Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,705 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,705 in last 12 months

Showing 4766147680 of 50,117 recalls

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· Custom Healthcare Systems, Inc.

Recalled Item: Custom Breast Biopsy Tray w/Sodium Chloride Recalled by Custom Healthcare...

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· 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· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Dry Acid Concentrate For Bicarbonate Dialysis 2.0 K...

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: 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
DrugNovember 26, 2012· Pfizer Inc.

Recalled Item: TORISEL Kit (temsirolimus) injection Recalled by Pfizer Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility; potential that a low level of endotoxins may...

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

Class III — Low RiskOngoing
Refund
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· 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
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· 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· Hospira, Inc.

Recalled Item: Nalbuphine HCl Injection Recalled by Hospira, Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Complains of a loose crimp applied to the...

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

Class II — Potential Health HazardOngoing
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· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluorouracil Topical Cream USP Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Product Lacks Stability: Out-of-specification (OOS) results were observed...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens CLINITEK Atlas Positive and Negative Control Strips for Urine...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Soft Flow Ang Wire W/L The Sarns Recalled by Terumo Cardiovascular...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak Catalog Number: 1364 Chek-Stix¿ Positive and...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Soft Flow Ang W/L The Sarns Aortic Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Sft Flow Straight Wir The Sarns Aortic Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing