FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: Magnetom Allegra System. Nuclear Magnetic Resonance Imaging Diagnostic Device
- Recall number
- Z-0522-04
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- Magnetom Allegra System. Nuclear Magnetic Resonance Imaging Diagnostic Device
- Status
- Terminated
- Initiated
- 2003-12-18
- Posted
- 2004-02-10
- Terminated
- 2004-11-09
- Reason
- tissue roll can become magnetic
- Root cause
- Other
- Action
- 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.
- Quantity
- 16 units
- Distribution
- The product was shipped to medical facilities in CA, CT, DC, FL, GA, IL, IN, KS, KY, MA, MD, MN, NC, NY, OH, OR, PA, TX, and UT.
- Lot, serial or model codes
- Model #7106433 - Serial #''s 20101 through 20113. Model #7387736 - Serial #''s 20405, 20406, 20411, 20412, and 20419
- 510(k) numbers
- ["K002179"]
- PMA numbers
- not on file
- Product code
- not on file
- Firm FEI
- 2240869
- Firm city
- Malvern
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28