Alaska recalls

Product is potentially under-processed.

Salmonella spp. identified in finished product testing

Failed Impurities/Degradation Specifications: out of specification at the time of testing i.e. 20th month stability testing.

FOR IMMEDIATE RELEASE – Date – Ferndale, Michigan. Nalpac is voluntarily recalling DTF Sexual Chocolate it purchased and resold. The products have been found to contain sildenafil and tadalafil.

Liquid Blenz Corp of Rockville Center, NY is recalling all codes of Good Brain Tonic because of Botulism potential. Botulism is a potentially fatal form of food poisoning and can cause the following symptoms: general weakness, dizziness, double-vision, and trouble with speaking or swallowing. Diffic

Product Contamination

The FDA has issued an Advisory without batch numbers or expiration dates. At the request of the FDA, RAW FARM is issuing a Voluntary Recall of the batches of cheese below and any batches produced prior to these dates.

Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient statement and allergen information do not include wheat or soy.

Metal fragments. The potential foreign object is a hard, metal (stainless steel), curled spring. Dimensions of a similar spring measure 2.27mm in cross-sectional thickness and 25.38mm in coil width. Spring ends are not sharp but may be sharp if broken/ cut.

Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.

Foreign object (glass) found inside sealed container of finished product.

Foreign object (glass) found inside sealed container of finished product.

FOR IMMEDIATE RELEASE – 03/30/2026 - Flushing, New York, Aphreseller (Ebay seller ID), Buy-herbal.com is recalling all lots of Kian Pee Wan capsules to the consumer level. FDA analysis has found that the product contains the undeclared drug ingredients dexamethasone and cyproheptadine. Products cont

Produced Without Benefit of Inspection

Undeclared allergen ingredients (sesame and wheat) in Zaatar Spice mix.

A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.

Bridgewater, New Jersey, Amneal Pharmaceuticals LLC is voluntarily recalling one lot of Magnesium Sulfate in Water for Injection, USP, 4g/100mL, IV bag, to the hospital level. A Magnesium Sulfate in Water for Injection pouch was found to contain an IV bag of Tranexamic Acid in 0.7% Sodium Chloride I

Product may be contaminated with Salmonella

Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.

Product Contamination

Unreported Allergens

Potential to be contaminated with Salmonella

Product Contamination

Product Contamination

Foreign material (small hard plastic fragments).

Foreign material (small hard plastic fragments).

Undeclared Milk Allergen

Undeclared Milk Allergen

Undeclared Milk Allergen

potential Clostridium botulinum contamination