Becton Dickinson & Co.: Medical Device Recall in 2013 - (Recall #: Z-0701-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Becton, Dickinson and Company, BD MAX (tm) (6 channel) Instruments, Catalog number 441916, clinical diagnostic instrument.

Product Classification:

Class II

Date Initiated: September 18, 2012

Date Posted: January 30, 2013

Recall Number: Z-0701-2013

Event ID: 63949

Reason for Recall:

Clinical diagnostic instrument may exhibit minor defects, which could lead to erroneous test results.

Status: Terminated

Product Quantity: 86 Instruments

Code Information:

Serial Numbers: MX0001 to MX0065 CM0001 to CM0105 NOTE: Serial numbers are assigned sequentially. The above ranges will include all sequential numbers in between the beginning and end points.

Distribution Pattern:

USA including CT, FL, IL, KS, MD, MI, MO, NY, PA, RI, TX and WI. Internationally to Canada, Europe and Japan.

Voluntary or Mandated:

Voluntary: Firm initiated