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. 2,266 recalls have been distributed to Maine in the last 12 months.
Showing 47201–47220 of 48,770 recalls
Recalled Item: Protein Wave 15 grams of protein Recalled by Protica, Inc Due to Product not...
The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Protein Shots Recalled by Protica, Inc Due to Product not sufficiently...
The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Luigi's Real Italian Ice Birthday Cake 6 FL OZ cups Recalled by J & J Snack...
The Issue: Luigi's Real Italian Ice Birthday Cake Flavor is mislabeled as "Dairy-Free".
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is...
The Issue: Shipped with incorrect software
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System Recalled by Karl...
The Issue: The recall was initiated because Karl Storz has confirmed that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275...
The Issue: Philips SureSigns VSi/VS2+ patient monitors may not be properly secured and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stockert Heater-Cooler 3T Recalled by Sorin Group USA, Inc. Due to On August...
The Issue: On August 15, 2012, Sorin informed consignees via letter of changes made to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDROmorphone HCl Injection Recalled by Hospira Inc. Due to Superpotent...
The Issue: Superpotent (Single Ingredient) Drug: The prefilled cartridge unit has been...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Capex Shampoo (fluocinolone acetonide) Recalled by Galderma Laboratories,...
The Issue: Subpotent; fluocinolone acetonide.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Choletec - Kit for the Preparation of Technetium Tc 99m Mebrofenin Recalled...
The Issue: Presence of Particulate Matter; potential for charcoal particulates
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prometh VC Plain Recalled by Actavis Mid Atlantic LLC Due to...
The Issue: Impurities/Degradation Products: Recalled lots do not meet room temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prometh VC with Codeine Cough Syrup Recalled by Actavis Mid Atlantic LLC Due...
The Issue: Impurities/Degradation Products: Recalled lots do not meet room temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: THERA PEARL 3-in-1 BREAST THERAPY Recalled by Lansinoh Laboratories Inc Due...
The Issue: The Spanish translation on the Instructions for Use (IFU) insert and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JUGGERKNOT IN¿GUIDE PUNCH Recalled by Biomet, Inc. Due to Investigation...
The Issue: Investigation found that the current design of the product allows the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software for Vitrea Recalled by Vital Images, Inc. Due to Vital Images has...
The Issue: Vital Images has found two potential errors in calcium score values in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare became...
The Issue: GE Healthcare became aware of a potential issue related to incorrect image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray A3 Anesthesia Delivery System Manufactured in China for Mindray...
The Issue: Mindray has identified the potential for a system leak resulting an issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progel Pleural Air Leak Sealant Recalled by Neomend Inc Due to Product was...
The Issue: Product was distributed with an incorrect expiration date. Product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray A5 Anesthesia Delivery System Manufactured in China for Mindray...
The Issue: Mindray has identified the potential for a system leak resulting an issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: intraKID Lot 658 with a Best By date of 12/12 Recalled by Drucker Labs LP...
The Issue: After extensive testing and investigation, Drucker Labs has determined that...
Recommended Action: Do not consume. Return to store for a refund or discard.