Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Recalled by Magnolia Medical Technologies, Inc. Due to Due to an uptick of complaints associated with...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Magnolia Medical Technologies, Inc. directly.
Affected Products
The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection System - 21G, Wide Neck 2700-23-EN / Steripath Gen2 Blood Collection System - 23G, Wide Neck 27BD-21-EN / Steripath Gen2 Blood Collection System - 21G, Long Neck 27BD-23-EN / Steripath Gen2 Blood Collection System - 23G, Long Neck
Quantity: 137,200 devices
Why Was This Recalled?
Due to an uptick of complaints associated with premature needle retraction of blood collection system.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Magnolia Medical Technologies, Inc.
Magnolia Medical Technologies, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report