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. 2,392 recalls have been distributed to Maine in the last 12 months.
Showing 21161–21180 of 27,655 recalls
Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar" Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Combo Set Case The cases hold surgical instrumentation in Recalled by...
The Issue: The lids on implant caddies within P/N 17-5000 and 19-5000 could not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temporary Total Artificial Heart (TAH-t) with Freedom Driver System by...
The Issue: SynCardia Systems, Inc. is recalling Freedom Drivers due to a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thinflap System Case The cases hold surgical instrumentation in place...
The Issue: The lids on implant caddies within P/N 17-5000 and 19-5000 could not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salto Talaris Tibial Guide Recalled by Tornier, Inc Due to Tornier has...
The Issue: Tornier has initiated a voluntary recall for the Salto Talaris Tibial Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR"* 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy Recalled by...
The Issue: The neoBLUE Instruction For Use (IFU) and Service Manuals for the neoBLUE 3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Parsippany Recalled by Biomet Spine, LLC Due to Mislabeling
The Issue: Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to A software fix...
The Issue: A software fix has been released to prevent automatic movement resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.