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Becton Dickinson & Co. recalls BBL Port A Cul tubes with Swabs Sterile Pack, catalog number 221607. For patient sample collection.
Recalled June 17, 2015 · FDA recall Z-1747-2015 · Becton Dickinson &
Hazard
The products may exhibit indications of excessive oxidation. Excessive oxidation may affect the viability of anaerobic microorganisms. · FDA Class II
Units
92,710 units
Sold at
US Nationwide distribution in AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NV, NY, OH, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY.
Description
The products may exhibit indications of excessive oxidation. Excessive oxidation may affect the viability of anaerobic microorganisms.
Product
BBL Port A Cul tubes with Swabs Sterile Pack, catalog number 221607. For patient sample collection.
Manufacturer(s)
Becton Dickinson & Co.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →