FDAFDA · Food and drugs·Recall number Z-1612-2013
Terumo Glidesheath (tm), 6 French, Nitinol wire, product code 15-1060. Used to facilitate placing a catheter through the skin into a vein or artery.
Published July 3, 2013 · Recall initiated: May 30, 2013
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
Medical devices were incorrectly labeled with extended expiration dates.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Terumo Medical Corporation
- Distributor
- Nationwide Distribution.
- Lot
- Lot MP08
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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