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. 1,068 recalls have been distributed to Maine in the last 12 months.
Showing 11481–11500 of 48,770 recalls
Recalled Item: Systane Zaditor Recalled by Mckesson Medical-Surgical Inc. Corporate Office...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aspirin and Extended-Release Dipyridamole Capsules Recalled by Glenmark...
The Issue: Failed Tablet/Capsule Specification : Capsule breakage
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Alcohol Prep Pads Recalled by Mckesson Medical-Surgical Inc....
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Telmisartan and Hydrochlorothiazide Tablets USP Recalled by Glenmark...
The Issue: Defective Container: Recall of these batches has been initiated due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Naphcon A eye drops Recalled by Mckesson Medical-Surgical Inc. Corporate...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Systane Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Debrox Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrogen Peroxide Topical Solution USP Recalled by Vi-Jon, LLC Due to Cross...
The Issue: Cross Contamination With Other Products: Product is cross contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HeartWare Ventricular Assist Device (HVAD) System Batteries Recalled by...
The Issue: Battery performance issues. Battery electrical faults render it unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use Recalled by...
The Issue: Falsely Elevated Atellica CH Microalbumin_2 (¿ALB_2) Results due to Reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Genesis II Non-Porous Tibial Baseplate Size 5 Right Recalled by Smith &...
The Issue: The product was mispackaged (swapped). The devices within the inner tray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Description/Item: ChemoLock Bag Spike Recalled by ICU Medical, Inc....
The Issue: Ports have a potential for unintended disconnection, inability to connect to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-C6 Intensive Care Ventilator Recalled by Hamilton Medical AG Due to...
The Issue: Ventilator status indicator board can become loose, which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Description/Item: ChemoLock Vial Spike Recalled by ICU Medical, Inc....
The Issue: Ports have a potential for unintended disconnection, inability to connect to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Stream Irrigation System (Catalog No. 5551000) and X-Stream Irrigation...
The Issue: The device may potentially cause a fire, leading to a safety risk.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Euphoria Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.