SunOpta Grains and Foods Good & Gather Mixed Fruit Blend Pineapple Chunks, Sliced recall — FDA F-1269-2023
Fruit products have the potential to be contaminated with Listeria monocytogenes.
Complete FDA and NHTSA recall records dated in July 2023.
These records include useful source details for the selected month.
Fruit products have the potential to be contaminated with Listeria monocytogenes.
Fruit products have the potential to be contaminated with Listeria monocytogenes.
Fruit products have the potential to be contaminated with Listeria monocytogenes.
Undeclared milk and egg
The product labels include a Contains statement that did not disclose sesame for the product that contains sesame. Sesame is included Ingredient statement.
Fruit products have the potential to be contaminated with Listeria monocytogenes.
CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Superpotent Drug: Out of Specification (OOS) results observed for unit dose content.
CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.
Lack of Assurance of Sterility
Labeling: Label Error on Declared Strength: some cartons labeled and containing 20 mg may have an external label placed on the side of the carton indicating strength as 10 mg.
Lack of Assurance of Sterility
CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.
CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.
Lack of Assurance of Sterility
Ford Motor Company (Ford) is recalling certain 2023 Escape, Super Duty F-250, Super Duty F-350, Super Duty F-450, and Super Duty F-550 vehicles equipped with a digital instrument panel…
Ford Motor Company (Ford) is recalling certain 2021-2023 F-150 vehicles equipped with a single exhaust system. Contact with the rear axle housing may damage the wiring harness, causing the…
Affected product lots were mislabeled as "STERILE PVP SLN" when they should have been titled "NON-STERILE PVP SOLUTION, STERILE PACKAGING".
Specific diluent lot numbers showed that conductivity, osmolality, and pH were out of manufacturing specifications.
There is an overall reported incidence rate of 0.77% related to observed or potential air embolism during procedures in which the ASDS product was used.
There is the potential for out of specification device geometries. widths, lengths, heights, and lordotic angles to accommodate patient anatomy. These devices can be inserted between two…
Potential to cause biased results in the upper end of the reportable range for the quantitative measurement of Transferrin, C3, C4, IgA, IgG and IgM. Within the reference interval, the…
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.