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

Recall Z-0512-2014 — Stryker brand SUPER COMPLIANT 7MM X 15MM, Catalog Number: M003SSC07150; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular Microcatheters are intended to assist

U.S. FDA — Device Enforcement · United States · 2013-11-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0512-2014
Date of alert: 2013-11-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Stryker Neurovascular
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 17010924

Reported risk: Products were shipped labeled with "use by" dates that exceed currently available shelf-life data. All products remain within the earliest expiration date of April 2015.

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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