Skip to content
Food Recall Radar
Class IIFDAF-1018-2023

Amin Trading Agency LLC recalls Maggi Masala ae Magic, 6 grams, Packaged in plastic sachets. 1920 sachets per case. (Class II)

Amin Trading Agency LLC recalled Maggi Masala ae Magic and Everest Sambhar and Garam Masala spice products due to potential Salmonella contamination. Consumers who use these spices risk serious foodborne illness.

Class IIEating this product may cause temporary or medically reversible health problems; serious harm is unlikely.

Product

Maggi Masala ae Magic, 6 grams, Packaged in plastic sachets. 1920 sachets per case.; Everest Sambhar Masala, 100 grams, Packaged in paper cartons. 120 cartons per case; Everest Garam Masala, 100 grams, Packaged in paper cartons. 120 cartons per case

  • Maggi Masala ae Magic, 6 grams, Packaged in plastic sachets. 1920 sachets per case.
  • Everest Sambhar Masala, 100 grams, Packaged in paper cartons. 120 cartons per case
  • Everest Garam Masala, 100 grams, Packaged in paper cartons. 120 cartons per case

Reason for recall

Product may be contaminated with Salmonella

Affected products (3)

Recall #ProductLot / codeStatus
F-1018-2023Maggi Masala ae Magic, 6 grams, Packaged in plastic sachets. 1920 sachets per case.20640 455AATerminated
F-1019-2023Everest Sambhar Masala, 100 grams, Packaged in paper cartons. 120 cartons per caseU04D384296Terminated
F-1020-2023Everest Garam Masala, 100 grams, Packaged in paper cartons. 120 cartons per caseU25D390373Terminated

Related recalls

Likely Class I(our estimate, pending agency classification)FDA

Made Fresh Salads Inc. recalls Made Fresh Salads Ready to Eat Deli Style Salads and cream cheese

Made Fresh Salads recalled ready-to-eat deli style salads and cream cheese due to potential Listeria monocytogenes contamination. Listeria infection can cause severe illness and is particularly dangerous for pregnant women, young children, and immunocompromised individuals.

Foreign materialListeriaBrand: Made Fresh Salads, Northside
Likely Class II(our estimate, pending agency classification)FDA

American Regent, Inc. recalls American Regent Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

American Regent recalled Epinephrine Injection USP 30 mg/30 mL multi-dose vials due to potential particulate matter and loss of sterility assurance. Users of affected vials face serious risk if the contamination is present, as injection of particles or non-sterile product could cause infection or other harm.

Foreign materialBrand: American Regent

Do not rely on this site to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Always check the original FDA or USDA notice, linked on every recall page.