Ad-Tech Medical Instrument Corporation Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Brand
Ad-Tech Medical Instrument Corporation
Lot Codes / Batch Numbers
Item 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
Products Sold
Item 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
Ad-Tech Medical Instrument Corporation is recalling Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these elect due to Incorrect version of labels were used.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect version of labels were used.
Recommended Action
Per FDA guidance
Consignees were sent a "Medical Device Recall" letter dated August 09, 2021. The letter described the problem and the product being recalled. Advised consignees to immediately examine their inventory, quarantine and return the product to AD-Tech. If the product has been further distributed identify customers and notify them of the recall. Requested consignees to complete and return the "Medical Device Recall Return Response" form to their Ad-Tech Clinical Specialist at customersupport@adtechmedical.com; FAX: 262-634-5668 or Telephone 800-776-1555. For questions contact Ad-Tech Clinical Specialist.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026