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Churchill Medical Systems, Inc. recalls 4" Microbore Double Lumen Set with Bionector, Product Code: BN-208 Accessory device used to administer medical fluids
Recalled April 29, 2015 · FDA recall Z-1469-2015 · Churchill Medical Systems
Hazard
Potential for leaking caused by insufficient bond between needleless device and female luer. · FDA Class II
Units
2350
Sold at
Nationwide Distribution including TX, OH, NY, CA, UT, PA, MA, NY, VA, and IL.
Description
Potential for leaking caused by insufficient bond between needleless device and female luer.
Product
4" Microbore Double Lumen Set with Bionector, Product Code: BN-208 Accessory device used to administer medical fluids
Manufacturer(s)
Churchill Medical Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →