Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
GF Health Products, Inc., in conjunction with OKIN America, has initiated a voluntary field correction affecting the OKIN America "DUOMAT 3" Head/Foot motor used in the manufacture of our…
Package Defect: Products may be at risk for having a slit defect on the package and that may affect the product sterility.
The LightCycler 480 algorithm used for the LightMix Zika rRT-PCR Test, EUA (catalog number 07987897001) occasionally (~1% of the time) calls a positive result for a negative sample if there…
GE Healthcare has become aware of a potential safety issue where certain Avance CS2, Avance and Amingo anesthesia devices can transition to a System Malfunction state if the lower storage…
Beckman Coulter has received and confirmed reports of an intermittent and unexpected behavior when loading new panels into a WalkAway instrument using LabPro Data Management System version…
neoBLUE blanket LED Phototherapy System distributed since release of the product in 2011 is recalled due to customer complaints regarding discoloration/ degradation of fiberoptic bundle at…
The black plastic puck on the carry bar is breaking resulting in potential for patient harm.
BD has received multiple reports of units associated with the 23 G x .75 in. BD Vacutainer Push Button Blood Collection Set with 12 in. Tubing whose lots are exhibiting separation of front…
An internal real-time stability monitoring program revealed decreased recovery of myoglobin (-20% bias) for Randox Immunoturbidimetric and Siemens Centaur Classic methods and CKMB (-21%…
It has been discovered that during Empowr PS Total Knee replacement, while chiseling for bone removal in the box area, femoral chipping has occurred in surgery.
BD is conducting a voluntary product recall of the BD Spinal Anesthesia Tray, Cat (Ref) 405671, lot B01K089D since a very low number of trays are incorrectly labeled as BD Single Shot…
Edits to Particle field definition parameters may not be saved when the field definition window is saved.
The firm sent the Technical Bulletin to consignees who received the reliability updated neoBLUE blanket LED Phototherapy Systems between March 2016 to August 2016. The reliability update to…
Package Defect: Products may be at risk for having a slit defect on the package and that may affect the product sterility.
Package Defect: Products may be at risk for having a slit defect on the package and that may affect the product sterility.
Defects: Product may be discolored and brittle resulting in the inability of the user to don the gloves without tearing.
The firm was notified by their supplier that the products may be contaminated with Listeria monocytogenes..
The firm was notified by their supplier that the products may be contaminated with Listeria monocytogenes..
Farmer's Market Buffalo Hot Peanuts contained undeclared cashews and wheat. Labeling error at manufacturer found Farmer's Market Trail Mix labeled as Farmer's Market Buffalo Hot Peanuts.
Customer reported a small piece of rubber inside one variety of the recalled product.
The product has been recalled because it has the potential to be contaminated with Listeria monocytogenes.
Milk Chocolate covered pretzels have incorrect rear label. The rear label is for the Dark Chocolate pretzels which lack allergen declaration.
Produces contains undeclared milk.
Products contain an excessive amount of TBHQ (tert-Butylhydroquinone) and DMPS (dimethyl polysiloxane).
Browse recent months with enough recall history for useful comparison.
