FDAFDA · Food and drugs·Recall number Z-1239-2017
Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701
Published March 1, 2017 · Recall initiated: February 2, 2017
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
The single use devices are provided sterile and do not have an expiration date on the label.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Smith & Nephew, Inc.
- Distributor
- Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela
- Lot
- Batch Numbers: 50586138 50458123 50418120 50339534 50306882 50285907 50248565 50231427 50197615 50171397 50158655 50138049 50119457 50089297 50082581 50069485
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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