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. 2,349 recalls have been distributed to South Dakota in the last 12 months.
Showing 26361–26380 of 47,632 recalls
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Two- Lumen Central Venous Catheterization Kit with Blue...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump 3010 Series The Medfusion¿ Syringe Infusion Pumps...
The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump 3500 Series The Medfusion¿ Syringe Infusion Pumps...
The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump 4000 Series The Medfusion¿ Syringe Infusion Pumps...
The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to Superpotent
The Issue: Superpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nexterone (amiodarone HCl) Premixed Injection Recalled by Baxter Healthcare...
The Issue: Presence of Particulate Matter:Particulate identified as polyethylene, the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iQ200 Series Urine Microscopy Analyzer with Barcode Reader Model NFT-2100...
The Issue: iQ200 Series Urine Microscopy Analyzer may intermittently fail to read urine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution - Premixed Dialysate for Hemodialysis with...
The Issue: Using different fluid formulations of NxStage PureFlow B Solution at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista System LOCI 8 CALIBRATOR The LOCI 8 Calibrator Recalled by...
The Issue: An increase in the number of failed calibration events or negative bias with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClariVein IC infusion catheter Recalled by Vascular Insights, LLC Due to...
The Issue: Certain catheters could have a compromised catheter shaft due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GERICARE Eyewash Recalled by Kareway Products Inc Due to Non-sterility:...
The Issue: Non-sterility: confirmed microbial contamination with Achromobacter xylosoxidans
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by Mayne Pharma Inc Due to Failed...
The Issue: Failed Dissolution Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clozapine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Tablet/Capsule Specifications; potential presence of broken tablets.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.