STREAMLAB - REFRIGERATED STORAGE MODULE 9000
Check against the official notice below — it lists the full affected range.
Siemens Healthcare Diagnostics has recalled 186 StreamLAB Refrigerated Storage Module 9000 units that may have been shipped without a required warning label regarding potential interference with pacemaker functionality. The affected products were distributed across 37 US states and multiple foreign countries, including Australia, Canada, and several European nations.
The specific recalled units can be identified by Siemens Material Numbers 10482426, 10464532, or 10635930, or by the UDI 00630414949765. The source document does not specify a remedy or what action affected consumers should take.
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: 186 StreamLAB Automation Modules Lot/code info: Siemens Material Numbers: 10482426, 10464532, 10635930; UDI: 00630414949765
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.