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 19761–19780 of 47,632 recalls
Recalled Item: Rifampin for Injection Recalled by Mylan Laboratories Limited (Sterile...
The Issue: Failed Impurities/Degradation Specifications: discoloration due to elevated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Star 8 Rolling Walker/Rollator Recalled by Nova Ortho-Med Inc Due to Walkers...
The Issue: Walkers within the identified serial range have the potential for the front...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxymetry Cable Recalled by Edwards Lifesciences, LLC Due to Intermittent...
The Issue: Intermittent communication due to inconsistent crimping of connectors onto...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Legacy 3 Implant Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Some dental implant packages contain incorrect implants, which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer (DxH SMS) and UniCel DxH Slidemaker Recalled...
The Issue: When the UniCel DxH Slidemaker Stainer and UniCel DxH Slidemaker Stainer II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software versions syngo CT VB20 running on the following Siemens Recalled by...
The Issue: Software issue identified in the software versions syngo CT VB20 running on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAG SCREW 3.2MM GUIDE PIN SLEEVE Recalled by Smith & Nephew, Inc. Due to LAG...
The Issue: LAG SCREW 3.2 GUIDE PIN SLEEVE are being recalled due to a manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Oral Solution 5mg per 5mL Recalled by...
The Issue: Presence of Foreign Substance; Fiber particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Model Number: 06917259001 UDI: 04015630976010 - Product Usage: The System...
The Issue: The firm became aware of a cleaning solution leaking issue from the middle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 111" 10 Drop Admin Set w/2 Inj Sites Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Homocysteine-In vitro test for the quantitative determination of total...
The Issue: Homocysteine Reagent, Calibration Failures and Quality Control Recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.