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

Recall Z-1287-2016 — NecLoc Extrication Collar Product Usage: Necloc collars are applied to patients afflicted with cervical injuries to ensure immobilization.

U.S. FDA — Device Enforcement · Iceland · 2016-02-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1287-2016
Date of alert
2016-02-24
Country / jurisdiction
Iceland
Risk level
Class II
Risk type
recall
Brand
Ossur H / F
Product category
device
Product type
Devices
Reported risk: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve Gray, NecLoc Extrication Collar, Rebound Cartilage, Rebound Cartilage Custom, Rebound Air Walker, Rebound Diabetic Walker, Back Support Suspenders Clip on Black, Back Support Suspenders Sew On Black, Extreme Custom, Unloader Custom XT, Unloader Custom Lite, Unloader Custom, and Papoose Infant Spine Immobilizers because the p
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.

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