BECTON, DICKINSON AND COMPANY
2 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (2)
Devices registered here (1)
- Computer, Diagnostic, ProgrammableProduct code DQK (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.1425
Recalls & enforcement
- Class IIOngoing2026-08-11Due to incorrect switching of Channel 1 and 2 on the module and flag labels on the tissue oximetry cables.
- Class IIOngoing2026-04-08Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
Related
- All facilities operated by Becton, Dickinson and Company
- EDWARDS LIFESCIENCES TECHNOLOGY SARL (PR)
- CCT Critical Care Technologies, S.R.L. Also Trading As Edwards Lifesciences AG (DO)
- Edwards Lifesciences Holding B.V. (NL)
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “BECTON, DICKINSON AND COMPANY (FEI 3032916632) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3032916632-becton-dickinson-and-company/
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