Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,392 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,392 in last 12 months

Showing 2310123120 of 48,770 recalls

Medical DeviceNovember 16, 2018· LivaNova USA Inc

Recalled Item: The LivaNova VNS Therapy System Recalled by LivaNova USA Inc Due to Lead...

The Issue: Lead impedance values reported by the affected VNS generator will be higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2018· LivaNova USA Inc

Recalled Item: Cyberonics VNS Therapy AspireSR Recalled by LivaNova USA Inc Due to This...

The Issue: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was...

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

Class II — Potential Health HazardOngoing
DrugNovember 16, 2018· CAO Group, Inc.

Recalled Item: BeeGentle Honey Flavored Topical Anesthetic Recalled by CAO Group, Inc. Due...

The Issue: cGMP violations noted during the firm's most recent inspection.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2018· CAO Group, Inc.

Recalled Item: fas.TRACT Coagulative Hemostatic Gel Recalled by CAO Group, Inc. Due to cGMP...

The Issue: cGMP violations noted during the firm's most recent inspection.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2018· CAO Group, Inc.

Recalled Item: SHEER DesenZ Desensitizing Treatment Recalled by CAO Group, Inc. Due to cGMP...

The Issue: cGMP violations noted during the firm's most recent inspection.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2018· CAO Group, Inc.

Recalled Item: FastStat Topical Hemostat Introductory Kit Recalled by CAO Group, Inc. Due...

The Issue: cGMP violations noted during the firm's most recent inspection.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 16, 2018· Chukar Cherry Company

Recalled Item: Ultra Dark Chocolate Cocoa Pecans Recalled by Chukar Cherry Company Due to...

The Issue: Product contains unintentional presence of milk and therefore milk was not...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 16, 2018· Chukar Cherry Company

Recalled Item: Ultra Dark Chocolate Amaretto Rainier Cherries Recalled by Chukar Cherry...

The Issue: Product contains unintentional presence of milk and therefore milk was not...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 16, 2018· Agropur MSI Ingredients LLC

Recalled Item: Jay Robb Unflavored Egg White Protein Recalled by Agropur MSI Ingredients...

The Issue: JayRobb Unflavored Egg White Protein Product is being recalled due to...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 16, 2018· Chukar Cherry Company

Recalled Item: Organic Ultra Dark Orange Chocolate Tart Cherries Recalled by Chukar Cherry...

The Issue: Product contains unintentional presence of milk and therefore milk was not...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 16, 2018· Chukar Cherry Company

Recalled Item: Ultra Dark Chocolate Black Forest Cherries Recalled by Chukar Cherry Company...

The Issue: Product contains unintentional presence of milk and therefore milk was not...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 16, 2018· Chukar Cherry Company

Recalled Item: Organic Ultra Dark Vanilla Chocolate Rainier Cherries Recalled by Chukar...

The Issue: Product contains unintentional presence of milk and therefore milk was not...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2018· 4Patriots, LLC

Recalled Item: 4Patriots Chicken a la King CONTAINS: Wheat Recalled by 4Patriots, LLC Due...

The Issue: Milk not declared on product label.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 15, 2018· Fresenius Kabi USA, LLC

Recalled Item: SODIUM CHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Labeling Not Elsewhere Classified: Fresenius Kabi is taking this action due...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 15, 2018· Fresenius Kabi USA, LLC

Recalled Item: SODIUM CHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Labeling Not Elsewhere Classified: Fresenius Kabi is taking this action due...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 15, 2018· Prollenium Medical Technologies Inc.

Recalled Item: Revanesse Versa Recalled by Prollenium Medical Technologies Inc. Due to...

The Issue: Labeling error. The product is labeled with an 18 month expiration date,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2018· Covidien LLC

Recalled Item: Covidien Emprint Standard Percutaneous Antenna with Thermosphere Technology...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2018· Howmedica Osteonics Corp.

Recalled Item: HydroSet XT Injectable HA Bone Cement Recalled by Howmedica Osteonics Corp....

The Issue: Incorrect expiry date of 17-Dec-19 Correct expiry date is 11-Aug-19

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2018· Covidien LLC

Recalled Item: Covidien Emprint Long Percutaneous Antenna with Thermosphere Technology...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2018· Covidien LLC

Recalled Item: Covidien Emprint Short Percutaneous Antenna with Thermosphere Technology...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing