PlainRecalls
FDA Devices Moderate Class II Ongoing

Cysto, FTCY03L; Medical convenience kit

Reported: October 2, 2024 Initiated: August 7, 2024 #Z-3243-2024

Product Description

Cysto, FTCY03L; Medical convenience kit

Reason for Recall

ACS identified that due to an inoperable chart recorder, humidity readings were out-of-specification in one of the controlled environment areas. As a result, ACS is unable to confirm product sterilization assurance requirements were met.

Details

Units Affected
36 units
Distribution
US Nationwide distribution in the states of MO, MN, MA, OH, NE.
Location
Kansas City, MO

Frequently Asked Questions

What product was recalled?
Cysto, FTCY03L; Medical convenience kit. Recalled by American Contract Systems, Inc.. Units affected: 36 units.
Why was this product recalled?
ACS identified that due to an inoperable chart recorder, humidity readings were out-of-specification in one of the controlled environment areas. As a result, ACS is unable to confirm product sterilization assurance requirements were met.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 2, 2024. Severity: Moderate. Recall number: Z-3243-2024.