Becton Dickinson
6 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Becton Dickinson and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-05-27FDA-DeviceClass IIBecton Dickinson Swan-Ganz catheter recalled for hub leak risk
Catheters 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.
- 2026-05-27FDA-DeviceClass IIBecton Dickinson Swan-Ganz Jr Catheter recalled for leak risk
Catheters 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.
- 2026-05-27FDA-DeviceClass IIBecton Dickinson Swan-Ganz catheters recalled for leak risk
Catheters 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.
- 2026-03-18FDA-DeviceClass IICheck BD syringes for packaging error
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
- 2025-11-26FDA-DeviceClass IIBD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.
- 2025-11-19FDA-DeviceClass IIBD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument enters an error state and the cuvettes cannot be used.
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