Siemens Healthcare Diagnostics, Inc. recalls APTIO RACK OUTPUT MODULE
Recalled Product
APTIO RACK OUTPUT MODULE
Hazard / Issue
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
Issued by
FDA
Affected States: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, PA, SC, TN, TX, VA, WA, WV
Lot/Code Info: Siemens Material Numbers: 10715432, 10715434; UDI: 00630414594477
View official government recall
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