Z-0772-2018 Class II Terminated
FDA device recall Z-0772-2018 was initiated by Steris Corporation on September 28, 2017 and is designated Class II. Reason for recall: Correction to update sterilizer software to prohibit the use of expired sterilant prior to the start of a sterilization cycle. The recall status is terminated (terminated September 12, 2018). Affected quantity: 406.
Recall Details
- Product Type
- Devices
- Report Date
- March 7, 2018
- Initiation Date
- September 28, 2017
- Termination Date
- September 12, 2018
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 406
Product Description
Reason for Recall
Distribution Pattern
Distributed in 44 states: AL, AK, AZ, AR, CA, CO, DE, FL, GA, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, WY; Puerto Rico, and the following countries: Algeria, Australia, Azerbaijan, Bahrain, Brazil, Brunei Darussalam, Bulgaria, Canada, Chile, Colombia, Costa Rica, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Hong Kong, Hungary, India, Israel, Italy, Republic of Korea, Kuwait, Latvia, Malaysia, Mexico, Morocco, Myanmar, Panama, Peru, Philippines, Poland, Portugal, Qatar, Saudi Arabia, South Africa, Spain, Switzerland, Thailand, Turkey, United Arab Emirates, and Vietnam.