Reported Aug 26, 2015 · Terminated

HUDSON RCI, Sheridan Sher-I-BRONCH, Endobronchial Tube (Right sided), Sizes: 28 Fr., 35 Fr., 37 Fr., 39 Fr. and 41 Fr.,…

Teleflex Medical

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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 · 2917 Weck Dr · Research Triangle Park, NC · 27709-0186

Is this the product you have?

  • HUDSON RCI, Sheridan Sher-I-BRONCH, Endobronchial Tube (Right sided)
  • Sizes28 Fr., 35 Fr., 37 Fr., 39 Fr. and 41 Fr., Rx Only, Sterile. Intended for use in thoracic surgery, bronchospirometry, for the administration of bronchial anesthesia and other uses commonly requiring bronchial intubation
Lot codes and dates

5 of 5 products

Products covered by this recall
Model / numberProduct as published
5-16128Lot numbers: 73L1400012, 73K1400582, 73L1400233 and 73A1500039
5-16135Lot numbers: 73B1500259, 73B1500293, 73C1500401, 73C1500426, 01K1300470, 01B1400479, 73D1400498, 73F1400096, 73H1400443, 73J1400117, 73K1400583, 73L1400094, 73A1500205, 73A1500206 and 73B1500258
5-16137Lot numbers: 73B1500354, 73B1500355, 73C1500402 and 73C1500427
5-16139Lot numbers: 73G1400177, 73H1400444, 73L1400095, 73A1500041 and 73A1500203
5-16141Lot numbers: 01L1300156, 01A1400452, 73G1400178, 73G1400510, 73H1400009, 73K1400553 and 73B1500257.
Amount recalled
188,195 total units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

The double swivel connector may crack or separate on the endobronchial tube.

Using this product could cause serious injury, illness or death — stop using it now.

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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 Apr 16, 2018 · Data as of Sep 19, 5:27 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.