🔍 RecallPedia

BD Multi Check CD4 Low Control Catalog No. 340916 is intended as a complete process control for immunophenotyping by flow cytometry.

Class I - Dangerous
🏥 Medical Devices Recalled: July 18, 2014 BD Biosciences, Systems & Reagents Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Catalog number 340916; Lot number BM084L
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
BD Biosciences, Systems & Reagents
Reason for Recall:
The outer box label contains the incorrect distribution date: Box states 2017-09-02 ; should be 2014-09-02
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

BD Multi Check CD4 Low Control Catalog No. 340916 is intended as a complete process control for immunophenotyping by flow cytometry.

Product Codes/Lot Numbers:

Catalog number 340916; Lot number BM084L

Distribution:

Distributed in: IN, MA, TX, VA, KY, MD, PA, GA, BD

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2233-2014

Related Recalls

BD Flow Cytometers; used on all BD FACSCount, BD FACSCalibur, BD FACSCanto, BD FACSCanto II, BD LSR II, BD LSRFortessa,BD FACSAria, BD FACSAria II, BD FACSAria Ill, BD lnflux, BD FACSArray,BD Pathway 855, BD Pathway 435 and all SORP instruments. BD Biosciences Flow cytometers for the enumeration of tissue and biological fluid samples such as blood and blood components.

BD Biosciences, Systems & Reagents

Class I - Dangerous

Instruments installed between June 2007 and September 2011 do not contain labeling pursuant to the Food and Drug Administration's (FDA's) Guidance on Laser Products- Conformance with IEC 60825-1 and IEC 60601-2-22 (Laser Notice No. 50).

Jun 15, 2015 Diagnostic Equipment Nationwide View Details →