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. 947 recalls have been distributed to Maine in the last 12 months.
Showing 42101–42120 of 48,770 recalls
Recalled Item: HydrOXYzine HCl Tablets Recalled by American Health Packaging Due to Good...
The Issue: Good Manufacturing Practices Deviations: The product has an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydrOXYzine HCl Tablets Recalled by American Health Packaging Due to Good...
The Issue: Good Manufacturing Practices Deviations: The product has an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DermOtic Oil (fluocinolone acetonide) 0.01% Ear Drops Recalled by Hill...
The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Scalp Oil)...
The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUDSON VALLEY HOMESTEAD BUSHWHACKER'S SAVORY SAUCE Recalled by Charlemagnes...
The Issue: Charlemagne's Tree Farm, Ltd. dba HUDSON VALLEY HOMESTEAD recalled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HUDSON VALLEY HOMESTEAD BUSHWHACKER'S SAVORY SAUCE Recalled by Charlemagnes...
The Issue: Charlemagne's Tree Farm, Ltd. dba HUDSON VALLEY HOMESTEAD recalled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic Select CAP Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2001US: Prevena Incision Management Customizable System Box (US-ONLY)...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1001: Prevena Peel and Place System Kit Product Usage: The Recalled by...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes CMF Battery Powered Driver Recalled by Synthes, Inc. Due to The CMF...
The Issue: The CMF Battery Powered Driver graphic case contains outlines of the Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2001: Prevena Incision Management Customizable System Box Product Usage:...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1055: Prevena Dressing Recalled by KCI USA, INC. Due to Prevena...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intersept Custom Tubing Pack which contain Select 3D or Recalled...
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1001US: Prevena Peel and Place System Kit (US-ONLY) Product Usage:...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2055: Prevena Customizable Dressing 5-Pack Product Usage: The Prevena...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1055US: Prevena Dressing Recalled by KCI USA, INC. Due to Prevena...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2055US: Prevena Customizable Dressing 5-Pack (US-ONLY) Product Usage: The...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.