Wonton Specialist Inc recall — FDA H-1321-2026
Undeclared FD&C Red No. 40
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Undeclared FD&C Red No. 40
Product tested positive for undeclared milk allergen.
Sesame is not declared in the ingredient statement but is declared in the statement of identity.
Milk is not declared in the Contains statement.
Product may be contaminated with Salmonella.
Foreign object: metal fragments
Product tested positive for undeclared milk.
Sesame is not declared in the ingredient statement but is declared in the statement of identity.
Product has high patulin levels
Foreign object: metal fragments
Sesame is not declared in the ingredient statement but is declared in the statement of identity.
Ford Motor Company (Ford) is recalling certain 2026 F-150 vehicles.The stabilizer rod fasteners may not have been tightened properly during manufacturing, which can allow the rod to shift…
Ford Motor Company (Ford) is recalling certain 2026 F-150 vehicles. Incorrect rear axle tail bearings may have been installed, which can result in rear wheel lock-up or driveshaft…
Ford Motor Company (Ford) is recalling certain 2023-2027 F-150 vehicles. The fuel tank may be improperly secured and leak fuel, or detach from the vehicle while driving.
Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list
Product has the potential to be spoiled.
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2024 Toyota Tacoma Hybrid, 2025 Tundra Hybrid, Tundra, 2026 RAV4 Hybrid, 4Runner i-Force Max Hybrid, and 4Runner…
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples…
Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not…
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples…
Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.
Kits contain a potentially contaminated component which were recalled by the manufacturer
Test manufactured with an expired ingredient which may present as either a false negative or positive.
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