[Recalled] Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is an extruded tube used as an extension for different types of devices in an operating room, bonded with 2 female sure grip connectors at each end of the tub
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is an extruded tube used as an extension for different types of devices in an operating room, bonded with 2 female sure grip connectors at each end of the tube to facilitate the plug/ insertion of the device and also includes a m |
|---|---|
| Brand / manufacturer | Medtronic Minimally Invasive Therapies Group |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0936-2018 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 24 October 2017 |
| EAN / barcode | 8888301515 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Incorrect packaging. In one lot of Argyle Suction Tubing, the pouch may be incorrectly labeled as the Salem Sump Dual Lumen Stomach Tube. This product may have been distributed within the case of Argyle Suction Tubing.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Medtronic Minimally Invasive Therapies Group
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.