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. 970 recalls have been distributed to South Dakota in the last 12 months.
Showing 27441–27460 of 47,632 recalls
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Cardioplegia Adapter with Pressure Port Provides access for a Recalled...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GC80 Digital X-ray Imaging System Recalled by NeuroLogica Corporation...
The Issue: An image was obtained with over exposure during a Thorax examination using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Antegrade/Retrograde Adapter Method for perfusion of cardioplegia...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION Recalled by Quidel Corporation Due...
The Issue: In-house testing revealed the presence of plastic spurs at the tips of some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Extension Line Adapters 20 in length Used to extend Recalled by...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pressure Disposable Pressure Display Sets Extends the pressure line...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pressure Monitoring Extension Line Adapters Extends the pressure line...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paroxetine Extended-Release Tablets USP Recalled by Lupin Pharmaceuticals...
The Issue: Failed Dissolution Specifications: out of specification observed in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.