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[Recalled] Merit Medical, REF: R2007, EsophyX Z+, (1) Fastener Delivery Device, SterileEO, RxOnly — Update to IFU to provide additional information related to risk with device ove… | FDA 2025-03-14

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

ProductMerit Medical, REF: R2007, EsophyX Z+, (1) Fastener Delivery Device, SterileEO, RxOnly
Brand / manufacturerMerit Medical Systems, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1640-2025
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date14 March 2025
EAN / barcode00810275011089

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Update to IFU to provide additional information related to risk with device over-rotation and multiple deployment of fasteners.

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 Merit Medical Systems, 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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