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. 2,491 recalls have been distributed to South Dakota in the last 12 months.
Showing 11001–11020 of 27,558 recalls
Recalled Item: Siemens epoc BGEM Test Card-In vitro diagnostic device for the Recalled by...
The Issue: Sporadically inconsistent discrepant (low bias) glucose results on card lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Albumin Gen.2 Recalled by Roche Diagnostics Operations, Inc. Due to Roche...
The Issue: Roche has confirmed customer complaints of low quality (QC) recovery and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tina-quant Complement C4 ver.2 Recalled by Roche Diagnostics Operations,...
The Issue: Roche has confirmed customer complaints of low quality (QC) recovery and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Xtreme (PTCA Balloon Dilation Catheter) Recalled by ev3 Inc. Due to...
The Issue: Labeling discrepancy for the Rated Burst Pressure (RBP) value.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BECKMAN COULTER ACCESS Immunoassay Systems - Access Unconjugated Estriol...
The Issue: Due to alkaline phosphatase (ALP) associated interference causing falsely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...
The Issue: Subsequent failure of catheters in the field and failed quality testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...
The Issue: Subsequent failure of catheters in the field and failed quality testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista Akaline Phosphatase (ALPI) Flex reagent cartridge -...
The Issue: Low outlier resultsgenerated with Alkaline Phosphatase (ALPI) Flex reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...
The Issue: Subsequent failure of catheters in the field and failed quality testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM HER-2/neu (H2n) assay Recalled by Siemens Healthcare...
The Issue: Siemens confirmed that the Upper Limit of Normal (ULN) as claimed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquas PowerFlow Tube Set - Product Usage: The device delivers Recalled by...
The Issue: The product design incorporating a motor driven impeller pump powered by one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x1/16 UAS BLK...
The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x3/32 Recalled...
The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 3/8x3/32 Recalled...
The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Opticross 35 15 MHz Peripheral Imaging Catheter 8F (2.74 mm) Recalled by...
The Issue: Opticross 35 Peripheral Imaging Catheter is being recalled because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health"...
The Issue: The third-party brand latex micro surgical gloves packaged within specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inquiry Steerable Diagnostic Catheter Recalled by Irvine Biomedical Inc, a...
The Issue: Steerable diagnostic catheter packages labeled Model IBI-81104, batch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inquiry Steerable Diagnostic Catheter Recalled by Irvine Biomedical Inc, a...
The Issue: Steerable diagnostic catheter packages labeled Model IBI-81104, batch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imactis Patient Fiducial (Patient ) Recalled by Imactis Due to The firm has...
The Issue: The firm has received reports concerning the patient fiducial disk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SwiftHook sold as the following: a. Individually as SwiftHook b. Recalled by...
The Issue: Carry bar may detach during use of mobile lifts and ceiling lifts equipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.