[Recalled] Henry Shein GLOVES, packaged in the following sizes and descriptions: a. Glove 6.5 Pack, 25 Pairs, 10 packs per case; b. Glove 7.0 Pack, 25 Pairs, 10 packs per case; c. Glove 7.5 Pack, 25 Pairs, 10 packs per case;
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Henry Shein GLOVES, packaged in the following sizes and descriptions: a. Glove 6.5 Pack, 25 Pairs, 10 packs per case; b. Glove 7.0 Pack, 25 Pairs, 10 packs per case; c. Glove 7.5 Pack, 25 Pairs, 10 packs per case; d. Glove 8.0 Pack, 25 Pairs, 10 packs per case; e. Glove 8.5 Pack, |
|---|---|
| Brand / manufacturer | Stradis Healthcare |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0934-2023 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 15 December 2022 |
| EAN / barcode | 222990332 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Potential for the outer bag having pinhole leaks near the seal, which may result in a breach in the sterility of the kit.
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 Stradis Healthcare
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.