Home › Device types › DQR
Cannula, Catheter
FDA product code DQR · Class 2 · Cardiovascular
195
Registered devices
654
Adverse events
26
Recalls
25
510(k) clearances
Devices with this code
Embosafe — ANGIODYNAMICS, INC.Arterial Cannula — SORIN GROUP ITALIA SRLV. Mueller — CAREFUSION 2200, INCArterial Cannula — SORIN GROUP ITALIA SRLArterial Cannula — SORIN GROUP ITALIA SRLAngioDynamics — ANGIODYNAMICS, INC.Arterial Cannula — SORIN GROUP ITALIA SRLAngioDynamics — ANGIODYNAMICS, INC.Micro Access — ANGIODYNAMICS, INC.AngioDynamics — ANGIODYNAMICS, INC.enableCV OptiSite™ Arterial Perfusion Cannula — ENABLECV INC.AngioDynamics — ANGIODYNAMICS, INC.AngioDynamics — ANGIODYNAMICS, INC.AngioDynamics — ANGIODYNAMICS, INC.Arterial Perfusion Cannula — Edwards Lifesciences LLCArterial Cannula — SORIN GROUP ITALIA SRLArterial Cannula — SORIN GROUP ITALIA SRLCook — COOK INCORPORATEDArterial Cannula — SORIN GROUP ITALIA SRLArterial Cannula — SORIN GROUP ITALIA SRLAngioDynamics — ANGIODYNAMICS, INC.AngioDynamics — ANGIODYNAMICS, INC.Arterial Cannula — SORIN GROUP ITALIA SRLAngioDynamics — ANGIODYNAMICS, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-05-14 | Edwards Lifesciences, LLC | due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body. |
| 2025-05-14 | Edwards Lifesciences, LLC | due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body. |
| 2025-05-14 | Edwards Lifesciences, LLC | due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body. |
| 2025-05-14 | Edwards Lifesciences, LLC | due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body. |
| 2025-05-14 | Edwards Lifesciences, LLC | due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body. |
| 2025-05-14 | Edwards Lifesciences, LLC | due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body. |
| 2020-10-14 | Angiodynamics, Inc. | 5F Micro-Introducer Kits may not contain the correct device, packaged with a 4F Sheath/Dilator component |
| 2018-03-07 | SPS Sterilization, Inc | The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the |
| 2013-04-30 | Angiodynamics, Inc. | AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT NeverTouch Procedure Kits, because the potential exists that the micro Introducer (shea |
| 2004-03-11 | Guidant Corp-Cpi Division | The terminal hub component in a some of the catheters has an unintended abrupt transition between the entry port and the catheter lumen which can result in di |
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