Garden of Life, RM-10, Organically Grown Mushrooms, 60 Vegetarian Caplets, Whole Food Dietary Supplement
Garden Of Life
Undeclared Soy.
95,018 total recalls in our database
Garden Of Life
Undeclared Soy.
During an FDA inspection the firm was notified that some of their products contains undeclared soy and Yellow #5 & #6.
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5 & #6.
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5, Green 3.
Failed Tablets/Capsules specifications; missing/broken/extra tablets within the capsules
MARKETED WITHOUT AN APPROVED NDA/ANDA: Product found to be tainted with metformin and glyburide
Failed Dissolution Specifications
Right Value Drug Stores, LLC
Product Mix-up: Incorrect Product Formulation
Wells Pharma of Houston
Lack of assurance of sterility.
Failed Impurities/Degradation Specifications
STAQ Pharma Inc. received consumer complaints related to leaking bags and other potential bag concerns. Upon investigation, they determine the source of the issue was with the bag manufacturer who released bags Lot # 134142-001A which had failed internal QC tests for leaks.
Failed pH Specifications
Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals
Failed Impurities/Degradation Specifications
Staar Surgical Company
Their is a potential that intraocular implant devices may not meet specifications.
Integra LifeSciences
Defect in the outer packaging of the Cranial Access Kits. can cause the packaging to split without any additional forces outside compromising the sterility of the device
Elekta has identified that if the microswitch within the middle arm is incorrectly setup, there is a potential for an uncontrolled extension of iViewGT / XVI detector arms. When the detector arm is fully deployed there is no risk of uncontrolled extension.
Elekta has identified that if the microswitch within the middle arm is incorrectly setup, there is a potential for an uncontrolled extension of iViewGT / XVI detector arms. When the detector arm is fully deployed there is no risk of uncontrolled extension.
Wilson-Cook Medical
Nonconforming devices while manufactured correctly, do not comply to their design requirements. Potential harms associated with balloon detachment are endoscopic retrieval of an impacted or non-impacted object, bleeding caused by the retrieval device, or the incident can occur without injury and the object is left to pass naturally.
Incorrect bonding material used for assembly of the catheter, may fail, resulting in detachment of component parts, broken components, or leakage. This breakage may result in delay of procedure