Quallent Duloxetine Delayed-Release Capsules 60 mg Recall Expanded for Impurity Above FDA Interim Lm
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.
613 recalls tagged with “poisoning risk”.
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.




This recall involves 100% pure gum spirits of turpentine bottles. The 4-ounce, clear glass bottles are round and have a label with "Georgia Pine Gum Spirits of Turpentine" and "Diamond G Forest Products" printed on it.
Failed Stability Specifications: Out of specification results was observed in Induction Port during the analysis of Particle size distribution at the 12-month time point.
Failed Dissolution Specifications: low dissolution results
Potential contamination with Listeria monocytogenes
Potential contamination with Listeria monocytogenes
DJO Surgical recall affects 439 AltiVate Reverse Glenoid Tray kits distributed across 26 states and Puerto Rico. A reamer in the kit may kick or bind during use. Patients and clinicians should stop using the device and follow manufacturer instructions.
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

This recall involves SPPTTY kids bicycles. The bicycles are pink with brown seat covers, brown handlebars, brown pedals and brown baskets and were sold in 14-inch and 18-inch sizes. The brand "SPPTTY" and "New Sport Bike" are printed on the downtube.

Lack of pasteurization and sanitation records
Lack of pasteurization and sanitation records