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 4526145280 of 47,632 recalls

Medical DeviceNovember 26, 2012· Custom Healthcare Systems, Inc.

Recalled Item: Custom Breast Biopsy Tray Recalled by Custom Healthcare Systems, Inc. Due to...

The Issue: Surgical procedure trays are packed with pharmaceuticals for injection that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: DBS MICROPLATE Recalled by Perkinelmer Due to Truncated V-Bottomed...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: NEONATAL TOTAL GALACTOSE KIT Product Numbers: 3029-0010 Recalled by...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: NEOGRAM AMINO ACIDS AND ACYLCARNITINES TANDEM MASS SPECTROMETRY KIT Product...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: Microplate Recalled by Perkinelmer Due to Truncated V-Bottomed Microplate...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: NEOBASE NON-DERIVATIZED MSMS KIT Product Number: 3040-001U. This tandem mass...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Dako Denmark A/S

Recalled Item: CoverStainer Slide Rack The CoverStainer Slide Rack is an accessory Recalled...

The Issue: The expected life time of the CoverStainer slide racks (CS 10330) does not...

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

Class II — Potential Health HazardOngoing
FoodNovember 23, 2012· Newman'S Own Inc.

Recalled Item: Newman's Own Lite Honey Mustard Dressing Recalled by Newman'S Own Inc. Due...

The Issue: Newman's Own Lite Honey Mustard Dressing was labeled with an incorrect back...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 21, 2012· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical Oil(SCALP OIL)...

The Issue: Subpotent; 22 month stability timepoint

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

Class III — Low RiskOngoing
Refund
DrugNovember 21, 2012· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) Recalled by Hill Dermaceuticals,...

The Issue: Subpotent; 12 month stability timepoint

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

Class III — Low RiskOngoing
Refund
DrugNovember 21, 2012· Bracco Diagnostic Inc

Recalled Item: Isovue -370 (Iopamidol) Injection 76% Recalled by Bracco Diagnostic Inc Due...

The Issue: Presence of Particulate Matter; fibers identified as cellulose and polyvinyl

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 21, 2012· Bracco Diagnostic Inc

Recalled Item: Isovue -300 (Iopamidol) Injection 61% Prefilled Recalled by Bracco...

The Issue: Presence of Particulate Matter; fibers identified as cellulose and polyvinyl

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

Class I — Serious Health HazardOngoing
Refund