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 29521–29540 of 47,632 recalls
Recalled Item: Midazolam HCl all strengths Recalled by Advanced Pharma Inc. Due to...
The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropivacaine HCl in 0.9% Sodium Chloride all strengths Recalled by Advanced...
The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Succinylcholine Chloride all strengths Recalled by Advanced Pharma Inc. Due...
The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epinephrine HCl all strengths Recalled by Advanced Pharma Inc. Due to...
The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropi/ Epi/ Clon PeriCapsular injection all strengths Recalled by Advanced...
The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: INFINITY Internal Hex Healing Abutment Recalled by Ace Surgical Supply Co.,...
The Issue: Incorrect device was packaged.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Two-Bite Turtle Brownie Party Platter 16 x 12.2 oz (346g) item number 09904...
The Issue: Dried weevil larvae may be present in the recalled products.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bobo's Coconut Oat Bar 3oz. Packaged in overwrap film per single bar...
The Issue: Bobo's recalled Coconut 3oz Bar due to mold.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Two-Bite Pecan Tarts Party Platter 16 x 16.2 (460g) item number 09877...
The Issue: Dried weevil larvae may be present in the recalled products.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Two-Bite Pecan Tart 9.2 oz (261g) item number 02023 Recalled by Give and Go...
The Issue: Dried weevil larvae may be present in the recalled products.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Bakery Mini Pecan Tarts Part Platter NET WT 16x Recalled by Give and Go...
The Issue: Dried weevil larvae may be present in the recalled products.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: La Fe Papa Criollas Yellow Potato Net Wt. 14 oz. Recalled by Grace Kennedy...
The Issue: La Fe Papas Criollos may be contaminated with Listeria Monoctyogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Pads Recalled by Terumo...
The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartTools Knee System Orthopedic Stereotaxic Instrument Recalled by...
The Issue: There has been an increase in the number of complaints regarding bent or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 16 TruePoint TrueV - 4R Recalled by Siemens Medical Solutions USA...
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Gel Pads Product Recalled...
The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 16 TruePoint - 3R Recalled by Siemens Medical Solutions USA Inc....
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS-636 Recalled by Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc....
The Issue: Incorrect priming volume printed on the device package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.