FDA Device recall Z-0701-2013
Becton, Dickinson and Company, BD MAX (tm) (6 channel) Instruments, Catalog number 441916, clinical diagnostic instrument
- FDA Device
- Class II
- terminated
- Published 2013-01-30
On 2013-01-30 the FDA classified a Class II recall of Becton, Dickinson and Company, BD MAX (tm) (6 channel) Instruments, Catalog number 441916, clinical diagnostic instrument by Becton Dickinson And, citing clinical diagnostic instrument may exhibit minor defects, which could lead to erroneous test results.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0701-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-09-18 |
| Published | 2013-01-30 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Becton Dickinson And |
| Distribution | CT, FL, IL, KS, MD, MI, MO, NY, PA, RI, TX, WI |
Product
Becton, Dickinson and Company, BD MAX (tm) (6 channel) Instruments, Catalog number 441916, clinical diagnostic instrument.
Reason
Clinical diagnostic instrument may exhibit minor defects, which could lead to erroneous test results.
Identifiers
| code_info | Serial Numbers: MX0001 to MX0065 CM0001 to CM0105 NOTE: Serial numbers are assigned sequentially. The above r…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. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0701-2013%22
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