
FDA•LOW
Fexofenadine Hydrochloride Tablets 180 mg
Ohm Laboratories is recalling 180 mg Fexofenadine Hydrochloride tablets due to failed impurities and degradation specifications.

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.

Sandoz is recalling Focalin XR 5 mg capsules due to missing or incorrect lot numbers and expiration dates on the product labels.

Amneal Pharmaceuticals is recalling Primidone 50 mg tablets due to potential cross-contamination with Acemetacin API.

Fresenius Kabi is recalling Epinephrine Injection 1mg/mL vials due to out-of-specification stability test results.

Sato Pharmaceutical is recalling Yunker Energy & Health Herbal Supplement due to a failure to meet label claims for Vitamin E content.

Eugia US LLC is recalling Lidocaine HCl Injection 2% because the label wrap covers the barcode, making it difficult to scan.

AbbVie is recalling 10 mL bottles of Pred Mild ophthalmic suspension due to failed stability specifications.

Aveva is recalling 14 mg Nicotine Transdermal System Patches due to elevated levels of oxidative-related impurities.

American Health Packaging recalls Primidone 250 mg tablets over API cross contamination.
2 products
Sagent Pharmaceuticals is recalling Busulfan Injection (NDC 25021-241-10) due to failed impurities and degradation specifications.

Golden State Medical Supply is recalling Primidone Tablets 50 mg due to cross-contamination with trace amounts of Acemetacin API.
2 products
Lannett Company is recalling Primidone 250mg Tablets (NDC 0527-1231-01) due to potential cross-contamination with Acemetacin API.

Unichem is recalling 5 mg buspirone hydrochloride tablets due to subpotency, which may reduce the medication's effectiveness.

Tops Markets recalls Garland Fresh and Christopher Ranch Peeled Garlic 6 oz. bags over botulism risk from temperature abuse.
2 products
CVS is recalling Lidocaine Wound Gel (NDC 59898-950, 0.5 oz) due to failed pH specifications.
