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Cook Medical Recall: Cook Staged Extubation Set Labeled with Expired Dates in 2026 Class II Recall

Cook Medical issued a global recall of 95 units of the Cook Staged Extubation Set due to expiration dates that exceed true shelf life. The affected lots carry Reference Part Number C-CAE-14.0-83-EXTU and Order Number G24073. The recall is classified as HIGH hazard. Patients and healthcare providers should stop using the device immediately and follow recall instructions from Cook Incorporated.

Official notice
CookHealth & Personal CareMedical DevicesReference Part Number C-CAE-14.0-83-EXTUUDI (01)00827002240735(17)270509(10)16010654Lot Number 16010654.

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
March 5, 2026
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
March 5, 2026
Hazard Level
HIGH
Brand
Cook
Category
Health & Personal Care
Sold At
Unknown
At-Risk Groups
GENERAL, PREGNANT, PREGNANT

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Cook
Product type
Staged Extubation Set
Model numbers
Reference Part Number C-CAE-14.0-83-EXTU, UDI (01)00827002240735(17)270509(10)16010654, Lot Number 16010654.
Sold at
Unknown

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    March 5, 2026

  2. Reported by FDA DEVICE

    April 15, 2026

  3. RecallRadar source check

    April 22, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Cook Incorporated or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

About This Product

The Cook Staged Extubation Set is a medical device used in airway management procedures. It is typically used by healthcare professionals during extubation steps.

Why This Is Dangerous

The hazard stems from expiration dates that exceed true shelf life, potentially affecting sterility or device performance.

Industry Context

This recall is not described as part of a broader pattern in the provided data.

Real-World Impact

Immediate device discontinuation required. Potential impact on patient safety if used past shelf life.

Practical Guidance

How to identify if yours is affected

  1. Check Reference Part Number C-CAE-14.0-83-EXTU
  2. Verify Order Number G24073
  3. Check Lot Number 16010654

Where to find product info

Refer to FDA recall listing and Cook’s recall communications

What timeline to expect

Manufacturer guidance will provide timelines for replacement or remediation; typical timelines vary by facility

If the manufacturer is unresponsive

  • Escalate to hospital risk management or infection control
  • Contact FDA MedWatch if manufacturer is unresponsive

How to prevent similar issues

  • Verify shelf life and labeling before procurement
  • Maintain strict inventory controls for medical devices
  • Adopt standard recalls monitoring for medical devices

Documentation advice

Keep recall notices, UDI, lot numbers, correspondence, and replacement records

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Product Details

Brand: Cook. Product: Cook Staged Extubation Set. Reference Part Number: C-CAE-14.0-83-EXTU. Order Number: G24073. Quantity: 95 units. Distribution: Worldwide.

Reported Incidents

No specific injuries or incidents are described in the provided data.

Key Facts

  • Reference Part Number C-CAE-14.0-83-EXTU

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTPREGNANTPREGNANTPETS
Injury Types
OTHERELECTRICALPOISONINGFALL

Product Details

Brand
Model Numbers
Reference Part Number C-CAE-14.0-83-EXTU
UDI (01)00827002240735(17)270509(10)16010654
Lot Number 16010654.
Report Date
April 15, 2026
Recall Status
ACTIVE

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