Magnolia Medical Technologies, Inc.
Magnolia Medical Technologies, Inc. holds FDA 510(k) medical device clearances, cleared in 2020, with 2 FDA device recalls on record.
Top product codes for Magnolia Medical Technologies, Inc.
FDA recalls by Magnolia Medical Technologies, Inc.
- Z-0318-2022 — 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
- Z-2393-2021 — 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.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Magnolia Medical Technologies, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.