Product is recalled due to potential mold growth contamination.
All Recalls
95,114 total recalls in our database
Diamond Shruumz Gummies - Micro Dose Sour Peach Apple UPC 755003861386
Prophet Premium Blends
Toxic levels of muscimol
Possible contamination with Listeria monocytogenes
Possible contamination with Listeria monocytogenes
Possible contamination with Listeria monocytogenes
Product is missing the ingredient TongKat Ali and has additional Rhodiola Rosea
Possible contamination with Listeria monocytogenes
Product is recalled due to potential mold growth contamination.
Possible contamination with Listeria monocytogenes
Possible contamination with Listeria monocytogenes
Possible contamination with Listeria monocytogenes
Possible contamination with Listeria monocytogenes
Presence of Particulate Matter: Complaint received of a glass particle in the vial.
Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.
SoloVital
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared Diclofenac and Omeprazole.
Failed Dissolution Specifications
Glenmark, Azelaic Acid Gel, 15 %, 50 grams, Rx only, Manufactured by: Glenmark Pharmaceuticals Limited, Colvale-Bardez, Goa, 403513, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, NDC 68462-626-52.
Glenmark Pharmaceuticals Inc., USA
CGMP Deviations
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled as 0.125 mg instead of 0.25 mg. The blister strips inside the product carton reflect the correct strength of 0.25 mg.
Defective container: unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
There are two software bug issues with the analyzer. Issue 1: When a dedicated rack is reserved for calibration, after a calibration test has been placed and completed, the same rack may be used to place both a patient order and a calibration order. When a patient sample and a non-barcoded calibrator tube is processed on the rack, the calibration result will be reported as a patient result. Issue 2: calibration with expired calibrator. They both may cause erroneous patient results, but the probability of serious adverse health consequences or death is unlikely.
SOFT-VU KUMPE 5F X 40CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732702
Angiodynamics
Mislabeled. The shelf-box labeling (unit of sale) is accurate for the packaged devices, however the inner pouch label may contain information for a different model (catheter length)