Medline Industries, LP recalls Medline 14 Fr Suction Catheter Kits SKU DYND40972
- Recalling company
- Medline Industries, LP
- Product
- Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience kit
- Reason
- A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Dec 24, 2025
- Reported
- Feb 18, 2026
- Distribution
- Distribution US nationwide and Canada.
- Status
- Ongoing
- Quantity
- 141,971
- Lot / codes
- Kit lot 48625040001 UDI (ea) 10080196033317 UDI (case) 40080196033318¿
- Company location
- Northfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1312-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1312-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.