse events (6 deaths)
11
Recalls
218
Facilities

Description

GE Marquette Compatible,Use with YSI700 reusable probe, 0.3M

Recalls

DateFirmReason
2024-07-02Stryker Sustainability SolutionsDisposable 5 lead cable and lead wire system package that should contain lead systems, lead telemetry systems and a dual connect cable, may in fact contain, different ECG Leads, wh
2021-08-09Ad-Tech Medical Instrument CorporationIncorrect version of labels were used.
2021-08-09Ad-Tech Medical Instrument CorporationIncorrect version of labels were used.
2021-08-09Ad-Tech Medical Instrument CorporationIncorrect version of labels were used.
2019-02-22GE Healthcare, LLCThe Integrated ECG cable with 3-lead leadwires can short circuit during defibrillation and conduct 25% of the defibrillation energy away from the patient.
2017-03-31Oscor, Inc.The Reusable Oscor ATAR extension cables could separate from the connector during use.
2017-03-31Oscor, Inc.The Reusable Oscor ATAR extension cables could separate from the connector during use.
2016-03-29Ad-Tech Medical Instrument CorporationAd-Tech is recalling unopened/unused sterile cables intended to be used only with all compatible Ad-Tech electrodes for the purpose of connecting these electrodes to third party mo
2011-06-01St. Jude MedicalSt. Jude Medical is recalling a single lot (3334664) of Supreme Electrophysiology Extension Cable which were packaged with a Quadripolar cable instead of a hexapolar Cable. St. J
2011-02-08Vermed, Inc.Vermed kits contain a product component (Triad Alcohol Prep Pads) recalled due to potential Bacillus cereus contamination.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.