Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Dale Stabilock Endotracheal Tube Bolder 270 is a 2 piece device consisting of an adhesive base, Dale product number 273, that attaches to the patient's skin and a cushioned neckband with tube channel that attaches with hook & loop closures. The 270 is used to secure and stabilize endotracheal tubes, preventing unnecessary movement which can help prevent accidental .extubation
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot Numbers: 04 07 16 04, 08 16, 05 16 16
- 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:
- Dale Medical Products, Inc.
- Reason for Recall:
- ET Tube Holders contain an adhesive faceplate that may lose its adhesive properties and will not adhere to the patient's face.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Dale Stabilock Endotracheal Tube Bolder 270 is a 2 piece device consisting of an adhesive base, Dale product number 273, that attaches to the patient's skin and a cushioned neckband with tube channel that attaches with hook & loop closures. The 270 is used to secure and stabilize endotracheal tubes, preventing unnecessary movement which can help prevent accidental .extubation
Product Codes/Lot Numbers:
Lot Numbers: 04 07 16 04, 08 16, 05 16 16
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1928-2017
Related Recalls
ET Tube Holders contain an adhesive faceplate that may lose its adhesive properties and will not adhere to the patient's face.