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. 2,371 recalls have been distributed to Maine in the last 12 months.
Showing 25181–25200 of 48,770 recalls
Recalled Item: 0.2% ROPivacaine Recalled by Avella of Deer Valley, Inc. Store 38 Due to...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine 20 mg (PHENYLephrine HCL (USP) 20 mg Recalled by Avella of...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Midazolam 1 mg/mL (Midazolam HCL (USP) 100 mg Recalled by Avella of Deer...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAGnesium 1gm in NS 100 mL (MAGnesium SULfate (USP) 1 gm Recalled by Avella...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine Sulfate Recalled by Avella of Deer Valley, Inc. Store 38 Due to...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine Sulfate Recalled by Avella of Deer Valley, Inc. Store 38 Due to...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEPARIN 12 Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MORphine 150 mg (Morphine Sulfate Recalled by Avella of Deer Valley, Inc....
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEPARIN 25 Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepiNEPHrine Bitartrate Recalled by Avella of Deer Valley, Inc. Store 38...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepiNEPHrine 8 mg (norepinephrine Bitartrate (USP) 8 mg added to Recalled...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine 40 mg (PHENYLephrine HCL (USP) 40 mg Recalled by Avella of...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2" Recalled by Teleflex...
The Issue: The incorrect plastic was used to manufacture the handles of these shears,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to In 2018, Philips...
The Issue: In 2018, Philips Respironics added foam replacement to the preventive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive...
The Issue: Incorrect use-by date on the device registration/patient file labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIQ Product Usage: Vascular Recalled by Philips Healthcare Due to The first...
The Issue: The first time an operator selects a new procedure type during a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Seven Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Alpha Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Gamma Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper Product Usage: Vascular Recalled by Philips Healthcare Due to...
The Issue: The first time an operator selects a new procedure type during a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.