Home › Merit Medical Systems, Inc. › High Pressure Tubing
High Pressure Tubing
Merit Medical Systems, Inc. · Model D · UDI-DI 00884450821237
FPK
Prescription
10
510(k) clearances
850
Adverse events (5 deaths)
28
Recalls
65
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-06-05 | Merit 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 affected product may resu |
| 2017-09-10 | Medtronic Inc. | Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin. |
| 2013-02-19 | Hospira 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 confirmed customer repor |
| 2012-05-18 | MOOG Medical Devices Group | Moog Medical Device Group became aware on March 23, 2011 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu |
| 2012-05-18 | MOOG Medical Devices Group | Moog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu |
| 2012-05-18 | MOOG Medical Devices Group | Moog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu |
| 2012-05-18 | MOOG Medical Devices Group | Moog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu |
| 2012-05-18 | MOOG Medical Devices Group | Moog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu |
| 2012-05-18 | MOOG Medical Devices Group | Moog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu |
| 2012-05-18 | MOOG Medical Devices Group | Moog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu |
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 docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.