Reported Oct 8, 2014 · Terminated

Hudson RCI¿ Pediatric Anesthesia Breathing Circuits, Single Patient Use, Rx Only, Product Usage: To administer medical…

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 · 4024 Stirrup Creek Dr · Durham, NC · 27703-9000

Is this the product you have?

  • Hudson RCI¿ Pediatric Anesthesia Breathing Circuits, Single Patient Use, Rx Only
  • Product UsageTo administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Ypiece
Lot codes and dates

12 of 12 products

Products covered by this recall
Model / numberProduct as published
313905Lot #02F1300085
353900Lot #02D1300584
353901Lot #0241300618
353911Lot #02G1300296, 02G1300861, 02F1300729
313901Lot #02G1300088
353811Lot #02E1300090
02E1301383 & 02E1301867
353911Lot #02F1300102 & 02F1300177
353900Lot #02F1302029
353801Lot #02E1300623, 02FF1300098, 02H1300172, 02H1300454, 02H1301128, 02F300180, 02E1301891, 02J1300876, 02H1301838, 02J1302412 & 02B1400324
353901Lot #02E1301378
353901Product Code: 353900, Lot #02E1301892, 02F1300100 and , Lot #02F1302047, 02F1300101 & 2G1300879.
Amount recalled
27,176 units

Where it was sold

Why it was recalled

Stop using this product now

The pediatric breathing circuits can crack prior to and during use.

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

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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 16, 2016 · Data as of Sep 19, 4:49 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.