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[Recalled] CRANIOTOMY PACK, Pack Number DYNJ46552O — A non-sterile Mastisol component, which was not labeled as being sterile or non… | FDA 2024-06-18

recall fda device united-states

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

ProductCRANIOTOMY PACK, Pack Number DYNJ46552O
Brand / manufacturerMEDLINE INDUSTRIES, LP - Northfield
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-3069-2024
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date18 June 2024
EAN / barcode40195327467044

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 →

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.

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