Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7 ft, oxygen tube, 7 ft. CO2 tube RX only.For Single Patient Use only. Distributed by Tri-Anium Assembled in Mexico. Usage: Delivery of Anesthesia.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Salter Part Number SO-1296, Tri-Anium Part numaber: 301-P3600; Lot number: 032612.
- 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:
- SALTER LABS
- Reason for Recall:
- A complaint was received, and later verified, that product labeled as SO-1296 with male luer lock connector actually contained product with a female luer lock connector.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7 ft, oxygen tube, 7 ft. CO2 tube RX only.For Single Patient Use only. Distributed by Tri-Anium Assembled in Mexico. Usage: Delivery of Anesthesia.
Product Codes/Lot Numbers:
Salter Part Number SO-1296, Tri-Anium Part numaber: 301-P3600; Lot number: 032612.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1898-2012
Related Recalls
Reports that the T-piece does not fit on the nebulizer.
The Inspiratory valve cap on the nebulizer reservoir tower may be loose and may detach before or during treatment.
The case label correctly states partial rebreather but the insert label incorrectly states non-rebreather.