Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0402-2013 — Freedom Cordless LED Light System. Freedom System, Standard Length, Part Number 910863-1, Serial Numbers 77001000-77003470 and Freedom System, Long Length, Part Number 910863-2, Serial Numbers 77001000-77003470. Freedom Cordless LED Light System is a Class I Medical Device. The device listing nu

U.S. FDA — Device Enforcement · United States · 2011-11-17 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0402-2013
Date of alert: 2011-11-17
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Kerr Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 77001000

Reported risk: The firm recalled the Freedom Cordless LED Headlight because some units were assembled with an incorrect component in the control board electronics that may cause some Freedom Cordless LED Headlight units to become warm to the touch; however, no skin damage will occur.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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