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 21741–21760 of 48,770 recalls
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Hook/Triangle Blade Kit Recalled by Stryker GmbH Due to The...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Hook/Triangle Blade Kit Recalled by Stryker GmbH Due to The...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Relpax (eletriptan HBr) 40 mg Recalled by Pfizer Inc. Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength: an artwork error on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips EPIQ and Affiniti Ultrasound Systems with software version 4.0:...
The Issue: There is a potential that the image of one patient could get unexpectedly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR and Argyle acute hemodialysis catheters Recalled by COVIDIEN LLC...
The Issue: The priming volume values printed on the MAHURKA and Argyle acute catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliBridge System configured with a regional setting which uses...
The Issue: Infusion Pump Data Storage Accuracy-Data from the BBraun Space LAN or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Patient Information Center iX configured with a regional setting...
The Issue: Infusion Pump Data Storage Accuracy-Data from the BBraun Space LAN or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral...
The Issue: The sensor's look up calibration files were incorrectly programmed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDROmorphone 20 mg/100 mL Injectable Solution Recalled by Advanced Pharma...
The Issue: Sub-potency
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dried whole elderberry Recalled by Oregons Wild Harvest Inc Due to Dried...
The Issue: Dried whole Elderberries are recalled due to glass fragments contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Inovo Single Luman Conserver Product Usage: This device is intended Recalled...
The Issue: The pressure gauge (manometer) may dislodge from the threaded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquarius D13S319 Plus Deletion Probe Recalled by Cytocell Ltd. Due to There...
The Issue: There is an error in the chromomap on the package insert.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...
The Issue: There is the potential that a HeatWrap could include cells that have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLOPATH Balloon Expandable TransFemoral System Recalled by Terumo Medical...
The Issue: There is a potential for dislodgement of the tip from the outer diameter of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.