[Recalled] URINE COLLECTION VHC, SKU DYLAB1016; Component No. 503581 — Specimen container included in kits is labeled as sterile, but has been identif… | FDA 2024-10-23
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | URINE COLLECTION VHC, SKU DYLAB1016; Component No. 503581 |
|---|---|
| Brand / manufacturer | MEDLINE INDUSTRIES, LP - Northfield |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0359-2025 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 23 October 2024 |
| EAN / barcode | 40195327139941 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Specimen container included in kits is labeled as sterile, but has been identified to be non-sterile. Long-term consequences may include unnecessary treatment and/or prolonged hospitalization.
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 MEDLINE INDUSTRIES, LP - Northfield
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.