Z-1747-2015 Class II Terminated
FDA device recall Z-1747-2015 was initiated by Becton Dickinson & Co. on Nov 21, 2014 and is designated Class II. Reason for recall: The products may exhibit indications of excessive oxidation. Excessive oxidation may affect the viability of anaerobic microorganisms. The recall status is terminated (terminated Jan 7, 2016). Affected quantity: 92,710 units.
Recall Details
- Product Type
- Devices
- Report Date
- Jun 17, 2015
- Initiation Date
- Nov 21, 2014
- Termination Date
- Jan 7, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 92,710 units
Product Description
BBL Port A Cul tubes with Swabs Sterile Pack, catalog number 221607. For patient sample collection.
Reason for Recall
The products may exhibit indications of excessive oxidation. Excessive oxidation may affect the viability of anaerobic microorganisms.
Distribution Pattern
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.
Code Information
Part/Cat No. Lot / Serial No.Date of Mfr Exp. Date 221607 4067181 3/19/2014 3/5/2015 221607 4083274 4/3/2014 3/20/2015 221607 4124706 5/9/2014 4/24/2015 221607 4127564 5/22/2014 5/1/2015 221607 4170891 7/8/2014 6/19/2015 221607 4006235 2/18/2014 12/26/2014 221607 4028420 2/19/2014 1/21/2015
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1747-2015
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026