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. 2,386 recalls have been distributed to South Dakota in the last 12 months.
Showing 20681–20700 of 47,632 recalls
Recalled Item: SPECTRALIS with HEYEX2 image management system. a non-contact ophthalmic...
The Issue: Error in the default configuration which could lead to the incorrect display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LivaNova SMART PERFUSION PACK INSPIRE 8S - Product Usage: The Recalled by...
The Issue: Perfusion tubing pack was packaged with the incorrect cuvette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEMO No Needle Corrugated Carton 20 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEMO No Needle Corrugated Carton 40 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Drive Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Edge Plus Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric...
The Issue: The firm conducted internal investigations that confirmed customer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAsymphony SP SOW 5.0.3 Recalled by Qiagen Sciences LLC Due to QIAsymphony...
The Issue: QIAsymphony software version 5.0.3 - Software issue incorreclty assigns the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blanketrol II Hyper-Hypothermia System Recalled by Cincinnati Sub-Zero...
The Issue: Warnings statements have been added- exceeding 40 degree C for extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blanketrol III Hyper-Hypothermia System- body hypothermia system temperature...
The Issue: Warnings statements have been added- exceeding 40 degree C for extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoolBlue Hyper-Hypothermia System- body hypothermia system Model: Innercool...
The Issue: Warnings statements have been added- exceeding 40 degree C for extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altaire Homatropaire Homatropine Hyrdobromide Opthalmic Solution Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kaitlib Fe norethindrone and ethinyl estradiol chewable tablets (0.8...
The Issue: Failed Impurities/Degradation Specifications: Kaitlib Fe Tablets has an out...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.