[Recalled] MATResponder Tourniquet; Catalog number MATR: UPC 78353 00008; MATCombat Tourniquet, Catalog number MATC; UPC 78353 00010; MATResponder Tourniquet and MATCombat Tourniquet are essentially the same product with different color
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | MATResponder Tourniquet; Catalog number MATR: UPC 78353 00008; MATCombat Tourniquet, Catalog number MATC; UPC 78353 00010; MATResponder Tourniquet and MATCombat Tourniquet are essentially the same product with different color schemes manual nonpneumatic tourniquet devices. The device provides |
|---|---|
| Brand / manufacturer | Pyng Medical Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0228-2016 |
| Country of notice | Canada |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 31 August 2015 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Once tested, it is required that the tourniquet be returned to its Ready position then placed in its packaging. Each tourniquet was tested for functionality, but in some cases, the tourniquet was not returned to its Ready position prior to packaging.
This Class II recall concerns device products distributed in Canada 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 →
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.