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[Recalled] DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures. — The sterile blister packaging may be damaged, and sterility may be compromised | FDA 2024-01-09

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

ProductDISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.
Brand / manufacturerAesculap Inc
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1244-2024
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date09 January 2024
EAN / barcode04046963620455

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: The sterile blister packaging may be damaged, and sterility may be compromised.

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 Aesculap Inc

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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