MAGNOLIA VEGETABLE PROCESSORS recalls Wickles Relish 16oz glass jars - 6 jars per case (Class III)
Wrong Label applied to Product.
Newest first, across both agencies. FDA covers most food; USDA FSIS covers meat, poultry and egg products, and the two share no identifiers — so this list is the only place they sit together.
Wrong Label applied to Product.
Specific lot of Organic Steel Cut Oats, may actually contain Organic Beet Sugar
Vitamin D dietary supplement may contain Coq10
Possible plastic within final product packaging.
Soy Lecithin listed in ingredients statement but soy is not mentioned in the contains statement.
CGMP Deviations: Presence of damaged tablets
Cup label identifies product as Peaches, product inside cup, and label on lid is Mixed Fruit
Foreign capsules included in bottle. Undeclared ingredients.
Failure to manufacture product in accordance with 21CFR part 114: Acidified Foods
cGMP Deviation: Presence of damaged tablets
Firm determined that pesticide Bifenazate MRL is out of compliance for the US market. US MRL = 5ppm. Product tested = 5.8ppm.
Incorrect active ingredient is listed on product label
Elevated water activity level in shelf-stable products.
Fish decomposition.
One lot of uncooked shrimp was inadvertently packaged as cooked shrimp.
Vitamin D3 stability sample analyzed and found to be less than 100% of label claim.
Product contains undeclared FD&C Red No. 40.
Undeclared Red #40
Undeclared ingredients on retail packaging, including but not limited to certified colors Red #40 and Blue #1
Pasteurized donor human milk may contain trace amounts of dextromethorphan.
Incorrect labeling on bottom of packaging (undeclared peanuts).
The firm received a consumer complaints that the product was spoiled.
Product may have low levels of imidacloprid in excess of the tolerance of 0.05 ppm.
Rancidity and packaging integrity defects in GF sprouted rolled oats
An internal quality review found that an ingredient contained a milk derivative, but milk was not declared on the label.
Product may contain nightshade
CCP deviation with the wash process
CCP deviation associated with wash process, portion of affected product left company control.
Product utilized a gluten-free claim but has as an ingredient a fermented soy sauce that is produced from wheat which was not processed to remove the gluten prior to fermentation.
Stabilizer was made with Citric Acid instead of Sodium Citrate.
Undeclared black bean powder, jalapeno pepper powder, paprika, extract of paprika and disodium inosinate and disodium guanylate.
Tortilla chips turn stale prior to expiration date.
CGMP Deviations: Presence of damaged tablets
Sample analysis revealed product is sub-potent for Vitamin D
Water filled bottles labeled as Similac Pro-Advance.
Critical Control Point (CCP) deviation associated with wash process, low levels of chlorine wash, affected product was sent to distribution chain.
FDA sample analysis of Biotin 1000mg Lot #1345 showed the product Biotin content to be 0.8% of label claim.
Product contains dried peaches, but front labeling of product stated dried plums
Due to different color of powder in capsules. Firm's evaluation determined product low potency.
FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.
Customer reports of label error. Front panel states strength of 1000 mg although supplement fact is correct in stating 1000 mcg.
Undeclared sulfites in product label.
The allergen peanut is included on the label, but missing from the ingredient statement.
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Notified by supplier that flax seed used in products is under recall due to detection of unapproved herbicide.
Potentially contaminated with an unapproved herbicide, haloxyfop.
Firm received customer inquiry of why wheat is listed in the ingredient list of a product that is "Gluten Free".
Products contain undeclared soy protein isolate.
An ingredient used in the manufacture of finished product was discovered to have been grown using unapproved herbicide.
In House testing found a residue of 0.927 ppm of Zeta-cypermethrin on raspberries, which is above the U.S. MRL of 0.800 ppm
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