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Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc Recalls

All product recalls associated with Siemens Medical Solutions USA, Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 17761–17780 of 21320 recalls

Siemens Medical Solutions USA, Inc: AXIOM Artis System dTA using software version VB31D with ...

System may switch to emergency fluoroscopy mode.

FDAAug 25, 2008Nationwide• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: AXIOM Artis System dMP using software version VB31D with ...

System may switch to emergency fluoroscopy mode.

FDAAug 25, 2008Nationwide• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: AXIOM Artis System dTC using software version VB31D with ...

System may switch to emergency fluoroscopy mode.

FDAAug 25, 2008Nationwide• Siemens Medical Solutions USA, Inc

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Pointe Scientific, Inc.: Liquid AST (SGOT) Reagent Set, Manufactured by Pointe Sci...

The R1 component may be contaminated with Serratia liquefaciens, resulting decreased absorbances and failure of the reagent to produce test results.

FDAAug 25, 2008Nationwide• Pointe Scientific, Inc.

Medtronic Neuromodulation: Medtronic SynchroMed EL Programmable Pump, Model 8626-10....

Medtronic issued a letter to healthcare professionals providing important safety information regarding MRI (magnetic resonance imaging) effects on SynchroMed EL and SynchroMed II implantable infusion pumps. As stated in product labeling, the magnetic field of an MRI will temporarily stop the rotor of the pump motor and suspend drug infusion for the duration of MRI exposure for all SynchroMed pump

FDAAug 25, 2008WA, PR• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic SynchroMed II Programmable Pump, Model 8637-20....

FDAAug 25, 2008WA, PR• Medtronic Neuromodulation

Boston Scientific Corporation: Platinum Plus" LT , REF 46-602, UPN M001466020, LT/0.018...

Boston Scientific is initiating a voluntary recall of the Platinum Plus" Guidewire (peripheral). BSC has received reports that product may be labeled as a 260 CM long guidewire when the actual packaged device is a 180 CM long guidewire and the product may be labeled as a 180 CM long guidewire when the actual packaged device is a 260 CM long guidewire. There is no expected potential for injury to

FDAAug 25, 2008CA, FL, GA +16 more• Boston Scientific Corporation

Pointe Scientific, Inc.: AST R1 Reagent, 120 ml., Pointe Scientific, Inc., Canton,...

The R1 component may be contaminated with Serratia liquefaciens, resulting decreased absorbances and failure of the reagent to produce test results.

FDAAug 25, 2008Nationwide• Pointe Scientific, Inc.

Siemens Medical Solutions USA, Inc: AXIOM Artis System dBA using software version VB31D with ...

System may switch to emergency fluoroscopy mode.

FDAAug 25, 2008Nationwide• Siemens Medical Solutions USA, Inc

Telefelx Medical: Weck Hemoclip Plus Ligating Clips, Rx Only, Sterile, Tele...

A hole in the sterile unit blister pack was detected that would compromise sterility.

FDAAug 22, 2008Nationwide• Telefelx Medical

Telefelx Medical: Weck Hemoclip Traditional Ligating Clips, Rx Only, Steril...

A hole in the sterile unit blister pack was detected that would compromise sterility.

FDAAug 22, 2008Nationwide• Telefelx Medical

Telefelx Medical: Weck , Horizon Titanium Clips, Rx Only, Sterile, Teleflex...

A hole in the sterile unit blister pack was detected that would compromise sterility.

FDAAug 22, 2008Nationwide• Telefelx Medical

Siemens Medical Solutions USA, Inc: Axiom Artis Zee. Angiographic X-ray System.

Patients could possibly fall off the table if not properly secured when: 1) moving them onto the patient table, 2) moving them on the patient table or 3) removing them from the patient table.

FDAAug 22, 2008Nationwide• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: Syngo Imaging with versions VB20B, VB20D, VB20F, VB20G, V...

Image may not be visible after merge.

FDAAug 22, 2008Nationwide• Siemens Medical Solutions USA, Inc

Telefelx Medical: WECK HemoClip Auto, Rx Only, Sterile, Teleflex Medical, R...

A hole in the sterile unit blister pack was detected that would compromise sterility.

FDAAug 22, 2008Nationwide• Telefelx Medical

Draeger Medical, Inc.: Draeger Medical Apollo Anesthesia Machine, catalog number...

Sporadic errors in various device functions, including low readings of the single gas flows for oxygen, nitrous oxide, or air delivery, or mechanical ventilation failure. Alarms and error messages function as designed.

FDAAug 22, 2008Nationwide• Draeger Medical, Inc.

Telefelx Medical: WECK Hem-o-lok Non-absorbable Polymer Ligation Clips, Rx ...

A hole in the sterile unit blister pack was detected that would compromise sterility.

FDAAug 22, 2008Nationwide• Telefelx Medical

Siemens Medical Solutions USA, Inc: AXIOM Artis. Angiographic X-ray System.

Patients could possibly fall off the table if not properly secured when: 1) moving them onto the patient table, 2) moving them on the patient table or 3) removing them from the patient table.

FDAAug 22, 2008Nationwide• Siemens Medical Solutions USA, Inc

Philips Medical Systems North America Co. Phillips: Allura Xper FD10 Monoplane X-ray system. Intended for use...

Due to a potential geometry software lock up during a Digital Rotational Angiography (DRA) run, the stand and table movement may no longer be possible.

FDAAug 21, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Allura Xper FD10/10 Biplane X-ray system. Intended for us...

Potential for table and stand not to move due to a software error.

FDAAug 21, 2008Nationwide• Philips Medical Systems North America Co. Phillips