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[Recalled] Curved Intraluminal Staplers, 21 mm diameter, Model CDH21A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen.

recall fda device united-states

Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.

Recall details

ProductCurved Intraluminal Staplers, 21 mm diameter, Model CDH21A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the anvil shaft in a locat
Brand / manufacturerEthicon Endo-Surgery Inc
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1267-2019
Country of noticeUnited States
Risk levelClass I
Hazard typerecall
Notice date11 April 2019

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: The staplers may have an insufficient firing stroke to break the washer and completely form staples.

This Class I 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

Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).

Read the full official notice →

Related recalls from Ethicon Endo-Surgery 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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