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
103902-000035103902-000040103902-000045103902-000050103902-000055103902-000060103902-000065103902-000070103902-000075
- lot numbers
263 of 263 codes
13EG10C13FG15C13FG34C13GE30C13IG03C13IG31C13JG22C13KG11C13LT18C14AE0414AE04C14CE1014CE1114DG0514FE23C14HE3413CG1213EG11C13FG03C13FG32C13GE29C13HG16C13IG15C13IG31C13IG32C13IG34C13JG1413JG14C13KE4513KG08C13KG11C14AE0514AE05C14BG1514BG3014CE1114DG05C14HE3414IE37C14IE3914IE39C13FG03C13FG32C13GE29C13IG12C13JG12C13JG14C13KG11C13KG31C13LG35C14AG2214BG0914CE10C14CG2214CG3014DG0714DG07C14EG0414EG07C14EG32
- product codes
- 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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