Product Recalls in South Dakota
Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,365 recalls have been distributed to South Dakota in the last 12 months.
Showing 24261–24280 of 27,558 recalls
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Intermittent noise on...
The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Essenta DR Recalled by Philips Medical Systems, Inc. Due to X-ray...
The Issue: X-ray system C-arm casting may loosen and fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Cyclosporine Flex reagent cartridge an in vitro diagnostic...
The Issue: Complaints were received regarding variability in recovery of QC and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5/C5 Heart-lung machine Product Usage: The StOckert S5/ Sorin C5 Recalled...
The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invivo Corporation Expression Information Portal (Model IP5) is intended to...
The Issue: Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Recalled by...
The Issue: The recalling firm determined that visual inspections of the fork joints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System (Brilliance CT Big Bore Oncology & Recalled...
The Issue: Machine Name in TumorLOC Basic Mode is obscured. When TumorLOC is in Basic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CP5 centrifugal pump system Product Usage: The Stockert S5/ Sorin Recalled...
The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach Irrigation Clip 40 Product Usage: Irrigation clips provide a...
The Issue: The Irrigation Clips were assembled with the incorrect (smaller) clips.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABACUS TPN Calculation Software Recalled by Baxter Corporation Englewood Due...
The Issue: Baxter Healthcare Corporation is issuing a voluntary correction for ABACUS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAS Omni Immune Controls Recalled by Microgenics Corporation Due to The...
The Issue: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAS Omni Immune PRO Controls Recalled by Microgenics Corporation Due to The...
The Issue: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: steroEOS Workstation with software versions: 1.3 Recalled by EOS Imaging Due...
The Issue: Error copying information to the clinical file and to the report when two 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carescape Patient Data Module The Patient Data Module Recalled...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular Screw 6.5mmx35mm Part Number: 010001000 Recalled by Biomet,...
The Issue: Investigation identified that the outer label, inner label, and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Secure II Med/Surg Bed Secure II and the 3002 S3 Recalled by Stryker Medical...
The Issue: Stryker Medical has identified a potential issue associated with Secure II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Camino Advanced Monitor with Waveform Display Model CAM01 Integra...
The Issue: Integra became aware through a complaint from a single non-US customer that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S3 Med/Surg Bed Secure II and the 3002 S3 are Recalled by Stryker Medical...
The Issue: Stryker Medical has identified a potential issue associated with Secure II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra LifeSciences is voluntarily recalling any unexpired lots of HITHSP10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.