FAS-LOC 6 Foot Disposable Extension Cable with Safe Connect/Screw Down — Class II medical device recall Z-1441-2014
Terminated recall by Remington Medical Inc., reported 2014-04-16, distributed nationwide. Remington Medical discovered an error on the FL-601-97 IFU; part number IFU-RM-0154. Specifically, the polarit
| Recall number | Z-1441-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Remington Medical Inc., Alpharetta, GA, United States |
| Recall initiated | 2014-03-05 |
| Classified | 2014-04-09 |
| Reported by FDA | 2014-04-16 |
| Terminated | 2018-04-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 41,499 cables |
| Lot numbers | 131901, 132262, 132263, 132533, 132693, 132694, 132833, 132835, 132986, 133171 |
Product
FAS-LOC 6 Foot Disposable Extension Cable with Safe Connect/Screw Down. Electrical extension cable intended to transmit signal from, or power or excitation signal to patient connected electrodes. The cable is a sterile, disposable device.
Reason for recall
Remington Medical discovered an error on the FL-601-97 IFU; part number IFU-RM-0154. Specifically, the polarity for the black chuck in the picture is wrong. It shows (+), but should show (-).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1441-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.