Z-0708-2018 Class II Terminated
FDA device recall Z-0708-2018 was initiated by Siemens Medical Solutions USA, Inc on June 6, 2017 and is designated Class II. Reason for recall: Potential for liquid entry The recall status is terminated (terminated May 16, 2019). Affected quantity: N/A.
Recall Details
- Product Type
- Devices
- Report Date
- March 7, 2018
- Initiation Date
- June 6, 2017
- Termination Date
- May 16, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- N/A
Product Description
Axiom Artis, Model Numbers: 5904433, 5904441, 5904649, 5904656, 5917054, 7007755, 7008605, 7412807, 7413078, 7555357, 7555373, 7727717, 7728350 & 7728392
Reason for Recall
Potential for liquid entry
Distribution Pattern
U.S. Nationwide
Code Information
10094135, 10094137, 10094141, 10094142, 10094143, 10280959, 10848280, 10848281, 10848282, 10848353, 10848354, 10848355, 5904433, 5904441, 5904649, 5904656, 5917054, 7007755, 7008605, 7412807, 7413078, 7555357, 7555373, 7727717, 7728350, 7728392