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. 1,660 recalls have been distributed to South Dakota in the last 12 months.
Showing 46341–46360 of 47,632 recalls
Recalled Item: Wildwood Emerald Valley Kitchen Organic Mild Salsa Recalled by Pulmuone...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Organic Medium Salsa Recalled by Pulmuone Wildwood Inc Due to The...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Organic Mild Salsa Recalled by Pulmuone Wildwood Inc Due to The...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Medium Salsa Recalled by Pulmuone...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Mild Salsa - Canada (containing...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Medium Salsa - Canada (containing...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Hot Salsa Recalled by Pulmuone...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alere Triage TOX Drug Screen 9 Panel Recalled by Alere San Diego, Inc. Due...
The Issue: Alere San Diego is recalling Alere Triage TOX Drug Screen because there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD Recalled...
The Issue: The 4 degree and 9 degree trial instruments (SJ768T-US/SJ780T-US) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System Recalled by Actavis Due to Subpotent; some...
The Issue: Subpotent; some patches may not contain fentanyl gel
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ventlab Rescue Med Infant Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Narrow CrossFit (NC) Screw for CARES Abutment ZrO2. Endosseous...
The Issue: Incorrect Screw (RC) included with NC CARES Abutment Set was not a Narrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MultiDiagnost Eleva with Flat Detector (MD Eleva FD)Model: 708034...
The Issue: When doing a 3 Dimensional Rotational Angiography (3DRA) the 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breath Tech Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Premium Small Child Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stat-Check Resuscitator Recalled by Ventlab Corporation Due to Possible...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.