FDA Device Intelligence
Home › Device types › FPK

Tubing, Fluid Delivery

FDA product code FPK · Class 2 · General Hospital

345
Registered devices
850
Adverse events
28
Recalls
64
510(k) clearances

Devices with this code

Pressure Monitor Tubing — Merit Medical Systems, Inc.MEDRAD® Twist & Go Sterile High Pressure Connector Tubing, 75cm (30in) — BAYER MEDICAL CARE INC.High Pressure Tubing — Merit Medical Systems, Inc.High Pressure Tubing — Merit Medical Systems, Inc.Pressure Monitor Tubing — Merit Medical Systems, Inc.25ft/7.6m IV Ext Set w/ Sleeve — QUEST MEDICAL INCMedex — ICU MEDICAL, INC.High Pressure Tubing, Keep™ — Merit Medical Systems, Inc.High Pressure Tubing — Merit Medical Systems, Inc.MEDRAD® Twist & Go Sterile High Pressure Connector Tubing, 120cm (48in) — BAYER MEDICAL CARE INC.VYGON — Vygon CorporationHigh Pressure Tubing — Merit Medical Systems, Inc.Exoflex 10.5in. T-Extension Set — QUEST MEDICAL INCEcoFLX™ — DOUGLAS MEDICAL PRODUCTS, INC.Medex — ICU MEDICAL, INC.MiniMed™ Duo™ Infusion Tubing — Unomedical A/SVYGON — Vygon CorporationHigh Pressure Tubing — Merit Medical Systems, Inc.Pressure Monitor Tubing — Merit Medical Systems, Inc.Pressure Monitor Tubing — Merit Medical Systems, Inc.FLEBOSET — LABORATORIOS GRIFOLS SAVYGON — Vygon CorporationMEDRAD® Twist & Go Disposable Syringe 150 mL with Quick Fill Tube — BAYER MEDICAL CARE INC.VYGON — Vygon Corporation

Recent recalls

DateFirmReason
2025-06-05Merit Medical Systems, Inc.High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affec
2017-09-10Medtronic Inc.Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
2013-02-19Hospira Inc.Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore Extension Set, 59 inch with Spin Lock Collar, Non-DEHP, identified above due to a conf
2012-05-18MOOG Medical Devices GroupMoog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could rev
2012-05-18MOOG Medical Devices GroupMoog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could rev
2012-05-18MOOG Medical Devices GroupMoog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could rev
2012-05-18MOOG Medical Devices GroupMoog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could rev
2012-05-18MOOG Medical Devices GroupMoog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could rev
2012-05-18MOOG Medical Devices GroupMoog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could rev
2012-05-18MOOG Medical Devices GroupMoog Medical Device Group became aware on March 23, 2011 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could rev

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.