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. 1,670 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,670 in last 12 months

Showing 4098141000 of 47,632 recalls

Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F160NR High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F18Nre Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F200NR High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F180NR High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator used Model numbers: M3535A...

The Issue: HeartStart MRx Defibrillator Monitor therapy connection could experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F200NRe High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Focus Diagnostics Inc

Recalled Item: Simplexa Flu AlB & RSV Direct Assay Kits Recalled by Focus Diagnostics Inc...

The Issue: Focus Diagnostics initiated the recall of the certain Simplexa Flu AlB & RSV...

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

Class II — Potential Health HazardOngoing
FoodFebruary 4, 2014· Popcorn Factory, The

Recalled Item: Candy coated popcorn shaped into a heart weighing 1.5 ounces Recalled by...

The Issue: The Nutrition Facts and allergen label was not applied individual popcorn...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2014· Aaron Industries Inc

Recalled Item: Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid (dextromethorphan...

The Issue: Presence of Precipitate: Recall is due to complaints of a white substance,...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 4, 2014· Actavis Elizabeth LLC

Recalled Item: Alprazolam Extended-Release Tablets Recalled by Actavis Elizabeth LLC Due to...

The Issue: Failed Dissolution Specifications: Product did not meet specification...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 3, 2014· Innovative Sterlization Technologies LLC

Recalled Item: OneTray Sealed Sterilization Containers Product Usage: A rigid sterilization...

The Issue: The wrong sterilization time was on the label. The label lists Steam Gravity...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Citation TMZF HA 132 degrees Neck Angle Recalled by Stryker Howmedica...

The Issue: Stryker received a report from the field indicating that a citation TMZF HA...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Altasource LLC dba Meta Labs LLC

Recalled Item: Hot Ice Recalled by Altasource LLC dba Meta Labs LLC Due to Firm is not...

The Issue: Firm is not registered as a drug manufacturer.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Altasource LLC dba Meta Labs LLC

Recalled Item: Mega-Gen His Personal Lubricant Recalled by Altasource LLC dba Meta Labs LLC...

The Issue: Firm is not registered as a drug manufacturer.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Siemens Medical Solutions Diagnostics

Recalled Item: IMMULITE 2000 Recalled by Siemens Medical Solutions Diagnostics Due to There...

The Issue: There is a potential for incorrect results to be reported from processing of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Altasource LLC dba Meta Labs LLC

Recalled Item: Nice-En-Smooth Berry Burst Recalled by Altasource LLC dba Meta Labs LLC Due...

The Issue: Firm is not registered as a drug manufacturer.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Altasource LLC dba Meta Labs LLC

Recalled Item: Amo-O Herbal Stimulator Recalled by Altasource LLC dba Meta Labs LLC Due to...

The Issue: Firm is not registered as a drug manufacturer.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Hospira Inc.

Recalled Item: The GemStar Power Supply is an accessory for the GemStar Recalled by Hospira...

The Issue: The GemStar Infusion pump may not receive direct current (DC) power from the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2014· Hospira Inc.

Recalled Item: The GemStar Power Supply is an accessory for the GemStar Recalled by Hospira...

The Issue: The GemStar Infusion pump may not receive direct current (DC) power from the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 31, 2014· Bock,Otto,Orthopedic Ind,Inc

Recalled Item: Otto Bock Aerial and Aerial Active Wheelchair Cushions. Material numbers:...

The Issue: Otto Bock is recalling all Aerial and Aerial Active Wheelchair Cushions from...

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

Class II — Potential Health HazardOngoing