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. 2,499 recalls have been distributed to Maine in the last 12 months.
Showing 12561–12580 of 48,770 recalls
Recalled Item: Instructions for Use Recalled by Medtronic Inc Due to Errors and...
The Issue: Errors and inconsistencies that were identified in the Instruction for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dragonfly OpStar Imaging Catheter Recalled by Abbott Vascular Due to There...
The Issue: There is a potential that the proximal marker may separate from the imaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evans Wedge Disposable Trials Recalled by restor3d Inc. Due to During...
The Issue: During re-work of disposable instruments to relabel for 4-year shelf-life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Sterile Double Ended Trial Kit Recalled by restor3d Inc. Due to Product...
The Issue: Product labeled incorrectly. The lot was labeled with Small footprint when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evans Wedge Disposable Trials Recalled by restor3d Inc. Due to During...
The Issue: During re-work of disposable instruments to relabel for 4-year shelf-life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mickey Mouse Hand Sanitizer Recalled by Best Brands Consumer Products, Inc....
The Issue: Chemical Contamination; FDA analysis found product to contain methanol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Mandalorian Hand Sanitizer Recalled by Best Brands Consumer Products,...
The Issue: Chemical Contamination; FDA analysis found product to contain benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pink Pussycat SENSUAL ENHANCEMENT capsule Recalled by Pink Toyz Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IDArubicin Hydrochloride Injection USP 5gm/5mL (1mg/mL) for intravenous use...
The Issue: Presence of Particulate Matter: Product was found to contain silica and iron...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The device is a whole-body CT x-ray system. The acquired Recalled by Philips...
The Issue: Three software issues affecting incorrect image display, error interpreting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preferred Pharmaceuticals Recalled by Preferred Pharmaceuticals, Inc. Due to...
The Issue: Out of specification results observed in dissolution during long term...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MedMinder Medication Dispenser- Intended to serve as a medication reminder...
The Issue: Discontinuation of the Emergency Alert watch or pendant will no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Toe II Intramedullary Arthrodesis Implant Recalled by Stryker GmbH Due...
The Issue: The nickel-sensitivity statement on the outer carton may be partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific Recalled by...
The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific Recalled by...
The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products LH Reagent Pack Product Code: 1350198...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Prolactin Reagent Pack Product Code:...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products FSH Reagent Pack- IVD 1931922 Recalled by...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Uretero-reno videoscope Recalled by Olympus Corporation of the...
The Issue: The bending section of the URF-V2 may crack, resulting in an abnormal shape...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Recalled by Arthrex, Inc. Due to Products do not meet length and...
The Issue: Products do not meet length and diameter specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.