TEMPUS IC PROFESSIONAL Patient Monitor, Part No. 00-1002, Manufactured by: Remote Diagnostics Technologies Ltd., The Old
FDA device recall Z-2183-2011 · posted 2011-05-11 · Terminated
Recall details
- Recalling firm
- Remote Diagnostic Technologies Ltd.
- Reason for recall
- It was discovered that when a 12 Lead ECG is recorded and monitoring is quickly restarted, the ECG can cease functioning.
- Action taken
- Remote Diagnostic Technologies, Ltd notified its consignees of the problem and the work-around via letter with the subject line "ECG Issue - Field Action Required" on 03/25/2011. The letter stated that customers can avoid the issues by viewing the recorded ECG for at least 13 seconds. Two diagrams were attached with the letter depicting the conditions under which the issue can occur. Customers can continue to use the device normally in all other respects. The letter states that the firm is working on a software modification which will permanently fix the issue and prevent it from occurring. Customers are to contact the Regulatory Affairs and Operations Manager if they have any questions.
- Root cause
- Component change control
- Status
- Terminated
- Product code
- MWI
- Quantity affected
- 19 units
- Distribution
- Nationwide Distribution -- KY, MD, VA, and FL.
- Date initiated
- 2011-03-25
- Date posted
- 2011-05-11
- Date terminated
- 2011-09-16
- Location
- Basingstoke Hampshire, United Kingdom
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| TEMPUS IC PROFESSIONAL PATIENT MONITOR (K101264) | Remote Diagnostic Technologies , Ltd. | 2010-05-11 |