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. 2,260 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,260 in last 12 months

Showing 4482144840 of 47,632 recalls

FoodFebruary 19, 2013· Bimbo Bakeries Usa

Recalled Item: Arnold Dutch Country 100% Whole Grain Bread Recalled by Bimbo Bakeries Usa...

The Issue: Firm has initiated a voluntary recall due to the possible presence of...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 19, 2013· Bimbo Bakeries Usa

Recalled Item: Brownberry Healthfull 45 Calories Per Slice Multigrain Bread Recalled by...

The Issue: Firm has initiated a voluntary recall due to the possible presence of...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 19, 2013· Bimbo Bakeries Usa

Recalled Item: Sara Lee 12 Grain Bread Hearty & Delicious Recalled by Bimbo Bakeries Usa...

The Issue: Firm has initiated a voluntary recall due to the possible presence of...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 19, 2013· Blue Planet Foods, Inc.

Recalled Item: Heartland Recalled by Blue Planet Foods, Inc. Due to Blue Planet products...

The Issue: Blue Planet products that contain the two recalled Dakota Specialty Milling...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 19, 2013· Bimbo Bakeries Usa

Recalled Item: Stroehmann Dutch Country 100% Whole Grain Bread Recalled by Bimbo Bakeries...

The Issue: Firm has initiated a voluntary recall due to the possible presence of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 19, 2013· Hospira Inc.

Recalled Item: Minibore Extension Set Recalled by Hospira Inc. Due to Hospira, Inc. is...

The Issue: Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2013· Trumpf Medical Systems, Inc.

Recalled Item: Helion S Exam Light or H300 The device is intended Recalled by Trumpf...

The Issue: Possible fatigue failure of the plastic joint may occur after an average use...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2013· Remel Inc

Recalled Item: Remel X/pect Flu A&B Control Swabs Recalled by Remel Inc Due to Flu A+...

The Issue: Flu A+ Control Swabs incorrectly give Flu A- results when used for quality...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 19, 2013· Tecan US, Inc.

Recalled Item: Tecan Freedom EVO with Touch Tools Suite Version 3.0 The Recalled by Tecan...

The Issue: WIth TouchTools 3.0 after the execution of a Rich User Prompt in Display and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic DPL Single Stage Venous Cannula with Metal Tip Recalled by...

The Issue: Potential for uncharacteristically rough metal edges to occur along the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 18, 2013· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The product is being recall due to the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 18, 2013· Ge Medical Systems Information T

Recalled Item: Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging...

The Issue: It was reported from a complaint that study category labels of "Prior" and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Ge Healthcare It

Recalled Item: Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Recalled...

The Issue: A software defect was discovered that causes images to be out of context...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· GE Healthcare

Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...

The Issue: Using Merge Exam in single Study Mode may result in Missing Study Record...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 60 computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 XL computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 Compact computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
DrugFebruary 15, 2013· Warner Chilcott Company LLC

Recalled Item: Femhrt (norethindrone acetate and ethinyl estradiol) tablets Recalled by...

The Issue: Chemical contamination: Firm's inspection discovered the presence of...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2013· Warner Chilcott Company LLC

Recalled Item: Femhrt (norethindrone acetate and ethinyl estradiol) tablets Recalled by...

The Issue: Chemical contamination: Firm's inspection discovered the presence of...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2013· Warner Chilcott Company LLC

Recalled Item: Jevantique (norethindrone acetate and ethinyl estradiol) tablets Recalled by...

The Issue: Chemical contamination: Firm's inspection discovered the presence of...

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

Class III — Low RiskOngoing
Refund