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. 2,373 recalls have been distributed to South Dakota in the last 12 months.
Showing 22961–22980 of 27,558 recalls
Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has become aware of a potential safety issue involving missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...
The Issue: The software issue described was corrected in the modification to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Recalled by Teleflex Medical Due to Misbranding: Although the product...
The Issue: Misbranding: Although the product labeling identifies the catheters as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak Adaptor Recalled by Teleflex Medical Due to Possibility that the...
The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aqauapak 728 SW Recalled by Teleflex Medical Due to Possibility that the...
The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Uroskop Omnia Max system The Uroskop Omnia is a Recalled by Siemens...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens AXIOM Luminos dRF Max systems The Axiom Luminos dRF Recalled by...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Ysio Max system The Ysio Max is a radiographic system used in...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Luminos Agile Max system The Luminos Agile is intended Recalled by...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure IQ Evolve Mattress Recalled by Arjo Hospital Equipment AB Due to...
The Issue: The firm received complaints regarding multiple mattresses were showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dako Autostainer Link 48 with software version Dako Link 4.0.3 Recalled by...
The Issue: Dako is recalling the Dako Link 4.0.3 software on the Dako Autostainer Link...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eFilm Workstation 4.0 and 4.0.1. eFilm Workstation is one of Recalled by...
The Issue: There is an issue related to eFilm Workstation versions 4.0 and 4.0.1 when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Mass CKMB Isoenzyme Calibrator (MMB CAL) an in Recalled by...
The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista® Mass...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Charnley PN Retract & Handle Recalled by DePuy Orthopaedics, Inc. Due to The...
The Issue: The small extraction peg of the Charnley Pin Retractor and Handle set is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology" Hemo intended for complete physiological/hemodynamic...
The Issue: Software Error: The McKesson Cardiology Hemo calculation section incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Ysio Systems with software version VC10 The Ysio enables Recalled by...
The Issue: Siemens discovered that an unlikely error may occur on the Ysio system with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.