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. 2,484 recalls have been distributed to South Dakota in the last 12 months.
Showing 13261–13280 of 47,632 recalls
Recalled Item: MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors -...
The Issue: The External Retention Bolster contained in the kit may be a larger diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Chuck-The Universal Chuck is an Instrument Handle provided as...
The Issue: Top cap may loosen and detach if the Universal Chuck becomes jammed and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC* Percutaneous Endoscopic Gastrostomy PEG Kit - 20 Fr-PULL Recalled by...
The Issue: The External Retention Bolster contained in the kit may be a larger diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmunoPass Recalled by Empowered Diagnostics LLC Due to COVID test kits were...
The Issue: COVID test kits were offered for sale and distributed to consumers in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CovClear COVID-19 Rapid Antigen Test Recalled by Empowered Diagnostics LLC...
The Issue: COVID test kits were offered for sale and distributed to consumers in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medroxyprogesterone Acetate Injection Recalled by Ideal Specialty...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups Recalled by Lohxa, LLC...
The Issue: Microbial Contamination of Non-Sterile Product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefixime Capsules Recalled by Ascend Laboratories, LLC Due to Failed...
The Issue: Failed impurities/degradation specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Endurant Recalled by Medtronic Vascular, Inc. Due to Stent Graft Systems...
The Issue: Stent Graft Systems built with specific batches of taper tip assemblies have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by American Health...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Inositol packaged in white plastic bottle with and Recalled by Professional...
The Issue: Product recalled due to undeclared niacin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vitamin B Complex packaged in white plastic bottle labeled in part Recalled...
The Issue: Product recalled due to undeclared niacin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 100% Plant-Based Dream Pops Vanilla Sky Bites Recalled by DREAM POPS Due to...
The Issue: Undeclared allergen; milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 100% Plant-Based Dream Pops Berry Dreams Bites Recalled by DREAM POPS Due to...
The Issue: Undeclared allergen; milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 100% Plant-Based Dream Pops Birthday Cake Bites Recalled by DREAM POPS Due...
The Issue: Undeclared allergen; milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 100% Plant-Based Dream Pops Cookie Dough Bites Recalled by DREAM POPS Due to...
The Issue: Undeclared allergen; milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: bellavista 1000 ventilator Recalled by Vyaire Medical Due to Potential...
The Issue: Potential cessation in ventilation can occur under specific conditions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flat Panel Detector Recalled by Canon Medical System, USA, INC. Due to...
The Issue: Abnormal images such as horizontal stripes may be displayed and recovery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NobelReplace Conical Connection RP 4.3x11.5 mm STERILE R Recalled by Nobel...
The Issue: Due to 16 complaints related to drivers not engaging in implants. According...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chameleon PTA Balloon Dilation Catheter 8 mm x 40 mm Recalled by Covidien...
The Issue: The firm has received six (6) complaint reports from customers indicating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.