FDAFDA · Food and drugs·Recall number Z-2342-2018
Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery
Published July 11, 2018 · Recall initiated: May 14, 2018
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
Blades are loose in handles and may fall out due to non cured epoxy
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Beaver Visitec
- Distributor
- US Nationwide in the states of CA, IA, CO, HI, IA, MD & TX
- Lot
- Lot Numbers: 6002436 & 6002663
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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