Recall StatusTerminated
Date Initiated2019-10-28
Date Terminated2022-05-17
Product Quantity30142 US; OUS 113841
Reason for Recall
The frequency of calibration for the Genius Tympanic Thermometer as stated in the operating manual may not ensure that thermometers always remain within the stated accuracy range ( 0.2C for Genius 2 and 0.3C for Genius 3 thermometers). The measurement readings drift upwards over time, which means that the thermometers could exceed the upper stated accuracy tolerance of +0.2C for Genius 2 or +0.3C for Genius 3.
Firm Action
Cardinal Health issued Correction Notice and Acknowledgement Form via overnight on October 28, 2019 to the direct consignees. The Medical Device Correction Notice provides instructions to our direct consignees to notify any customers who they may have further distributed affected product as to the market action. Letter states reason for recall, health risk and action to take:
Customers are instructed that if they have access to a Genius Checker/Calibrator to calibrate all affected Genius thermometers. Following calibration, customers are to contact Cardinal Health Service & Repair to schedule and arrange for the software update on their Genius Checker/Calibrator. Once the updated Genius Checker/Calibrator has been returned to your facility, recalibrate all thermometers. If a customer does not have access to a Genius Checker/Calibrator, they are instructed to contact Cardinal Health Service & Repair to schedule and arrange for their thermometer(s) to be sent to a service center.
Contact Cardinal Health Service & Repair to schedule and arrange for your thermometer(s) to be sent to one of our service centers.
Monday Friday between 8:00am - 8:00pm EST
Service and Repair Line 877-227-3462, Option 1
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide Distribution - US Nationwide and Foreign in the countries of:
Australia
Austria
Belgium
Canada
Canary Islands
Chile
Costa Rica
Croatia
Cyprus
Czech Republic
Denmark
Egypt
Estonia
Finland
France
French Guiana
French Polynesia
Gabon
Germany
Gibraltar
Greece
Guadeloupe
Hong Kong
Iran, Islamic Republic Of
Ireland
Israel
Italy
Kuwait
Liechtenstein
Luxembourg
Martinique
Mayotte
Mexico
Netherlands
New Caledonia
New Zealand
Norway
Panama
Philippines
Poland
Portugal
Puerto Rico
Qatar
Reunion
Romania
San Marino
Saudi Arabia
Singapore
Slovakia
Slovenia
South Africa
South Korea
Spain
Swaziland
Sweden
Switzerland
Taiwan
Thailand
Turkey
United Arab Emirates
United Kingdom
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.