PlainRecalls
FDA Devices Moderate Class II Ongoing

Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"

Reported: March 27, 2024 Initiated: January 9, 2024 #Z-1313-2024

Product Description

Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"

Reason for Recall

Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In refrigerator due to mechanical failures, causing temperatures to fall below the validated range of 35.6 - 46.4 Degrees Fahrenheit (2 - 8 Degrees Celsius) for up to 60 minutes which could increase the probability of an incorrect test result or a delayed test result.

Details

Units Affected
25 units
Distribution
US Nationwide distribution in the states of AZ, PA and TX.
Location
Richmond, VA

Frequently Asked Questions

What product was recalled?
Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST". Recalled by Mckesson Medical-Surgical Inc. Corporate Office. Units affected: 25 units.
Why was this product recalled?
Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In refrigerator due to mechanical failures, causing temperatures to fall below the validated range of 35.6 - 46.4 Degrees Fahrenheit (2 - 8 Degrees Celsius) for up to 60 minutes which could increase the probability of an incorrect test result or a delayed test result.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 27, 2024. Severity: Moderate. Recall number: Z-1313-2024.