Ad-Tech TECH ATTACH Cable Recalled Due to Incorrect Labeling
Ad-Tech Medical Instrument Corporation is recalling TECH ATTACH Cables due to incorrect labeling. The cables connect electrodes to third-party monitors and stimulators.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class II medical device labeling error with no reported illnesses or injuries. Per severity rubric, minor labeling errors are classified as Moderate (Score 2).
Plain-English summary
Ad-Tech Medical Instrument Corporation is recalling Ad-Tech TECH ATTACH Cables (Item Code L-DC-10DIN, Lot Numbers 121240 and 126270). These cables are designed to connect electrodes to third-party monitors and stimulators.
The recalled cables were produced with incorrect versions of the product labels.
The affected cables have been distributed worldwide, including in the United States (Washington DC, Florida, Michigan, New York, Pennsylvania, and Texas) and internationally (Spain, France, Italy, Greece, Great Britain, and Canada).
Users of the affected cables should discontinue use and contact Ad-Tech Medical Instrument Corporation for replacement or further guidance.
The recalled product
- Product
- Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
- Manufacturer
- Ad-Tech Medical Instrument Corporation
- Category
- Medical Device — Electrode Cable
- Hazard
- Affected units
- 8
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Item Code & Lot #: L-DC-10DIN Lot #'s 121240 and 126270.
Distribution
Part of a larger recall action
This product is one of 3 recalled by Ad-Tech Medical Instrument Corporation under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 3 products in this recall →Related recalls
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