Becton, Dickinson and Company, BD MAX (tm) (6 channel) Instruments, Catalog number 441916, clinical diagnostic instrument.
Reported: January 30, 2013 Initiated: September 18, 2012 #Z-0701-2013
Product Description
Becton, Dickinson and Company, BD MAX (tm) (6 channel) Instruments, Catalog number 441916, clinical diagnostic instrument.
Reason for Recall
Clinical diagnostic instrument may exhibit minor defects, which could lead to erroneous test results.
Details
- Recalling Firm
- Becton Dickinson & Co.
- Units Affected
- 86 Instruments
- Distribution
- USA including CT, FL, IL, KS, MD, MI, MO, NY, PA, RI, TX and WI. Internationally to Canada, Europe and Japan.
- Location
- Sparks, MD
Frequently Asked Questions
What product was recalled? ▼
Becton, Dickinson and Company, BD MAX (tm) (6 channel) Instruments, Catalog number 441916, clinical diagnostic instrument.. Recalled by Becton Dickinson & Co.. Units affected: 86 Instruments.
Why was this product recalled? ▼
Clinical diagnostic instrument may exhibit minor defects, which could lead to erroneous test results.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 30, 2013. Severity: Moderate. Recall number: Z-0701-2013.
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