Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access of a specimen from Catheter Port to BD Vacutainer¿ Blood Collection or Urine Collection Tubes.
Class I - Dangerous 🏥 Medical Devices
Recalled: August 2, 2021 Magnolia Medical Technologies Surgical Instruments
Nationwide
What Should You Do?
- Check if you have this product: Catalog #: 27BD-EN, Part #: P00165-000 Lot #9448037
- 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:
- Magnolia Medical Technologies, Inc.
- Reason for Recall:
- Product was shipped with the incorrect Transfer Adapter Instructions For Use (IFU).
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access of a specimen from Catheter Port to BD Vacutainer¿ Blood Collection or Urine Collection Tubes.
Product Codes/Lot Numbers:
Catalog #: 27BD-EN, Part #: P00165-000 Lot #9448037
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2393-2021
Related Recalls
Class I - Dangerous
Due to an uptick of complaints associated with premature needle retraction of blood collection system.