Product Safety Recalls

Product Recall Tracker

Ad-Tech Medical Instrument Corporation Recall 88590

Description: Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.

Ad-Tech Medical Instrument Corporation Recall 88590 Information

StatusCompleted
Mandated?Voluntary: Firm initiated
Recall NumberZ-2494-2021
Event ID88590
Event DescriptionAd-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Product TypeDevices
DistributionWorldwide distribution - US Nationwide distribution in the states of DC, FL, MI, NY, PA and TX and the countries of Spain, France, Italy, Greece, Great Britain and Canada.
Quantity69
Recall ReasonIncorrect version of labels were used.
Device Classification20210929
Device Code InfoItem Code & Lot #: L-SRL-10DIN Lot #'s 120340, 122140 and 124140; L-SRL-10DIN-84 Lot #'s 126270 and 127270; L-SRL-12BDIN Lot # 125250; L-SRL-16BDINLot #124150; L-SRL-20DINLot # 127060; L-SRL-32BDIN Lot # 126070 L-SRL-4DIN Lot #'s 123050, 129150 and 120250; L-SRL-64BDIN Lot #127270; L-SRL-6DINLot #'s 128060 and 120160; L-SRL-8DIN Lot #'s 128150 and 124050; L-SRL-8DIN-11 Lot # 125170
Center Classification Date20210920
Recall Initiation Date20210809
Recalling FirmAd-Tech Medical Instrument Corporation
Initial Notification E-Mail
Similar To

© 2021 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.