Becton Dickinson Recalls BBL Port A Cul Tubes Due to Oxidation
Becton Dickinson is recalling BBL Port A Cul tubes because excessive oxidation may affect the viability of anaerobic microorganisms.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II. The hazard involves potential reduced viability of microorganisms due to oxidation, which is a functional defect rather than a direct physical injury or high-risk pathogen exposure, fitting the Moderate criteria for low-risk contamination or functional issues without reported illness.
Plain-English summary
Becton Dickinson & Co. is recalling BBL Port A Cul tubes, catalog number 221606. These are patient sample collection tubes containing a reduced transport medium intended to maintain the viability of anaerobic, facultative, and aerobic microorganisms during transport from the patient to the laboratory.
The recall is due to the possibility that the products may exhibit indications of excessive oxidation. This excessive oxidation may affect the viability of anaerobic microorganisms.
The affected products were distributed nationwide in the United States, including 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. The total quantity involved is 145,860 tubes. Specific lot numbers and expiration dates are listed in the agency's recall record.
The recalled product
- Product
- BBL Port A Cul tubes, catalog number 221606. Patient sample collection tubes. BBL Port A Cul tubes, jars and vials contain a reduced transport medium and are intended to maintain the viability of anaerobic, facultative and aerobic microorganisms during transport from the patient
- Manufacturer
- Becton Dickinson & Co.
- Affected units
- 145,860
Distribution
Part of a larger recall action
This product is one of 2 recalled by Becton Dickinson & Co. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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