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.
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. Distribution: US Nationwide distribution in the states of MO, MN, MA, OH, NE. Quantity: 1 unit Lot/code info: UDI-DI: 00191072184566; Lot: 2405102; Exp: 05/10/2024
00191072184566
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.