RecallRadar

FDA Device recall Z-3183-2026

REF:2B5ST Ethicon Endo-Surgery, Inc

On 2026-09-23 the FDA classified a Class II recall of REF:2B5ST Ethicon Endo-Surgery, Inc by Stryker Sustainability Solutions, citing reusable access port system may crack or seperate during use.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-3183-2026
ClassificationClass II
Statusongoing
Initiated2026-08-19
Published2026-09-23
Last updated2026-09-29 05:30 UTC
CompanyStryker Sustainability Solutions
DistributionUS

Product

REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM

Reason

Reusable access port system may crack or seperate during use.

Identifiers

code_info
UDI: (01)00885825017231/ Lots: 16188647 16210212 16243934 16267300 16285639 16285656 16306188 16306231 16364978…UDI: (01)00885825017231/ Lots: 16188647 16210212 16243934 16267300 16285639 16285656 16306188 16306231 16364978 16470903 16521533 16547722 16580202 16599810 16637989 16656930 16665550 17005619 17069758 17113276 17117460 17146892 17172722 17389157

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-29 05:30 UTC. Current status: ongoing.

Other recalls by Stryker Sustainability Solutions

All Stryker Sustainability Solutions recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3183-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.