FDA Medical devices recall ·
INCA (Infant Nasal Cannulae Assy) Neonatal Nasal CPAP, Replacement Set recall
This is an FDA Class I recall — the most serious type.
- Recall number
- Z-3140-2026
- Date
- (initiated August 11, 2026)
- Company / brand
- CooperSurgical, Inc.
95 Corporate Dr, Trumbull, CT, United States - Category
- Medical devices › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 149 boxes (745 units)
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
INCA (Infant Nasal Cannulae Assy) Neonatal Nasal CPAP, Replacement Set. Stay-Flex tubing component. 5 units per box. Model Numbers: 44-0712, 44-0707, 44-0709, 44-0715.
Why was it recalled?
Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP pressure, possibly reducing the effectiveness of treatment and lead to decreased oxygenation until connection is restored.
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
1. Model Number: 44-0712. UDI-DI: (01)60888937009516. Lot Code: 550031624. 2. Model Number: 44-0707. UDI-DI: (01)20888937009488. Lot Code: 550021057. 3. Model Number: 44-0709. UDI-DI: (01)20888937009495. Lot Code: 550031623. 4. Model Number: 44-0715. UDI-DI: (01)20888937009525. Lot Code: 550031625.
Distribution
Nationwide distribution to CT, FL, GA, IA, IL, IN, MD, MI, MS, NJ, NY, OH, PA, VA. International distribution to Brazil and Peru.
States: Connecticut Florida Georgia Iowa Illinois Indiana Maryland Michigan Mississippi New Jersey New York Ohio Pennsylvania Virginia
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (medical devices), recall Z-3140-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.