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 2256122580 of 48,770 recalls

DrugFebruary 22, 2019· Golean Detox US

Recalled Item: Golean DETOX capsules Recalled by Golean Detox US Due to Undeclared Sibutramine

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 22, 2019· Akorn, Inc.

Recalled Item: Gentamicin Sulfate Ophthalmic Solution Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High Out-of-Specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2019· Ascend Laboratories LLC

Recalled Item: Tamsulosin Hydrochloride Capsules Recalled by Ascend Laboratories LLC Due to...

The Issue: Failed Dissolution Specifications: High Out-of-Specification dissolution...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 22, 2019· Asia Food Distributor

Recalled Item: Nova Salted Biscuit The product comes in a 14.08 ounce Recalled by Asia Food...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 22, 2019· GE Healthcare, LLC

Recalled Item: Integrated ECG cable with 3-lead leadwires labeled as the following:...

The Issue: The Integrated ECG cable with 3-lead leadwires can short circuit during...

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

Class III — Low RiskOngoing
DrugFebruary 21, 2019· Lannett Company Inc.

Recalled Item: Oxybutynin Chloride Recalled by Lannett Company Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 21, 2019· ArthroCare Corporation

Recalled Item: Smith&Nephew SmartStitch PerfectPasser Connector Recalled by ArthroCare...

The Issue: The voluntary recall is being initiated due to a manufacturing error...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: icumedical ChemoLock Closed Vial Spike w/Skirt Recalled by ICU Medical, Inc....

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: SetSource ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: icumedical ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: icumedical ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: icumedical Oncology Kit w/12" (30cm) Ext Set w/Spiros w/Red Cap Recalled by...

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: icumedical ChemoLock Recalled by ICU Medical, Inc. Due to There is a...

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: icumedical Oncology Kit w/12" Ext Set w/Spiros w/Red Cap Recalled by ICU...

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2019· Becton Dickinson & Co.

Recalled Item: BD Synapsys Laboratory Solutions Catalog Number:444150 Product Usage: BD...

The Issue: BD Synapsys version 2.1 allowed the potential for a test order to be...

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

Class II — Potential Health HazardOngoing
FoodFebruary 20, 2019· Meijer

Recalled Item: Meijer Ultimate Chocolate Mint Chip Cookie Cookies in clear plastic Recalled...

The Issue: Undeclared soy

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2019· Luminex Corporation

Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Through internal...

The Issue: Through internal investigation, it was discovered that a portion of side...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2019· Luminex Corporation

Recalled Item: ARIES C. difficile Assay Recalled by Luminex Corporation Due to Through...

The Issue: Through internal investigation, it was discovered that a portion of side...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2019· Luminex Corporation

Recalled Item: ARIES Flu A/B & RSV Assay Recalled by Luminex Corporation Due to Through...

The Issue: Through internal investigation, it was discovered that a portion of side...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2019· Luminex Corporation

Recalled Item: ARIES GBS Assay Recalled by Luminex Corporation Due to Through internal...

The Issue: Through internal investigation, it was discovered that a portion of side...

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

Class II — Potential Health HazardOngoing