DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide assistance in both the planning (pre-operative) and the surgical (intra-operative) phases of dental implantation surgery.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Work Order (lot): 1619 and 1620
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Neocis Inc.
- Reason for Recall:
- The LRUL and LLUR posterior chairside splints and LLUR anterior chairside splints may be mislabeled.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide assistance in both the planning (pre-operative) and the surgical (intra-operative) phases of dental implantation surgery.
Product Codes/Lot Numbers:
Work Order (lot): 1619 and 1620
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2637-2020
Related Recalls
The LRUL and LLUR posterior chairside splints and the LLUR anterior chairside splints may be mislabeled.
The LRUL and LLUR posterior chairside splints and LLUR anterior chairside splints may be mislabeled.
The LRUL and LLUR posterior chairside splints and LLUR anterior chairside splints may be mislabeled.