Siemens Healthcare Diagnostics, Inc External power supply adaptors that accompany Clinitek Status Connect System The Clinitek Status system is a urine analyzer. Recall
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
External power supply adaptors that accompany Clinitek Status Connect System The Clinitek Status system is a urine analyzer.
Brand
Siemens Healthcare Diagnostics, Inc
Lot Codes / Batch Numbers
10703923, 10704041, 10376322, 10376323, 10470849, (Legacy P/N: 1797, 1790) Power supply adaptors embossed with the following numerical date codes: 50130, 51130, 52130, 01140, 02140, 03140, 04140, 05140, 06140, 07140, 08140, 09140, 10140, 11140, 12140, 13140, 14140, 15140, 16140, 17140, 18140, 19140, 20140, 21140, 22140, 23140
Products Sold
10703923, 10704041, 10376322, 10376323, 10470849; (Legacy P/N: 1797, 1790) Power supply adaptors embossed with the following numerical date codes: 50130, 51130, 52130, 01140, 02140, 03140, 04140, 05140, 06140, 07140, 08140, 09140, 10140, 11140, 12140, 13140, 14140, 15140, 16140, 17140, 18140, 19140, 20140, 21140, 22140, 23140
Siemens Healthcare Diagnostics, Inc is recalling External power supply adaptors that accompany Clinitek Status Connect System The Clinitek Status due to The external power supply for the Clintek Status analyzer, which is provided separately, is damaged. It can result in an electric shock to the User.. This is a Class I recall, indicating a high risk of serious health consequences or death. Based on FDA medical device enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The external power supply for the Clintek Status analyzer, which is provided separately, is damaged. It can result in an electric shock to the User.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026