Waismed recalls

Waismed appears in 3 official U.S. recall notices indexed by RecallRadar, most recently on 2025-07-23.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000908 Software Version: N/A Product Description: NIO…
  FDA Device · Class II · 2025-07-23 · Waismed
• Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000603 Software Version: N/A Product Description: NI…
  FDA Device · Class II · 2025-07-23 · Waismed
• NIO-A / NIO-P is an instant IO access device comprises housing with spring load mechanism that injects a trocar needle into the bone marrow…
  FDA Device · Class II · 2016-09-07 · Waismed