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. 2,329 recalls have been distributed to Maine in the last 12 months.
Showing 37181–37200 of 48,770 recalls
Recalled Item: 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Terumo CVS is implementing field correction activities to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit Recalled by Mission...
The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit with Sunscreen Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ULTRA-FAST FIX Knot Pusher Suture Cutters Product Number: 72201537 Intended...
The Issue: Sterility of device maybe compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Portal¿ NOTC and VNG Recalled by Neuro Kinetics, Inc. Due to complaints of...
The Issue: complaints of system malfunction and unintended, sudden movement at start...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRI Femoral Impactor Block for knee prosthesis surgery. Orthopedic Manual...
The Issue: Potential for uncured adhesive between the metal threaded insert and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azithromycin Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to cGMP...
The Issue: cGMP Deviations: This recall is a result of the original manufacturer's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azithromycin 500 mg tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to...
The Issue: cGMP Deviations: This recall is a result of the original manufacturer's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ortho-Cept (0.15 mg desogestrel and 0.03 mg ethinyl estradiol) tablets...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EasyLink Data Management System Recalled by Siemens Healthcare Diagnostics,...
The Issue: System Limitations and Software Issues related to the following features:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: HeartWare has received complaints relating to damage or bent connection pins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortical Screw for M/DN Intramedullary Fixation. Metaphyseal/Diaphyseal Nail...
The Issue: The entire scope of 4.5mm Cortical Screws listed as compatible with the M/DN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lerner Laboratories Mucolexx Recalled by Richard-Allan Scientific Company...
The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mucolytic Agent 1 pint/473 ml Recalled by Richard-Allan Scientific Company...
The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product...
The Issue: Failures of the splice repair kit if exposed to excessive force.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adrucil (fluorouracil injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Presence of Particulate Matter: Black particulate matter was identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KABIVEN [(3.9%) Lipid Injectable Emulsion with (3.1%) Amino Acids and...
The Issue: Labeling: Label Error on Declared Strength: Labeled 3.1% Amino Acids but...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Alcon Custom Pak. The Alcon Customer Pak is an Recalled by Alcon...
The Issue: The supplier of the Devon Light Glove, a component of the Alcon Custom PAK,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raw Pine Nuts sold in the following brands and package Recalled by Waymouth...
The Issue: Waymouth Farms is recalling Raw Pine Nuts because they have the potential to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Custom Surgical Kits containing Medtronic Covidien Devon(TM) Light Gloves:...
The Issue: Surgical kits contain Medtronic Covidien Devon(TM) Light Gloves which were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.