BrightFarms Baby Kale (3 oz. package)
CHI Greenhouse
Bright Farms Inc. dba CHI Greenhouse LLC is initiating a voluntary recall of packaged produce due to the potential presence of E. coli.
95,075 total recalls in our database
CHI Greenhouse
Bright Farms Inc. dba CHI Greenhouse LLC is initiating a voluntary recall of packaged produce due to the potential presence of E. coli.
CFS West Holdings
Products potentially contain undeclared egg.
Meijer Distribution
Meijer Inc. is voluntarily recalling multiple processed vegetable products following a supplier's recall due to potential contamination with Listeria monocytogenes.
CHI Greenhouse
Bright Farms Inc. dba CHI Greenhouse LLC is initiating a voluntary recall of packaged produce due to the potential presence of E. coli.
Meijer Inc. is voluntarily recalling multiple processed vegetable products following a supplier's recall due to potential contamination with Listeria monocytogenes.
Amneal Pharmaceuticals
Presence of Particulate Matter
cGMP Deviations: lack of quality assurance at the API manufacturer.
Failed Impurities/Degradation Specifications.
Labeling: Incorrect or Missing Package Insert.
Allergan Sales
Failed Impurities/Degradation Specifications.
Amerisource Health Services
Failed Stability Specifications
Jubilant Cadista Pharmaceuticals
Marketed without an approved NDA/ANDA: Bottles were released prior to final approval.
Superpotent drug: out of specification result for potency
Superpotent Drug: Subpotent Drug. FDA analysis found this product to be Out of Specification for assay which could result in either Subpotent and/or Superpotent tablets.
There have been reported incidents of fluid leaks at the luer connection. Leaks have been confirmed to originate from, or near, the reservoirs clearcolored female luer connecter.
Arthrex part number AR-501-UFLC, size 3, batch 10123297, has the incorrect part number AR-501 ΒΏUFRA, size 1 printed on the patient label inside the box.
Observed instability of the device.
The Broad Quantification option of the Symbia product software version VB20A may not allow modification of two data input values. The failure occurs when the system with the Broad Quantification option is calibrated with phantoms that do not have a volume of 6500ml and/or when residual dose needs to be entered.
An undetected shift between the information displayed in the navigation software and the actual patient anatomy
Smith & Nephew
A single lot of INTERTAN 10S 10 MM X 18 CM 130 D was manufactured with the screw inserted upside down.