FDAFDA · Food and drugs·Recall number Z-0932-2013
Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation.
Published March 20, 2013 · Recall initiated: August 24, 2012
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
Implants were incorrectly laser marked as 23mm instead of 28mm.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Spine Smith Partners LP
- Distributor
- Distributed in Texas.
- Lot
- Part Number: 0609-2809-06, Lot: 39AQ
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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