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. 2,465 recalls have been distributed to South Dakota in the last 12 months.
Showing 14581–14600 of 27,558 recalls
Recalled Item: The Spirit Plus Bed Recalled by Stryker Medical Division of Stryker...
The Issue: The beds with the high rail side rail option may not be complaint with IEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemoglobin A1c Control Recalled by Tosoh Bioscience Inc Due to Tosoh...
The Issue: Tosoh Bioscience has become aware of potential degradation of HbA1c control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900 Automated Immunoassay Analyzer Recalled by Tosoh Bioscience Inc Due...
The Issue: Tosoh Bioscience has become aware of a potential issue with the axis base of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HEALTHCARE CARESCAPE R860 Inspiratory Safety Guard Recalled by GE...
The Issue: The ventilator Inspiratory Safety Guard (ISG) may disconnect from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...
The Issue: Tosoh Bioscience has become aware of a potential issue with the pickup arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parietex Composite Parastomal Mesh (Product Number PCOPM15 / PCOPM20)...
The Issue: The firm is issuing this voluntary removal following receipt of reports of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Omnibed - Product Usage: The OmniBed is a combination Recalled by...
The Issue: GE Healthcare has become aware of a potential safety issue that can occur if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 630G 6025805-003_C Recalled by Medtronic Inc. Due to...
The Issue: Reports of occurrences in which insulin pumps with version 4.10 software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect system Product Usage: The Signa Architect system is Recalled...
The Issue: A small area on the bore surface, which is normally accessible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF 550 x 5ML/H 6" CATH Recalled by Arrow International Inc Due to Possible...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF 550 x 5ML/H 6" DUAL CATHS Recalled by Arrow International Inc Due to...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF w/AS 550 x 1-14ML/HR 2ML-30LO CPNB Recalled by Arrow International Inc...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF w/AS 550x 0.5 7 ml/hr Recalled by Arrow International Inc Due to Possible...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF w/AS 550 x 1-14ML/HR 2ML-15LO CPNB Recalled by Arrow International Inc...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF w/AS 550 x 1-14ML/HR 5ML-60LO CPNB Recalled by Arrow International Inc...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermacare Muscle Pain Therapy HeatWraps: a) b) Recalled by Pfizer Inc. Due...
The Issue: The firm received complaints of the wrap coming apart and leaking granular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF550x5ML/H 2ML 60LO 6" DUAL CATHS Recalled by Arrow International Inc Due...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF 550 x 5ML/H FH DL 30hole SAT C Recalled by Arrow International Inc Due to...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF 550 x 5ML/HR CPNB Recalled by Arrow International Inc Due to Possible...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF 550 x 5ML/HR 2ML 60LO CPNB Recalled by Arrow International Inc Due to...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.