FDA Medical devices recall ·
COOK MEDICAL Cook Staged Extubation Set: Reference Part Number… recall
- Recall number
- Z-1782-2026
- Date
- (initiated March 5, 2026)
- Company / brand
- Cook Incorporated
750 N Daniels Way, Bloomington, IN, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 95 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
COOK MEDICAL Cook Staged Extubation Set: Reference Part Number C-CAE-14.0-83-EXTU, Order Number G24073
Why was it recalled?
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Reference Part Number C-CAE-14.0-83-EXTU, UDI (01)00827002240735(17)270509(10)16010654, Lot Number 16010654.
Distribution
Worldwide distribution.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1782-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.