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. 2,558 recalls have been distributed to South Dakota in the last 12 months.
Showing 401–420 of 47,632 recalls
Recalled Item: *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm...
The Issue: Increased reports of stent deployment and expansion issues. The most common...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 8mm x 8mm Recalled...
The Issue: Increased reports of stent deployment and expansion issues. The most common...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification...
The Issue: To remove the software applications from certain CT systems as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alphenix INFX-8000F Recalled by Canon Medical System, USA, INC. Due to It...
The Issue: It has been discovered that there is a possibility that the fixing screws of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alphenix INFX-8000H Recalled by Canon Medical System, USA, INC. Due to It...
The Issue: It has been discovered that there is a possibility that the fixing screws of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alphenix INFX-8000V Recalled by Canon Medical System, USA, INC. Due to It...
The Issue: It has been discovered that there is a possibility that the fixing screws of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alphenix INFX-8000C Recalled by Canon Medical System, USA, INC. Due to It...
The Issue: It has been discovered that there is a possibility that the fixing screws of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tego Connector: Recalled by ICU Medical, Inc. Due to Needle free access...
The Issue: Needle free access device intended as accessory to vascular access used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column...
The Issue: The supplier manufactured anatomical left plates with an incorrect thread...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column...
The Issue: The supplier manufactured anatomical left plates with an incorrect thread...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VANTAGE GALAN 3T Model MRT-3020/MEXL-3020 Recalled by Canon Medical System,...
The Issue: There is a potential for formation of ice occurring in the venting system of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulsator Arterial Blood Sampling Kit Recalled by ICU Medical Inc. Due to...
The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VANTAGE TITAN 3T Model MRT-3010/MEXL-3010 Recalled by Canon Medical System,...
The Issue: There is a potential for formation of ice occurring in the venting system of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Spinal Tray Recalled by ICU Medical Inc. Due to Affected lots of...
The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL Recalled by Imprimis NJOF, LLC Due to...
The Issue: Presence of particulate matter - Glass like particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone Moxifloxacin Ketorolac Recalled by Imprimis NJOF, LLC Due to...
The Issue: Presence of particulate matter - Glass like particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone Moxifloxacin Recalled by Imprimis NJOF, LLC Due to Presence of...
The Issue: Presence of particulate matter - Glass like particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gelsoft Plus Recalled by Vascutek, Ltd. Due to Gelatin sealed woven...
The Issue: Gelatin sealed woven polyester prostheses devices, designed for vascular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...
The Issue: Potential for fraying on the body support strap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...
The Issue: Potential for fraying on the body support strap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.