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.

47,632 total recalls
1,660 in last 12 months

Showing 4588145900 of 47,632 recalls

Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 6.5 w/Needles with Orthocord Product Number: 222970 SPIRALOK...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 5.0mm with Panacryl and needles Product Number: 222961 SPIRALOK...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 6.5 w/out Needles with Orthocord Product Number: 222971 SPIRALOK...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· Philips Healthcare Inc.

Recalled Item: Philips Digital Diagnost-Mobile Detector Holder for Digital Diagnost (Single...

The Issue: The Wireless Portable Detector (WPD) is not fixed securely inside the Mobile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 6.5 w/out Needles with violet and blue Orthocord Product Recalled...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 6, 2012· Church & Dwight Inc

Recalled Item: Orajel Kids My Way! Anticavity Fluoride (sodium fluoride) toothpaste...

The Issue: CGMP Deviations: Product was made with an incorrect ingredient, Laureth-9...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 6, 2012· Eco Health, Inc.

Recalled Item: florAlign Prebiotic Formula Recalled by Eco Health, Inc. Due to Potential...

The Issue: Eco Health is recalling florAlign Prebiotic Formula because it has the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 6, 2012· Gills Onions, LLC

Recalled Item: 1/4" Slivered Yellow Onions Recalled by Gills Onions, LLC Due to Potential...

The Issue: Gills Onions is recalling diced and slivered onions because it may be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 6, 2012· Gills Onions, LLC

Recalled Item: 1/2" Diced Yellow Onions Recalled by Gills Onions, LLC Due to Potential...

The Issue: Gills Onions is recalling diced and slivered onions because it may be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 6, 2012· Gills Onions, LLC

Recalled Item: 1/4" Diced Red Onions Recalled by Gills Onions, LLC Due to Potential...

The Issue: Gills Onions is recalling diced and slivered onions because it may be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 6, 2012· Gills Onions, LLC

Recalled Item: 3/16" Slivered Red Onions Recalled by Gills Onions, LLC Due to Potential...

The Issue: Gills Onions is recalling diced and slivered onions because it may be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Hip Components: INSERT MOBILE "COLLEGIA" TAILLE 58*28 Recalled by Wright...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Knee Components: ROTULE "913" D=32 Recalled by Wright Medical Technology Inc...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM Recalled by...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: Mindray DPM5 Monitor Recalled by Mindray DS USA, Inc. d.b.a. Mindray North...

The Issue: Mindray has identified an issue with the DPM5 monitors where ST and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Zimmer, Inc.

Recalled Item: ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended...

The Issue: Zimmer is conducting a voluntary removal of some Zimmer A.T.S. 3000...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Inverse Humeral Cup Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Biolox¿ delta Ceramic Femoral Head Rx only Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: zimmer Anatomical Shoulder Glenoid S Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Biolox¿ Option Ceramic Femoral Head System Rx Recalled by Zimmer, Inc. Due...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing