FDAFDA · Food and drugs·Recall number Z-2412-2023
Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only
Published August 23, 2023 · Recall initiated: June 28, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Product labeling contains incorrect expiration date
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Medtronic Neurosurgery
- Distributor
- US Nationwide distribution in the states of NJ, FL, CA, IL.
- Lot
- Lot # 226632942; UDI-DI: 00763000624781
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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