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. 2,464 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,464 in last 12 months

Showing 2134121360 of 50,117 recalls

FoodJuly 11, 2019· Wismettac Asian Foods, INC

Recalled Item: Shirakiku FISH CAKE IKA MAKI SK F Recalled by Wismettac Asian Foods, INC Due...

The Issue: Fish Cake items contain possible contaminating undeclared egg, milk and...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 11, 2019· Wismettac Asian Foods, INC

Recalled Item: Shirakiku FISH CAKE GOBO MAKI SK F: 20/ 150G Recalled by Wismettac Asian...

The Issue: Fish Cake items contain possible contaminating undeclared egg, milk and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 11, 2019· Merge Healthcare, Inc.

Recalled Item: Merge PACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to Potential...

The Issue: Potential for prior thumbnails to not display in reverse chronological order...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2019· Merge Healthcare, Inc.

Recalled Item: Merge OrthoPACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to...

The Issue: Potential for prior thumbnails to not display in reverse chronological order...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 1000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There is a potential for low discordant progesterone results on a subset of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There is a potential for low discordant progesterone results on a subset of...

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

Class II — Potential Health HazardOngoing
DrugJuly 10, 2019· LNK International, Inc.

Recalled Item: Equate Night-time Sleep Aide (Diphenhydramine HCl) Recalled by LNK...

The Issue: Microbial contamination of non-sterile product

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Drospirenone and Ethinyl Estradiol Tablets Recalled by Jubilant Cadista...

The Issue: Failed dissolution specifications : failed results at the 3-month stability...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Phadia Ab

Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...

The Issue: code 7-102 Liquid Sensor Error

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...

The Issue: The action has been initiated to address reports of burst balloons which...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 9, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...

The Issue: The action has been initiated to address reports of burst balloons which...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 9, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...

The Issue: The action has been initiated to address reports of burst balloons which...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...

The Issue: The action has been initiated to address reports of burst balloons which...

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

Class I — Serious Health HazardOngoing
FoodJuly 9, 2019· FLOWERS FOODS

Recalled Item: Flowers Enriched Rolls Recalled by FLOWERS FOODS Due to The products have...

The Issue: The products have the potential to contain small pieces of hard plastic...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 9, 2019· FLOWERS FOODS

Recalled Item: Flowers Bratwurst Buns 12 CT Recalled by FLOWERS FOODS Due to The products...

The Issue: The products have the potential to contain small pieces of hard plastic...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 9, 2019· FLOWERS FOODS

Recalled Item: Dinner Rolls sold under the brand names of Laura Lynn Recalled by FLOWERS...

The Issue: The products have the potential to contain small pieces of hard plastic...

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

Class II — Potential Health HazardOngoing
Refund