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. 2,265 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,265 in last 12 months

Showing 4818148200 of 48,770 recalls

DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 70% Dextrose Injection USP Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 1.5% Glycine Irrigation Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 4, 2012· Snyder's - Lance Inc.

Recalled Item: Tom's Bacon Cheddar Fries Recalled by Snyder's - Lance Inc. Due to...

The Issue: Product contains undeclared certified colors (Yellow #6, Red #40, Yellow#6...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 4, 2012· Stanley Security Solutions, Inc.

Recalled Item: Tabs Professional Monitor Recalled by Stanley Security Solutions, Inc. Due...

The Issue: The monitor may fail to sound an alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Stanley Security Solutions, Inc.

Recalled Item: Tabs Professional Monitor Recalled by Stanley Security Solutions, Inc. Due...

The Issue: The monitor may fail to sound an alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Stanley Security Solutions, Inc.

Recalled Item: Tabs Professional Voice + Monitor Recalled by Stanley Security Solutions,...

The Issue: The monitor may fail to sound an alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Stanley Security Solutions, Inc.

Recalled Item: Tabs Professional Voice + Monitor Recalled by Stanley Security Solutions,...

The Issue: The monitor may fail to sound an alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Stanley Security Solutions, Inc.

Recalled Item: Tabs Professional Monitor Recalled by Stanley Security Solutions, Inc. Due...

The Issue: The monitor may fail to sound an alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Scenaria CT System Software Product Usage: The Scenaria system...

The Issue: Hitachi discovered a software error in the Reconstruction Status function...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 11G X 6IN Side-Fire Needle Recalled by DePuy...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 13G X 6IN Recalled by DePuy Mitek, Inc., a...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 11G X 4IN Recalled by DePuy Mitek, Inc., a...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 13G X 4IN Side-Fire Needle Recalled by DePuy...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2012· Arrow International Inc

Recalled Item: Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R)...

The Issue: Lidstock of product does not contain chlorhexidine contraindication and...

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

Class I — Serious Health HazardOngoing
DrugMay 2, 2012· Teva Pharmaceuticals USA, Inc.

Recalled Item: Zeosa (norethindrone and ethinyl estradiol tablets USP Recalled by Teva...

The Issue: Impurities/Degradation: This recall is being carried out due to the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 1, 2012· Ben Venue Laboratories Inc

Recalled Item: Octreotide Acetate Injection Recalled by Ben Venue Laboratories Inc Due to...

The Issue: Short Fill: These products are being recalled because there is potential...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 1, 2012· Ben Venue Laboratories Inc

Recalled Item: Midazolam HCl Injection Recalled by Ben Venue Laboratories Inc Due to Short...

The Issue: Short Fill: These products are being recalled because there is potential...

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

Class II — Potential Health HazardOngoing
Refund