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. 2,520 recalls have been distributed to Maine in the last 12 months.
Showing 9741–9760 of 48,770 recalls
Recalled Item: Allergy Relief Recalled by L. Perrigo Company Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by L. Perrigo Company Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy Relief Recalled by L. Perrigo Company Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by L. Perrigo Company Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Picnic Recalled by L. Perrigo Company Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy Recalled by L. Perrigo Company Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Non-Drowsy Allergy Relief Recalled by L. Perrigo Company Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy ALLER-FEX Recalled by L. Perrigo Company Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: aller-ease Recalled by L. Perrigo Company Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Zone2 Topical Analgesic Recalled by HTO Nevada, Inc. Due to cGMP...
The Issue: cGMP Deviation: Raw material recalled by repackager, due to discoloration of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: New & Improved Blue Gel Anesthetic Recalled by HTO Nevada, Inc. Due to cGMP...
The Issue: cGMP Deviation: Raw material recalled by repackager, due to discoloration of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FreeStyle Libre 3 App Recalled by Abbott Diabetes Care, Inc. Due to If using...
The Issue: If using affected glucose monitoring app on Android 13 Operating System,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal SafeLiner Suction Canister Recalled by DeRoyal Industries Inc Due to...
The Issue: The reason for the voluntary recall is due to shrinkage of the canister lid....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tacrolimus Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Presence of Foreign Tablets/Capsules: Presence of one Tacrolimus 1 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic Grafton DBF Inject: a) GRAFTON T50303 DBF INJECT 3CC Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Matrix: a) DBM S42200 GRAFTON 2.5CMX10CM 2EA MATRIX...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Crunch a) DBM S44105 GRAFTON 5CC CRUNCH Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic XPANSE Bone Insert: a) DBM T600106 XPANSE SMALL-C 6 Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Gel: a) DBM S41120 GRAFTON GEL 1CC Recalled by Medtronic...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Orthoblend: a) DBM S44125 5CC ORTHOBLEND LARGE DEFECT...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.