Sensis with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/o
Summary
The FDA issued a Class II for Sensis with software version VD12A. A diagnostic and administrative tool suppo by Siemens Medical Solutions USA, Inc. Reason: Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of its communication during the first patient examination of the day or afte.
Details
Source
Device Recall
External ID
Z-1425-2022
Action Date
2022-07-27
Status
Ongoing
Category
device
Product Description
Sensis with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology Model:10764561
Lot/Code Info: UDI-DI: 04056869010137 Serial Numbers: 61331, 60015
Quantity Affected: 2 units
Reason for Recall
Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of its communication during the first patient examination of the day or after a longer period of inactivity to the Sensis Vibe system resulting in no vital signs being available.
Distribution
US Nationwide Distribution AZ FL KY MI OH PR TX
Type: Voluntary: Firm initiated
Recall Initiated: 2022-06-15
Company
Malvern, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 176 device recalls issued in the same week, part of 413 device-related FDA actions this month.
Siemens Medical Solutions USA, Inc has 277 FDA actions in our database, including 173 recalls and 104 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Siemens Medical Solutions USA, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Siemens Medical Solutions USA, Inc have FDA actions?
Siemens Medical Solutions USA, Inc has 277 FDA actions in our database, including 173 recalls and 104 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1425-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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