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Serious recall: Injury is possible or has been reported. Take action promptly.

Becton, Dickinson and Company, BD Biosciences 2022-06-08 Health serious FDA
Health · FDA · Recall #FDA-Z-1215-2022

BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific reagent for the Anti-Kappa… Recall

Issued June 8, 2022 · Becton, Dickinson and Company, BD Biosciences

In June 2022, Becton, Dickinson and Company, BD Biosciences recalled the BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific reagent for the Anti-Kappa…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic flow profiles.

What you should do

  1. 1 Stop using BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific reagent for the Anti-Kappa… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Becton, Dickinson and Company, BD Biosciences to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Becton, Dickinson and Company, BD Biosciences
Category
Health
Recall date
June 8, 2022
Units affected
Not reported
Sold at
Worldwide distribution - US Nationwide distribution in the states of AL, CA, CO, DC, DE, FL, IA, IL, IN, LA, MA, MD, ME, MI, MN, MO, NC, ND,
Recall number
FDA-Z-1215-2022
Made in
United States
Issuing agency
FDA

In context

Read the official FDA notice

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