Magnolia Medical Technologies, Inc. FDA Recalls

2 recalls on file across devices, 0 of them Class I and 0 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection SysClass IINov 2, 2021Due to an uptick of complaints associated with premature nee	Due to an uptick of complaints associated with premature needle retraction of blood collection system.	Class IIDevices	Nov 2, 2021
Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access oClass IIAug 2, 2021Product was shipped with the incorrect Transfer Adapter Inst	Product was shipped with the incorrect Transfer Adapter Instructions For Use (IFU).	Class IIDevices	Aug 2, 2021