FDA Device recall Z-1313-2024
Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"
- FDA Device
- Class II
- ongoing
- Published 2024-03-27
On 2024-03-27 the FDA classified a Class II recall of Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST" by Mckesson Medical Surgical Corporate Office, citing 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 D….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1313-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-01-09 |
| Published | 2024-03-27 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Mckesson Medical Surgical Corporate Office |
| Distribution | US |
Product
Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"
Reason
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.
Identifiers
| code_info | Catalogue Number: LCC101; UDI/DI: 10724995220072 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1313-2024%22
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