[Recalled] CRANIOTOMY PACK, Pack Number DYNJ46552O — A non-sterile Mastisol component, which was not labeled as being sterile or non… | FDA 2024-06-18
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | CRANIOTOMY PACK, Pack Number DYNJ46552O |
|---|---|
| Brand / manufacturer | MEDLINE INDUSTRIES, LP - Northfield |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-3069-2024 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 18 June 2024 |
| EAN / barcode | 40195327467044 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
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.