T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient use, non-sterile prescription device designed for use in a hospital or home care environment.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot No. 083115, 090715, and 122815
- 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:
- Reports that the T-piece does not fit on the nebulizer.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient use, non-sterile prescription device designed for use in a hospital or home care environment.
Product Codes/Lot Numbers:
Lot No. 083115, 090715, and 122815
Distribution:
Distributed in: TX, NY, PA, TN, SC, OH
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0796-2016
Related Recalls
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.
It has been determined that three lots of model number 4515-15-25 CO2 Sample Line 15' tube, male Luer lock connectors may contain a 30' tube instead of the 15' length.