[Recalled] PROTEXIS Latex Micro Surgical Gloves Size 8.0 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protectio
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | PROTEXIS Latex Micro Surgical Gloves Size 8.0 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for sensitivity or durability d |
|---|---|
| Brand / manufacturer | Cardinal Health 200, LLC |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2917-2020 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 29 July 2020 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
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.