Home › Device types › FOZ
Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
FDA product code FOZ · Class 2 · General Hospital
5,364
Registered devices
48,998
Adverse events
394
Recalls
507
510(k) clearances
Devices with this code
ARROW — TELEFLEX INCORPORATEDARROW — TELEFLEX INCORPORATEDJelco — ICU MEDICAL, INC.PowerGlide Pro — Bard Access Systems, Inc.ARROW — TELEFLEX INCORPORATEDMcKesson — MCKESSON MEDICAL-SURGICAL INC.Cook — COOK INCORPORATEDLuther Needlesafe Products — LUTHER NEEDLESAFE PRODUCTS, LLCNIPRO SAFELET CATH — NIPRO MEDICAL CORPORATIONEXEL Safelet Catheter — Exel InternationalINTROCAN SAFETY® — B. BRAUN MEDICAL INC.ARROW — TELEFLEX INCORPORATEDCragg McNamaraTM — Micro Therapeutics, Inc.First PICC™ S/L Peripherally Inserted Central Catheter Basic Kit — ARGON MEDICAL DEVICES, INC.Orion II — Health Line International CorporationARROW — TELEFLEX INCORPORATEDCook — COOK INCORPORATEDCook — COOK INCORPORATEDARROW — TELEFLEX INCORPORATEDARROW — TELEFLEX INCORPORATEDBD Nexiva — BECTON, DICKINSON AND COMPANYARROW — TELEFLEX INCORPORATEDARROW — TELEFLEX INCORPORATEDCook — COOK INCORPORATED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-11 | ARROW INTERNATIONAL, LLC | Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured |
| 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. |
| 2026-01-07 | Medline Industries, LP | Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated ster |
| 2026-01-07 | Medline Industries, LP | Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated ster |
| 2025-05-21 | Becton Dickinson Infusion Therapy Systems, Inc. | Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract. |
| 2025-05-21 | Becton Dickinson Infusion Therapy Systems, Inc. | Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract. |
| 2025-05-21 | Becton Dickinson Infusion Therapy Systems, Inc. | Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract. |
| 2025-05-21 | Becton Dickinson Infusion Therapy Systems, Inc. | Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract. |
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