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MiniMed™ Duo™ Infusion Tubing
Unomedical A/S · Model 5082076-003 · UDI-DI 05705244005259
FPK
Prescription
10
510(k) clearances
850
Adverse events (5 deaths)
28
Recalls
65
Facilities
Description
Single use infusion tubing for subcutaneous infusion. The infusion tubing must be used as described in the Instruction for Use.
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 |
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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.