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[Recalled] Medline AMBULATORY MINI PACK, REF DYNJ82579; medical procedure convenience kit — It has been determined that certain Convenience kits that were packaged in brea… | FDA 2024-09-04

recall fda device united-states

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductMedline AMBULATORY MINI PACK, REF DYNJ82579; medical procedure convenience kit
Brand / manufacturerMEDLINE INDUSTRIES, LP - Northfield
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0172-2025
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date04 September 2024
EAN / barcode40195327198153

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.

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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