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. 2,524 recalls have been distributed to Maine in the last 12 months.
Showing 9261–9280 of 48,770 recalls
Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...
The Issue: There is a potential that valve assemblies will not open. preventing fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...
The Issue: There is a potential that valve assemblies will not open. preventing fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...
The Issue: There is a potential that valve assemblies will not open. preventing fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...
The Issue: There is a potential that valve assemblies will not open. preventing fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...
The Issue: There is a potential that valve assemblies will not open. preventing fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...
The Issue: There is a potential that valve assemblies will not open. preventing fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...
The Issue: There is a potential that valve assemblies will not open. preventing fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspira Valve Repair Kit Recalled by Merit Medical Systems, Inc. Due to There...
The Issue: There is a potential that valve assemblies will not open. preventing fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...
The Issue: There is a potential that valve assemblies will not open. preventing fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo LNCS TC-I SpO2 Recalled by Masimo Corporation Due to TC-I tip clip...
The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo RD Set TC-I SpO2 Adult Reusable Ear Sensor Recalled by Masimo...
The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo LNCS TC-I SpO2 Recalled by Masimo Corporation Due to TC-I tip clip...
The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo LNOP TC-I SpO2 Recalled by Masimo Corporation Due to TC-I tip clip...
The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Patch 5% Recalled by Bryant Ranch Prepack, Inc. Due to Labeling:...
The Issue: Labeling: Typographical error on the upper left-hand side of the box and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Multiple Vitamin B Capsules Recalled by Euro-Pharma Due to Undeclared Allergen
The Issue: undeclared allergen (milk)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fyremadel (ganirelix acetate) injection Recalled by Sun Pharmaceutical...
The Issue: Presence of Particulate Matter: A piece of glass was found in a prefilled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Patient Information Center iX Recalled by Philips North America Due to...
The Issue: During extended operation of the MX40 with the PIC iX, the DHCP (Dynamic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Single Use Distal Cover Model Number MAJ-2315 used with Recalled by...
The Issue: The Single Use Distal Cover MAJ-2315 may cause mucosal injury and/or become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile custom surgical procedure packs (1) 89-10529.04 Recalled by DeRoyal...
The Issue: The custom procedure packs contain light handle covers that have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile custom surgical procedure packs: (1) 89-10507.02 Recalled by DeRoyal...
The Issue: The custom procedure packs contain light handle covers that have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.