Kit BD Max Check-Points CPO IVD EU; Catalog # 278102
Reported: August 28, 2019 Initiated: July 17, 2019 #Z-2321-2019
Product Description
Kit BD Max Check-Points CPO IVD EU; Catalog # 278102
Reason for Recall
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Details
- Recalling Firm
- Becton Dickinson & Co.
- Units Affected
- 130 units
- Distribution
- AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, NH, NJ, NM, NV, NY, OH, OR, PA, PR, RI, SC, TN, TX, VA, WA, WI, WV Worldwide: Australia, Belgium, Brazil, Canada, Chile, China, Hong Kong, Japan, Korea, Mexico, Singapore, Taiwan
- Location
- Sparks, MD
Frequently Asked Questions
What product was recalled? ▼
Kit BD Max Check-Points CPO IVD EU; Catalog # 278102. Recalled by Becton Dickinson & Co.. Units affected: 130 units.
Why was this product recalled? ▼
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 28, 2019. Severity: Moderate. Recall number: Z-2321-2019.
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