TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)
Class I - DangerousWhat Should You Do?
- Check if you have this product: model number NMRM6122 lot number 16E03727 16E05728 model number NMRM6133 lot number 16E02726 16E09730
- 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:
- TYRX Inc.
- Reason for Recall:
- TRYX products are being recalled since the processes of spaying, welding, drying oven and polymer were not adequately validated.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)
Product Codes/Lot Numbers:
model number NMRM6122 lot number 16E03727 16E05728 model number NMRM6133 lot number 16E02726 16E09730
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2541-2016
Related Recalls
TRYX products are being recalled since the processes of spaying, welding, drying oven and polymer were not adequately validated.
TRYX products are being recalled since the processes of spaying, welding, drying oven and polymer were not adequately validated.