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

Recall Z-2587-2017 — Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel and aluminum rods that are coated with a blue PVC or polypropylene outer covering and are designed to be placed inside an endotracheal tube to obtain a desired shape during intubatio

U.S. FDA — Device Enforcement · United States · 2017-05-11 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2587-2017
Date of alert: 2017-05-11
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Teleflex Medical
Product category: device
Product type: Devices

Reported risk: Product size listed on the labeling is incorrect.

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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