Device recall
Cardinal Health Presource PBDS kits, Containing BD Alaris Pump Infusion Sets used with BD Alaris Pump Module Model 8100, labeled as: KIT EMERGENCY BASKET GENERAL, CATALOG # RES307732A
- Recall number
- Z-0222-2027
- Event id
- 100058
- Status
- Open, Classified
- FDA classification
- Class II
- Recalling firm
- Cardinal Health 200, LLC
- Posted
- Nov 2, 2026
- Initiated
- Sep 24, 2026
- Product code
- OKI
- Device type
- Emergency Response Safety Kit
- Reason
- Kits contain infusion sets which were recalled for performance issues.
- Root cause
- Nonconforming Material/Component
- Quantity
- 48 kits
- Code info
- GTIN 10195594772482 (ea) 50195594772480 (cs), Lot # 964798
- Distribution
- US and Canada
- Location
- Waukegan, IL