[Recalled] ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only. — There have been repor
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only. |
|---|---|
| Brand / manufacturer | Medline Industries Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0058-2021 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 01 September 2020 |
| EAN / barcode | 06919010016 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: There have been reports of the suction catheter coming apart from the device assembly during use.
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 →
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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.