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.
Failed Impurities/Degradation Specifications: Out of Specification for an unknown impurity was observed during the 18 month stability testing.
The device may exhibit premature battery depletion.
The device may exhibit premature battery depletion.
There is a potential to generate falsely-depressed patient results in the cuvettes adjacent to the detached segment post for any assay run on the c4000 instrument.
During internal cycle testing of A-Series lifts Handicare has found that the A-Series lift strap for lifts manufactured between April 25, 2017 and June 12, 2017 may wear prematurely at max…
A limited amount of Carina mobile lifts have been delivered with a too small locking pin. If a locking pin smaller than the correct size is mounted on the Carina mobile lift, the locking…
Equipment malfunction resulted in the inclusion of very small metallic fragments and particulate matter in some lots of salt tablets.
Royal Asia brand Shrimp Wonton Noodle Soup is recalled due to undeclared egg.
Silver Spring is recalling Waterfront Bistro Tartar Sauce because an incorrect back label does not identify egg.
Product has the potential to be contaminated with Listeria monocytogenes.
Milk Chocolate Tasty Treats nonpareils have undeclared milk as the ingredient statement on the package is incorrect.
The firm was notified that an ingredient used to manufacture the recalled product may contain wood slivers.
Fuji apples are recalled because Thiabendazole was detected at 6.9 ppm.
Failed impurities/degradation specifications: Famotodine has an out of specification result for an individual related substance observed during routine stability testing of a batch for…
CGMP Deviations; FDA analysis deterrmined that the product does not contain glutamine and two unknown impurities were observed
Labeling: Incorrect or missing package insert. One lot of Mobic Tablets is packaged with an incorrect insert.
There is a potential failure of the top plate assembly, which is the component that connects the seating system of the wheelchair to the base.
The hot stamp label on the bag incorrectly states the material of the vinyl (bag) container. The bags are correctly made with PVC material, as ordered and as labeled on the inner and outer…
The high control for the kit is recovering low and may be out of range for assigned values.
Radiometer has recently become aware that a few of the AUTOCHECK 5+ level 2 ampoules, will give incorrect results for pCO2 and pO2. A defective QC ampoule will for: " pCO2 give a result…
Potential for intermittent lighting (flickering) during use.
There is a potential failure of the top plate assembly, which is the component that connects the seating system of the wheelchair to the base.
The device had an incorrect printed calibration value on the calibration certificate.
The dowel pins (P/N 16082) that fit in the left and right leg pivot castings (P/Ns 16049/16056) can rotate and gradually maneuver out of the leg casting after several hundred deployment and…
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