Home › Device types › DQX
Wire, Guide, Catheter
FDA product code DQX · Class 2 · Cardiovascular
5,833
Registered devices
33,688
Adverse events
258
Recalls
766
510(k) clearances
Devices with this code
STABILIZER — CORDIS CORPORATIONARROW — TELEFLEX INCORPORATEDHalberd18 — ASAHI INTECC CO., LTD.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.CONFIANZA PRO 8-20 190cm Pre-shape — ASAHI INTECC CO., LTD.Guidewire — GALT MEDICAL CORP.ARROW — TELEFLEX INCORPORATEDCook — COOK INCORPORATEDMcNamara — COOK INCORPORATEDNavilyst — NAVILYST MEDICAL, INC.Amplatz — COOK INCORPORATEDARROW — TELEFLEX INCORPORATEDInQwire® — Merit Medical Systems, Inc.ARROW — TELEFLEX INCORPORATEDAmplatz — COOK INCORPORATEDGuidewire — ARGON MEDICAL DEVICES, INC.Magic Torque™ — BOSTON SCIENTIFIC CORPORATIONSunmed Guide Wires — Sunny Medical Device (Shenzhen) Co., Ltd.ARROW — TELEFLEX INCORPORATEDEMERALD — Cordis US Corp.ARROW — TELEFLEX INCORPORATEDGuidewire — ARGON MEDICAL DEVICES, INC.InQwire® — Merit Medical Systems, Inc.Cook — COOK INCORPORATED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-06-26 | Galt Medical Corporation | Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits. |
| 2026-05-08 | Merit Medical Systems, Inc. | Due to unsealed portions of pouches. |
| 2026-04-21 | ARROW INTERNATIONAL, LLC | Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality iss |
| 2026-03-05 | Cook Incorporated | Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. |
| 2026-03-05 | Cook Incorporated | Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. |
| 2026-03-05 | Cook Incorporated | Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. |
| 2026-02-25 | Medline Industries, LP | The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. |
| 2025-03-27 | Galt Medical Corporation | Due to a potential open seal in the sterile barrier packaging. |
| 2024-10-14 | Cook Incorporated | Devices from the affected device lots have labels that state the incorrect expiration dates. |
| 2024-10-08 | Cook Incorporated | Affected device lots have labels that state the incorrect expiration dates. |
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