
FDA•LOW
Povidone Iodine/Proparacaine Ophthalmic Solution
Imprimis NJOF recalls ophthalmic solution for being subpotent, risking reduced efficacy.

Imprimis NJOF recalls ophthalmic solution for being subpotent, risking reduced efficacy.

Ajanta Pharma recalls Fluphenazine HCl 1mg tablets (NDC 27241-255-01) due to impurity out-of-specification.

Trokendi XR (topiramate) 50 mg capsules recalled over failed dissolution specs.

Wonton Specialist recalls noodles and dumpling skins for undeclared FD&C Red No. 40, an allergen risk.
6 products
New York Blood Center recalls apheresis red blood cells over incorrect anticoagulant ratio.

Bionpharma recalls Doxylamine Succinate and Pyridoxine HCl 10 mg/10 mg tablets over foreign tablets or capsules.

Africando Alfredo Hot Sauce recalled for undeclared wheat and soy allergens.

Safecor recalls Ibuprofen oral suspension syringes over cross-contamination risk.

Paragon 28 recalls Navicular Cage foot implant (Model 6123S R) due to elevated oxygen levels.
2 products
Honeyville Yellow Color 1-gal recalled for undeclared Red #40 allergen.

Kanni Delight Fresh Frozen Vannamei White Shrimp recalled over nitrofurans detected in the product.

Central Admixture recalls pediatric TPN bags due to incorrect formulation.

Red Cross recalls Apheresis Platelets, PAS, Leukocytes Reduced, Pathogen Reduced units lacking required yield testing.

Siemens recalls Syva Emit Tox Tricyclic Antidepressant Calibrator/Controls due to out-of-specification sodium azide concentration.

Siemens recalls Syva Emit Disopyramide Assay due to out-of-spec sodium azide concentration; risk of mild irritation.

Ascend recalls Dabigatran Etexilate 75mg/150mg capsules over impurity spec failures.
6 products
Island Pacific and Nautilus imitation crab sticks and flakes recalled for undeclared STTP.
6 products
Lidolog Kit is being recalled because the label wrap obscures the barcode, making it difficult to scan.
2 products
Supernus recalls Trokendi XR 25mg capsules over failed dissolution specs.
3 products
Ascend recalls Dabigatran etexilate capsules (110 mg, 150 mg) over impurity test failures.
2 products
Ohm Laboratories is recalling 180 mg Fexofenadine Hydrochloride tablets due to failed impurities and degradation specifications.

ANI Pharmaceuticals is recalling Hydroxyzine Hydrochloride Oral Solution, 10 mg/5 mL, due to the presence of a foreign substance.

Lunch Box Kitchen Turkey & Cheddar Sub recall: mislabeled (may be roast beef & Swiss); BEST BY 06/14/26.

United Salt Corp recalls mislabeled salt: plain vs. iodized mix-up.
