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.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
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
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The Cook Staged Extubation Set is a medical device used in airway management procedures. It is typically used by healthcare professionals during extubation steps.
The hazard stems from expiration dates that exceed true shelf life, potentially affecting sterility or device performance.
This recall is not described as part of a broader pattern in the provided data.
Immediate device discontinuation required. Potential impact on patient safety if used past shelf life.
Refer to FDA recall listing and Cook’s recall communications
Manufacturer guidance will provide timelines for replacement or remediation; typical timelines vary by facility
Keep recall notices, UDI, lot numbers, correspondence, and replacement records
Brand: Cook. Product: Cook Staged Extubation Set. Reference Part Number: C-CAE-14.0-83-EXTU. Order Number: G24073. Quantity: 95 units. Distribution: Worldwide.
No specific injuries or incidents are described in the provided data.
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