RecallRadar

FDA Device recall Z-3187-2026

REF:B5ST Ethicon Endo-Surgery, Inc

On 2026-09-23 the FDA classified a Class II recall of REF:B5ST 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-3187-2026
ClassificationClass II
Statusongoing
Initiated2026-08-19
Published2026-09-23
Last updated2026-09-29 05:30 UTC
CompanyStryker Sustainability Solutions
DistributionUS

Product

REF:B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 5X75MM

Reason

Reusable access port system may crack or seperate during use.

Identifiers

code_info
UDI:(01)00885825014254/ Lots: 16028740 16083100 16098933 16106547 16130667 16160384 16160418 16160460 16181332…UDI:(01)00885825014254/ Lots: 16028740 16083100 16098933 16106547 16130667 16160384 16160418 16160460 16181332 16201793 16207031 16234052 16264116 16418941 16421915 16422882 16476685 16493231 16948345 16954673 16977948 16993151 17151380 17160201 17210355 17239624 17271015 17271027 17324927 17341521 17342144 17378894 17412852 17426084 17457260 17491569 17499741 17512459 17521310 17526338

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-3187-2026%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.