RecallRadar

FDA Device recall Z-2082-2025

Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016A Software Version: N/A Product Description: T…

On 2025-07-16 the FDA classified a Class I recall of Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016A Software Version: N/A Product Description: T… by Edwards Lifesciences, citing due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2082-2025
ClassificationClass I
Statusongoing
Initiated2025-05-14
Published2025-07-16
Last updated2026-09-13 11:57 UTC
CompanyEdwards Lifesciences
DistributionUS

Product

Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours. Component: No

Reason

due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.

Identifiers

code_info
Lot Code: Model No: FEMII016A; UDI: 00690103031232; All lots up to: BSLC8179 Serial Numbers: 130544 130757 131105 13131…Lot Code: Model No: FEMII016A; UDI: 00690103031232; All lots up to: BSLC8179 Serial Numbers: 130544 130757 131105 131313 131511 131535 131888 131925 132504 BSLC0184 BSLC0386 BSLC0596 BSLC1311 BSLC3741 BSLC4162 BSLC5040 BSLC6487 BSLC8179

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2082-2025%22

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