Siemens Medical Solutions USA, Inc Magnetom Allegra System. Nuclear Magnetic Resonance Imaging Diagnostic Device Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Magnetom Allegra System. Nuclear Magnetic Resonance Imaging Diagnostic Device
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
Model #7106433 - Serial #''s 20101 through 20113. Model #7387736 - Serial #''s 20405, 20406, 20411, 20412, and 20419
Products Sold
Model #7106433 - Serial #''s 20101 through 20113. Model #7387736 - Serial #''s 20405, 20406, 20411, 20412, and 20419
Siemens Medical Solutions USA, Inc is recalling Magnetom Allegra System. Nuclear Magnetic Resonance Imaging Diagnostic Device due to tissue roll can become magnetic. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
tissue roll can become magnetic
Recommended Action
Per FDA guidance
The recalling firm has issued Updated Instructions to replace the stainless steel tissue roll holder. The recalling firm''s representatives are visiting each account to replace the tissue roll holder.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, CT, FL, GA, IL, IN, KS, KY, MD, MA, MN, NY, NC, OH, OR, PA, TX, UT, DC
Page updated: Jan 10, 2026