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Teleflex Medical recalls HUDSON RCI, Sheridan, SHER-I-SWIV and SHER-I-SWIV/FO Double Swivel, Rx Only, Sterile. Used temporarily to make rigid
Recalled August 26, 2015 · FDA recall Z-2370-2015 · Teleflex Medical
Hazard
The double swivel connector may crack or separate on the endobronchial tube. · FDA Class I
Units
188,195 total units
Sold at
Worldwide Distribution - US (nationwide) and the countries of: The Bahamas, Belgium, Argentina, Canada, China, India, Japan, South Korea, Mexico, New Zealand and Vietnam.
Description
The double swivel connector may crack or separate on the endobronchial tube.
Product
HUDSON RCI, Sheridan, SHER-I-SWIV and SHER-I-SWIV/FO Double Swivel, Rx Only, Sterile. Used temporarily to make rigid a flexible tracheal tube to aid its insertion into a patient.
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →