Recall Z-1780-2026— Cook Incorporated

Name: FDA recall Z-1780-2026
Creator: U.S. Food and Drug Administration
Published: 2026-03-05

Class II · Ongoing

Class II FDA medical device recall by Cook Incorporated, initiated 2026-03-05. It names one FDA 510(k) clearance: K193133. Product: COOK MEDICAL Blue Rhino¿ G2-Multi Percutaneous Tracheostomy Introducer Tray: Reference Part Number C-PTISY-100-HC-G-NA, Order Number G57703; Reference Part Number C-PTISY-100-UNL-HC-G-NA, Order Number G57706; Reference Part Number C-PTISY-100-UNS-HC-G-NA, Order Number G57704.. Reason: Products from the affected device lots were labeled with expiration dates that exceed the true shelf life..

Recalling firm: Cook Incorporated
Classification: Class II
Status: Ongoing
Initiated: 2026-03-05
Firm location: Bloomington, IN, United States

510(k) clearances named in this recall

1 on FDA's record

K193133 — Blue Rhino G1-Multi Percutaneous Tracheostomy Introducer Set, Blue Rhino G1-Multi Percutaneous Tracheostomy Introducer Tray, Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set, Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray, Weinmann-Multi Percutaneous Tracheostomy Exchange SetCook Incorporated·cleared 2019-12-12

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

COOK MEDICAL Blue Rhino¿ G2-Multi Percutaneous Tracheostomy Introducer Tray: Reference Part Number C-PTISY-100-HC-G-NA, Order Number G57703; Reference Part Number C-PTISY-100-UNL-HC-G-NA, Order Number G57706; Reference Part Number C-PTISY-100-UNS-HC-G-NA, Order Number G57704.

Reason for recall

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Data sourced from openFDA. This site is unofficial and independent of the FDA.