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. 2,562 recalls have been distributed to Maine in the last 12 months.
Showing 2461–2480 of 48,770 recalls
Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...
The Issue: Defective Container: Unable to get the solution out of the bottle as the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: niCARdipine Hydrochloride Injection Recalled by American Regent, Inc. Due to...
The Issue: Lack of sterility assurance: Product leakage around the vial neck, which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: niCARdipine Hydrochloride Injection Recalled by American Regent, Inc. Due to...
The Issue: Lack of sterility assurance: Product leakage around the vial neck, which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Hydrochloride Capsules Recalled by Preferred Pharmaceuticals,...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropivacaine Hydrochloride Injection Recalled by Amneal Pharmaceuticals, LLC...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bard¿ Single Intragastric Linton Balloon Tube Recalled by C.R. Bard Inc Due...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) Recalled by C.R....
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) Recalled by C.R. Bard...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Minnesota Four Lumen Esophagogastric Tamponade Tube Recalled by C.R....
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Blakemore Esophageal-Nasogastric Tube (Adult) Recalled by C.R. Bard Inc...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments....
The Issue: Incorrect blister labelling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test Recalled by...
The Issue: It was determined that the consumable issue may result in No Call - INT CTL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus Pro Patient Monitor Recalled by Remote Diagnostic Technologies Ltd....
The Issue: software issue that causes an error screen on a portable vital signs monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bone & Joint Restore. 180 capsules in a plastic bottle. Recalled by Optimal...
The Issue: Potential for contamination with salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL) Recalled by OurPharma LLC Due...
The Issue: Superpotent Drug: Assay/potency result for hydromorphone HCl in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number:...
The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376....
The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...
The Issue: Patient Monitor software update to address issues:1)May freeze at startup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.