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. 2,499 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,499 in last 12 months

Showing 1268112700 of 48,770 recalls

Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
DrugMarch 14, 2022· Vitae Enim Vitae Scientific, Inc.

Recalled Item: TETRACAINE 1% Tetracaine HCI Injection Recalled by Vitae Enim Vitae...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Vitae Enim Vitae Scientific, Inc.

Recalled Item: PHENOBARBITAL Sodium Injection Recalled by Vitae Enim Vitae Scientific, Inc....

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Vitae Enim Vitae Scientific, Inc.

Recalled Item: PHENOBARBITAL Sodium Injection Recalled by Vitae Enim Vitae Scientific, Inc....

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Vitae Enim Vitae Scientific, Inc.

Recalled Item: PAPAVERINE HYDROCHLORIDE Injection Recalled by Vitae Enim Vitae Scientific,...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Phenylephrine HCl Injection 50 mg per 250 mL in 0.9% Sodium Chloride...

The Issue: Defective container

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Epinephrine Injection 8 mg per 250 mL in 0.9% Sodium Chloride Recalled by...

The Issue: Defective container

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Norepinephrine Bitartrate Injection 8 mg per 250 mL in 0.9% Sodium Chloride...

The Issue: Defective container

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Norepinephrine Bitartrate Injection 16 mg per 250 mL added to Recalled by...

The Issue: Defective container

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Phenylephrine HCl Injection in 0.9% Sodium Chloride Recalled by Athenex...

The Issue: Defective container

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Phenylephrine HCl Injection 40 mg per 250 mL in 0.9% Sodium Chloride...

The Issue: Defective container

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Norepinephrine Bitartrate Injection 4mg per 250 mL in 0.9% Sodium Chloride...

The Issue: Defective container

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 14, 2022· Neuralynx Inc

Recalled Item: ATLAS Stim Headbox-NK For use only with the ATLAS Neurophysiology Recalled...

The Issue: Atlas Stim Headbox (ASHB) was delivered to US customers under a premise that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2022· Sensory Medical Inc

Recalled Item: Cub 2 Enclosed Bed Canopy System Recalled by Sensory Medical Inc Due to Due...

The Issue: Due potential misuse of the product, firm is updating warnings and...

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

Class I — Serious Health HazardOngoing
DrugMarch 11, 2022· DASH Pharmaceuticals LLC

Recalled Item: Sucralfate Oral Suspension Recalled by DASH Pharmaceuticals LLC Due to...

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 DeviceMarch 11, 2022· DePuy Orthopaedics, Inc.

Recalled Item: VELYS Robotic-Assisted Solution Base Product No.: 451570100 Recalled by...

The Issue: System software v1.5.1 has a system software issue related to the Daylight...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2022· Sartorius Corporation

Recalled Item: Virus Counter Platform with Model Name VC3100 Recalled by Sartorius...

The Issue: The Virus Counter is an automated laboratory instrument that enables rapid...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2022· Abbott Vascular

Recalled Item: Plus 30 Priority Pack w/.096 RHV - WPL2122277-01 Recalled by Abbott Vascular...

The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...

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

Class II — Potential Health HazardOngoing