Waismed Ltd. Recalls
2 recalls from federal safety databases (FDA, CPSC). Sourced directly from government enforcement feeds.
Medical Device Recalls (2)
- Class II
June 5, 2025
Brand 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 acces
Due to manufacturing error, Intraosseous device built-in stabilizer may not be released properly after deployment and insertion.
- Class II
June 5, 2025
Brand 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 acc
Due to manufacturing error, Intraosseous device built-in stabilizer may not be released properly after deployment and insertion.
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