Reported Aug 5, 2020 · Terminated

Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (each) - Product Usage: The laryngoscope is a device…

Teleflex Medical Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: TELEFLEX MEDICAL INC · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437

Is this the product you have?

  • Rusch Greenlite Product Code004551003
  • GTIN14026704663122 (each) -
  • Product UsageThe laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation
Lot codes and dates
  • Lot/Batch Numbers
    • 1812331
    • 1901331
    • 1903331
    • 1905331
    • 1906331
    • 1907331
    • 1908331
    • 1909331
Amount recalled
301085 units

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

Why it was recalled

Breaking at the point of a welded joint

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 31, 2023 · Data as of Sep 19, 4:50 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.