APTIO CENTRIFUGE MODULE
Check against the official notice below — it lists the full affected range.
Siemens Healthcare Diagnostics, Inc. has recalled 441 Aptio Centrifuge Modules due to the potential that units were shipped without a warning label for possible interference to pacemaker functionality. The affected modules were distributed across 38 U.S. states and multiple foreign countries including Australia, Canada, France, Germany, Italy, and others. The recalled products are identified by Siemens Material Numbers 10703032 and 10713761, with UDI 00630414594477.
The source record does not specify a remedy or what action affected consumers should take regarding this recall.
Written by software from the official notice below. Not reviewed by a lawyer.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
Reason for recall: The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality. Distribution: The products were distributed to the following US 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, and WV. The products were distributed to the following foreign countries: Australia, Austria, Bangladesh, Belgium, Canada, Croatia, France, Germany, Greece, Hong Kong, India, Indonesia, Italy, L Quantity: 441 Aptio Automation Modules Lot/code info: Siemens Material Numbers: 10703032, 10713761; UDI: 00630414594477
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.