Axiom Artis, Model Numbers: 5904433, 5904441, 5904649, 5904656, 5917054, 7007755, 7008605, 7412807, 7413078, 7555357, 7555373, 7727717, 7728350 & 7728392
Reported: March 7, 2018 Initiated: June 6, 2017 #Z-0708-2018
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
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- N/A
- Distribution
- U.S. Nationwide
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
Axiom Artis, Model Numbers: 5904433, 5904441, 5904649, 5904656, 5917054, 7007755, 7008605, 7412807, 7413078, 7555357, 7555373, 7727717, 7728350 & 7728392. Recalled by Siemens Medical Solutions USA, Inc. Units affected: N/A.
Why was this product recalled? ▼
Potential for liquid entry
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 7, 2018. Severity: Moderate. Recall number: Z-0708-2018.
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