Every recall we track for Waismed Ltd. — 2 in all — plus the complaints and injury reports the public filed about them.
Waismed Ltd. recalls NIO Intraosseous Device Adult Model 105000603 due to manufacturing error causing stabilizer to not release properly after deployment. Affected units have lot numbers 2440043, 2440045, 2540046, 2540047.
Waismed Ltd. recalls NIO+ Intraosseous Device Adult Model 105000908 due to potential stabilizer malfunction after deployment. This device is for emergency use in adult patients. Affected units have specific lot codes and were sold with a UDI.
