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FDA · Medical devices ·

REF:B5LT Ethicon Endo-Surgery recall

Stryker Sustainability Solutions recalled REF:B5LT Ethicon Endo-Surgery on September 23, 2026 because of reusable access port system may crack or seperate during use. It was sold nationwide.

Why it was recalled

Reusable access port system may crack or seperate during use.

What's recalled

REF:B5LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 5X100MM

Quantity: 205,704 units

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Stryker Sustainability Solutions, Tempe, AZ
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
US Nationwide distribution including in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Mi…
Status
Ongoing
Recall number
Z-3186-2026
Source
U.S. Food and Drug Administration

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