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 2716127180 of 27,655 recalls

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 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· 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· 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· 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 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· 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 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
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical NUVO LITE MODEL 525 OCSI Recalled by Nidek Medical Products...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical NUVO LITE MODEL 520 STD Recalled by Nidek Medical Products Inc...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical NUVO LITE MODEL 925 OCSI Recalled by Nidek Medical Products...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical M5C5/ MARK5 NUVO/STD Recalled by Nidek Medical Products Inc...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical M5C5/ MARK5 NUVO/OCSI Recalled by Nidek Medical Products Inc...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical MARK5 NUVO 8 /OCSI Recalled by Nidek Medical Products Inc Due...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical MARK5 NUVO / M5C5 Recalled by Nidek Medical Products Inc Due...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical NUVO LITE MODEL 925 OCSI Recalled by Nidek Medical Products...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical MARK5 NUVO 8 STD Recalled by Nidek Medical Products Inc Due to...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 30, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray...

The Issue: During regular product monitoring, firm became aware of a potential issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: ABG II Modular Hip Stem Stryker Howmedica Osteonics Corp. Mahwah Recalled by...

The Issue: Stryker has updated the instruction for use (IFU) (product correction)for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Rejuvenate Modular Stems Stryker Ireland Carrigtwohill Industrial Estate...

The Issue: Stryker has updated the instruction for use (IFU) (product correction)for...

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

Class II — Potential Health HazardOngoing