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Teleflex Medical recalls Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,
Recalled June 14, 2017 · FDA recall Z-2251-2017 · Teleflex Medical
Hazard
Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device. · FDA Class II
Units
1150 units
Sold at
CA, CT, FL, IL, IN, MD, MI, MN, MO, MS, NC, NJ, NY, NV, OH, PA, TX, VA, WI and WV.
Description
Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device.
Product
Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →