FDAFDA · Food and drugs·Recall number Z-1071-2020
Centurion- Driveline System Kit TRIDM250 OUTPATIENT DRIVELINE MGMT SYSTEM
Published February 12, 2020 · Recall initiated: December 11, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Incomplete seals on the sterile package may compromise the sterility
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Centurion Medical Products Corporation
- Distributor
- Nationwide Foreign: GHANA
- Lot
- TRIDM250 OUTPATIENT DRIVELINE MGMT SYSTEM 2019012890
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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