Reported Feb 25, 2015 · Terminated

R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal…

Teleflex, 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, Inc. · 550 E Swedesford Rd Ste 400 · Wayne, PA · 19087-1601

Is this the product you have?

  • R¿SCH
  • Curved Reinforced Endotracheal TubeRusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated for airway management. The product may be used to reduce the potential for kinking whenever an unusual positioning of the head or neck is required following intubation
Lot codes and dates
  • product codes
    • 103902-000035
    • 103902-000040
    • 103902-000045
    • 103902-000050
    • 103902-000055
    • 103902-000060
    • 103902-000065
    • 103902-000070
    • 103902-000075
  • lot numbers

    263 of 263 codes

    • 13EG10C
    • 13FG15C
    • 13FG34C
    • 13GE30C
    • 13IG03C
    • 13IG31C
    • 13JG22C
    • 13KG11C
    • 13LT18C
    • 14AE04
    • 14AE04C
    • 14CE10
    • 14CE11
    • 14DG05
    • 14FE23C
    • 14HE34
    • 13CG12
    • 13EG11C
    • 13FG03C
    • 13FG32C
    • 13GE29C
    • 13HG16C
    • 13IG15C
    • 13IG31C
    • 13IG32C
    • 13IG34C
    • 13JG14
    • 13JG14C
    • 13KE45
    • 13KG08C
    • 13KG11C
    • 14AE05
    • 14AE05C
    • 14BG15
    • 14BG30
    • 14CE11
    • 14DG05C
    • 14HE34
    • 14IE37C
    • 14IE39
    • 14IE39C
    • 13FG03C
    • 13FG32C
    • 13GE29C
    • 13IG12C
    • 13JG12C
    • 13JG14C
    • 13KG11C
    • 13KG31C
    • 13LG35C
    • 14AG22
    • 14BG09
    • 14CE10C
    • 14CG22
    • 14CG30
    • 14DG07
    • 14DG07C
    • 14EG04
    • 14EG07C
    • 14EG32
Amount recalled
2,292,361

Where it was sold

  • Nationwide

Why it was recalled

Teleflex Medical has issued an advisory notification for the RUSCH Curved Reinforced Endotracheal Tube because of a discrepancy between the labeled cuff diameter and the actual cuff diameter. The actual product cuff diameter meets required specification.

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Jul 30, 2015 · Data as of Sep 19, 4:46 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.