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. 2,355 recalls have been distributed to Maine in the last 12 months.
Showing 28081–28100 of 48,770 recalls
Recalled Item: Accu-Chek Performa II Meter - Product Usage: a. The Accu-Chek Recalled by...
The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh¿Sorter 9tray Recalled by Tosoh Bioscience Inc Due to This recall has...
The Issue: This recall has been initiated due to a potential malfunction of the photo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh¿Automated Enzyme Immunoassay Analyzer AIA-900 Recalled by Tosoh...
The Issue: This recall has been initiated due to a potential malfunction of the photo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 5 MHz Vascular Probe Recalled by Natus Neurology Inc Due to...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 3 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe Recalled by Natus Neurology Inc...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin Group Aortic Arch Cannula Recalled by Sorin Group USA, Inc. Due to...
The Issue: Identification of excess plastic on the tip of the cannula.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra 3D Revascularization Device It is indicated for used in Recalled by...
The Issue: Penumbra has identified an issue in these four lots involving a raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NitroGlycerin 1 mg/10 mL in 5% Dextrose Inj Recalled by Advanced Pharma Inc....
The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj Recalled by Advanced Pharma...
The Issue: Subpotent Drug: found to be below the specification for labeled assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj Recalled by Advanced Pharma...
The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NitroGlycerin (1 mg/5 mL) 1 mg in 5% Dextrose Inj Recalled by Advanced...
The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NitroGlycerin 1 mg/10 mL in 5% Dextrose Inj Recalled by Advanced Pharma Inc....
The Issue: Subpotent Drug: found to be below the specification for labeled assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NitroGlycerin 100 mcg/mL QS 5% Dextrose Inj Recalled by Advanced Pharma Inc....
The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NitroGlycerin (1 mg/5 mL) 1 mg in 5% Dextrose Inj Recalled by Advanced...
The Issue: Subpotent Drug: found to be below the specification for labeled assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.