Brand
Waismed Ltd.
2 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Waismed Ltd. and translate it into plain English — free weekly digest, optional same-day alerts.
- 2025-07-23FDA-DeviceClass IIBrand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000908 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intraosseous access device supplied Sterile and single use. Indicated for Intraosseous access to the Proximal humerus and Proximal Tibia in adult patients, in emergent situations. Component: N/A
Due to manufacturing error, Intraosseous device built-in stabilizer may not be released properly after deployment and insertion.
- 2025-07-23FDA-DeviceClass IIBrand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000603 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intra-osseous access device supplied Sterile and single use. Indicated for Intra-osseous access to the Proximal humerus and Proximal Tibia in adult patients, in emergent situations. Component: N/A
Due to manufacturing error, Intraosseous device built-in stabilizer may not be released properly after deployment and insertion.
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