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 37541–37560 of 48,770 recalls
Recalled Item: 119" (302 cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 98" (249 cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Alignment Guide Recalled by Zimmer CAS Due to Zimmer CAS has...
The Issue: Zimmer CAS has determined that the potential exists for the spikes on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Librax (5 mg chlordiazepoxide HCl and 2.5 mg clidinium bromide) capsules...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlordiazepoxide HCl/Clidinium Bromide capsules Recalled by Valeant...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nifedipine Extended-Release Tablets Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: High out of specification dissolution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DeRoyal(R) Medium Specimen Retrieval Bag Recalled by DeRoyal Industries Inc...
The Issue: The firm received reports of specimen retrieval bags tearing, ripping, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraview SL Command Modules Recalled by Spacelabs Healthcare Inc Due to...
The Issue: Ultraview SL Command Modules which were upgraded with the Masimo SpO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WEBSTER HIS Catheter Recalled by Biosense Webster, Inc. Due to The Webster...
The Issue: The Webster HIS catheter, 4Pole Fixed Curve with Auto ID, is not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Well at Walgreens Maximum Strength Comfort Gel 12 FL OZ (355 mL) bottle...
The Issue: Products failed the Antimicrobial Effectiveness Test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Well at Walgreens Regular Strength Antacid Liquid Recalled by Tarmac...
The Issue: Products failed the Antimicrobial Effectiveness Test.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Well at Walgreens Regular Strength Comfort Gel Cherry Flavor Recalled by...
The Issue: Products failed the Antimicrobial Effectiveness Test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hitachi Echelon MRI System Recalled by Hitachi Medical Systems America Inc...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI System Recalled by Hitachi Medical Systems America Inc Due...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon Oval MRI System Recalled by Hitachi Medical Systems America...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASC (Breast) Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Basin Kits Recalled by Covidien LLC Due to Devon Light Gloves contain...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Devon Light Gloves Recalled by Covidien LLC Due to Devon Light...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non Sterile Subassembly: Catalog Number/Description: SA1008 NONSTERILE...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Basin Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.