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 2270122720 of 48,770 recalls

FoodJanuary 23, 2019· THRIVE MARKET

Recalled Item: Thrive Market Non-GMO Crunchy Almond Butter 16 oz. SKU/Recalled by THRIVE...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 22, 2019· Twenty-First Century Healthcare, Inc

Recalled Item: Good Neighbor Pharmacy Recalled by Twenty-First Century Healthcare, Inc Due...

The Issue: 21st Century HealthCare, Inc. is recalling Good Neighbor Pharmacy brand Co...

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

Class III — Low RiskOngoing
Refund
FoodJanuary 22, 2019· Twenty-First Century Healthcare, Inc

Recalled Item: Good Neighbor Pharmacy Recalled by Twenty-First Century Healthcare, Inc Due...

The Issue: 21st Century HealthCare, Inc. is recalling Good Neighbor Pharmacy brand Co...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 19, 2019· GE Healthcare, LLC

Recalled Item: Revolution CT scanners Product Usage: The system is intended for head...

The Issue: Additional low dose radiation exposure.

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

Class II — Potential Health HazardOngoing
DrugJanuary 18, 2019· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Alprazolam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurities/Degradation Specifications: Elevated levels of a known...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2019· Prinston Pharmaceutical Inc

Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2019· Mylan Pharmaceuticals Inc.

Recalled Item: Fexofenadine HCl Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: Related compound results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2019· Prinston Pharmaceutical Inc

Recalled Item: Irbesartan Tablets 300 mg 90 count Rx only Manufactured by: Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2019· Prinston Pharmaceutical Inc

Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2019· Prinston Pharmaceutical Inc

Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2019· Prinston Pharmaceutical Inc

Recalled Item: Irbesartan and HydrochlorothiazideTablets Recalled by Prinston...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 18, 2019· Bellus Medical

Recalled Item: SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG - Recalled...

The Issue: Cosmetic Kit was packaged with a mislabel medical product.

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

Class II — Potential Health HazardOngoing
FoodJanuary 17, 2019· Friendly Fruit Market dba Sid Wainer & Son

Recalled Item: JANSAL VALLEY Cocoa Dusted Chocolate Covered Almonds Recalled by Friendly...

The Issue: Product contains undeclared sesame seeds.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 17, 2019· CryoLife, Inc.

Recalled Item: On-X Aortic Heart Valve with Anatomic Sewing Ring Product Usage: Recalled by...

The Issue: On-X Valve was mislabeled with the incorrect serial number.

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

Class II — Potential Health HazardOngoing
DrugJanuary 16, 2019· KRS Global Biotechnology, Inc

Recalled Item: NORepinephrine 16 mg added to 0.9% Sodium Chloride (PF) Recalled by KRS...

The Issue: Labeling: Label mix-up

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2019· KRS Global Biotechnology, Inc

Recalled Item: NORepinephrine 4 mg added to 5% Dextrose 250 mL Bag (PF) Recalled by KRS...

The Issue: Labeling: Label mix-up

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2019· Polymer Technology Systems, Inc.

Recalled Item: CHOL+HDL+GLU test strips Recalled by Polymer Technology Systems, Inc. Due to...

The Issue: Some lots of test strips do not fit tightly into the optical block, and may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2019· Polymer Technology Systems, Inc.

Recalled Item: Lipid Panel test strips (as a component of smart bundles) Recalled by...

The Issue: Some lots of test strips do not fit tightly into the optical block, and may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2019· Polymer Technology Systems, Inc.

Recalled Item: Lipid Panel test strips Recalled by Polymer Technology Systems, Inc. Due to...

The Issue: Some lots of test strips do not fit tightly into the optical block, and may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2019· Carolina Liquid Chemistries

Recalled Item: CAROLINA(R) LIQUID CHEMISTRIES CORP. ETHA RGT. KIT Recalled by Carolina...

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

Class III — Low RiskOngoing