Vadilal Quick Treat Custard Apple Pulp Net Wt, 1kg/35.27-oz. Product code FPEP44302 UPC:8901777282168 Best Before September 2023
Vadilal Industries USA
Product may be contaminated with Salmonella
95,025 total recalls in our database
Vadilal Industries USA
Product may be contaminated with Salmonella
Whole Foods Market Brand 365
Undeclared egg
Pecans although listed in the Ingredient Statement, was omitted from the CONTAINS statement.
Dollar Tree Distribution
Potential exposure to rodents and rodent activity in the distribution center.
Preferred Pharmaceuticals
CGMP deviations
cGmp Deviations
Labeling: Label Mix-Up-The primary label on the front of the bottles have 50% Isopropyl Alcohol affixed to the containers. However, the product inside the bottle is Hydrogen Peroxide, Topical Solution USP with active ingredient Hydrogen Peroxide (stabilized) 3%, 32 FL Ounces. The back label is correct. Product is packaged in dark bottles.
Failed impurities/degradation specifications
Labeling - product contains undeclared ethyl alcohol
cGMP deviations
Dollar Tree Distribution
CGMP Deviations: Potential exposure to rodents and rodent activity in the distribution center.
Labeling - product contains undeclared ethyl alcohol
Morton Grove Pharmaceuticals
Failed Impurities/Degradation Specifications: higher than permissible levels of unknown impurities were found in the drug product.
There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
Microbiologics
This strain should be resistant to high levels of Gentamicin and be resistant to Gentamicin Synergy. A specific lot was found susceptible to Gentamicin Synergy during in-house testing.
There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
Real-time shelf life testing failed at 24 months
Stryker received two (2) complaints for units from specific lots of Inner and Outer Dilators not fitting together properly during a surgical procedure. Some dilators from these lots and from other lots were subsequently determined to be affected by a manufacturing nonconformance.
Respironics California
A limited number of ventilators were assembled with expired adhesive. If the adhesive fails, a bracket may become loose and potentially damage the capacitors, which could cause the ventilator to stop providing ventilation to the patient. This failure may either activate both visual and audible alarms, or it may not sound or display an alarm (a silent shutdown).
Acorn Stairlifts
The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use.