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Recall database

Waismed Ltd. recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–2 of 2 recalls

Class IIOngoingZ-2119-2025

Waismed Ltd. recalls Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 10…

Due to manufacturing error, Intraosseous device built-in stabilizer may not be released properly after deployment and insertion.

Waismed Ltd.Jul 23, 2025

Class IIOngoingZ-2118-2025

Waismed Ltd. recalls Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 1…

Due to manufacturing error, Intraosseous device built-in stabilizer may not be released properly after deployment and insertion.

Waismed Ltd.Jul 23, 2025