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[Recalled] Medline ROBOTIC-LF REF CDS984543B Lot 20AKA927 Expiration 2020-09-30 GTIN (01)10888277056350 — The sterile pack inside the Complete Delivery System (CDS) did not go through a… | FDA 2020-01-21

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 ROBOTIC-LF REF CDS984543B Lot 20AKA927 Expiration 2020-09-30 GTIN (01)10888277056350
Brand / manufacturerMedline Industries Inc
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1358-2020
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date21 January 2020
EAN / barcode10888277056350

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: The sterile pack inside the Complete Delivery System (CDS) did not go through a complete sterilization cycle, therefore the sterility of these components cannot be guaranteed.

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 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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