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. 2,355 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,355 in last 12 months

Showing 2998130000 of 48,770 recalls

FoodFebruary 21, 2017· Give and Go Prepared Foods Corp - Finch

Recalled Item: Two-Bite Pecan Tart 9.2 oz (261g) item number 02023 Recalled by Give and Go...

The Issue: Dried weevil larvae may be present in the recalled products.

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

Class III — Low RiskOngoing
Refund
FoodFebruary 21, 2017· Give and Go Prepared Foods Corp - Finch

Recalled Item: Two-Bite Pecan Tarts Party Platter 16 x 16.2 (460g) item number 09877...

The Issue: Dried weevil larvae may be present in the recalled products.

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

Class III — Low RiskOngoing
Refund
FoodFebruary 21, 2017· Give and Go Prepared Foods Corp - Finch

Recalled Item: Two-Bite Turtle Brownie Party Platter 16 x 12.2 oz (346g) item number 09904...

The Issue: Dried weevil larvae may be present in the recalled products.

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

Class III — Low RiskOngoing
Refund
FoodFebruary 20, 2017· Grace Kennedy Foods USA LLC

Recalled Item: La Fe Papa Criollas Yellow Potato Net Wt. 14 oz. Recalled by Grace Kennedy...

The Issue: La Fe Papas Criollos may be contaminated with Listeria Monoctyogenes.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2017· Signal Medical Corporation

Recalled Item: Soft Face "No Bounce" Mallet Model/Catalog: BIO-1-1090 Recalled by Signal...

The Issue: Potential for poly tip of the mallet to come off during use. Potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Orthosoft, Inc. dba Zimmer CAS

Recalled Item: SmartTools Knee System Orthopedic Stereotaxic Instrument Recalled by...

The Issue: There has been an increase in the number of complaints regarding bent or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software updates

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.

Recalled Item: AMS-636 Recalled by Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc....

The Issue: Incorrect priming volume printed on the device package.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Gel Pads Product Recalled...

The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Pads Recalled by Terumo...

The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· CareFusion 303, Inc.

Recalled Item: MaxGuard Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the MaxGuard Extension Set due to reports of leaks...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 16 TruePoint - 3R Recalled by Siemens Medical Solutions USA Inc....

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 16 TruePoint TrueV - 4R Recalled by Siemens Medical Solutions USA...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: Potassium CHLORide added to 0.9% Sodium Chloride Recalled by Pharmedium...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: Potassium PHOSphate in 0.5% Dextrose Recalled by Pharmedium Services, LLC...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: Potassium PHOSphate added to 0.9% Sodium Chloride Recalled by Pharmedium...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: Potassium PHOSphate added to 0.9% Sodium Chloride Recalled by Pharmedium...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: VANCOMYCIN HCl 1.5g in 300 mL 5% Dextrose Injection USP Recalled by...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

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

Class II — Potential Health HazardOngoing
Refund