Home › Device types › QBP
Cap, Device Disinfectant
FDA product code QBP · Class 2 · General Hospital
15
Registered devices
24
Adverse events
2
Recalls
22
510(k) clearances
Devices with this code
McKesson — MCKESSON MEDICAL-SURGICAL INC.McKesson — MCKESSON MEDICAL-SURGICAL INC.SwabTip™ — ICU MEDICAL, INC.BD PureHub — BECTON, DICKINSON AND COMPANYDualCap® — Merit Medical Systems, Inc.DualCap® — Merit Medical Systems, Inc.BD PureHub — BECTON, DICKINSON AND COMPANYSwabSleeve™ — ICU MEDICAL, INC.DualCap® — Merit Medical Systems, Inc.DualCap® — Merit Medical Systems, Inc.DualCap® — Merit Medical Systems, Inc.DualCap® — Merit Medical Systems, Inc.SwabCap™ — ICU MEDICAL, INC.SwabCap™ — ICU MEDICAL, INC.DualCap® — Merit Medical Systems, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-06-16 | MEDLINE INDUSTRIES, LP - Northfield | SwabFlush syringes are affected by the ICU Medical recall of their SwabCap Disinfecting Cap due to a manufacturing issue which affects the seal between the foil |
| 2025-06-03 | ICU Medical, Inc. | Due to a manufacturing issue, disinfecting cap for needle-free connectors may have an incomplete seal between the foil lid and plastic container, which may resu |
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