Every recall we track for Viatris, Inc. — 23 in all — plus the complaints and injury reports the public filed about them.
Viatris recalls 3mg Xanax XR tablets with failed dissolution specs. This may affect medication effectiveness. Contact Viatris for details.
Viatris recalls Cardura XL 4mg extended-release tablets due to impurity issues found during stability testing. This affects specific lot numbers and requires patient consultation with healthcare providers.
Viatris recalls Cardura XL 8mg extended-release tablets due to impurity issues detected in stability testing. Affected lots may pose risks if stored improperly.
Viatris recalls Levothyroxine Sodium Tablets (88 mcg) with potency failures. These tablets may not provide correct hormone levels, risking health issues. Check NDC codes and expiration dates for affected batches.
Viatris recalls Levothyroxine Sodium Tablets (137 mcg) due to potency failures. Affected lots expire Dec 2024-March 2025. Check NDC codes 0378-1823-77 and 0378-1823-10 for affected products.
Viatris recalls 90-count and 1000-count Levothyroxine Sodium Tablets USP 175 mcg due to potency failures. These tablets may not provide correct thyroid hormone levels, risking health issues.
Viatris recalls 90-count and 1000-count Levothyroxine Sodium Tablets (112 mcg) due to potency failures. Affected lots expire Feb 2025 or later. Contact for return instructions.
Viatris recalls 90-count and 1000-count Levothyroxine Sodium Tablets (200 mcg) due to potential potency failures. These tablets may not deliver the correct dosage, risking treatment effectiveness.
Viatris recalls 50 mcg levothyroxine tablets with potency failures. These tablets may not provide correct thyroid hormone levels. Affected lots expire April 2025 or later.
Viatris recalls 150 mcg levothyroxine tablets with potency failures. Affected lots expire June 2025. Stop using if you have these specific NDC numbers.
Viatris recalls Cardura XL 4mg tablets (NDC 0049-2040-10) made in Singapore with potential impurities. Stop using if you have these specific lots.
Viatris recalls Cardura XL 8mg tablets made in Singapore with potential impurities. This recall affects specific lots of the prescription medication. Consumers should contact the manufacturer for details.
Viatris recalls 500mg Valacyclovir tablets with possible missing 'M 122' imprint. This may affect identification and safety for prescription use.
Viatris recalls Levsin injection (0.5 mg/ml) due to quality program discontinuation. This may affect product identity, strength, quality, and purity. Check NDC #0037-9001-05 and lot 101241A.
Viatris recalls 10x1mL Octreotide syringes due to glass particles. Stop using if you have these syringes before expiration.
Viatris recalls Ampicillin injections due to a single strand of hair found in one vial. This may cause allergic reactions. Stop using affected lots immediately.
Viatris recalls 3mg Xanax XR tablets with failed dissolution specs. This may affect medication effectiveness. Check NDC 0009-0068-07 and lot DX7983 for affected products.
Viat: Viatris recalls 3mg alprazolam XR tablets due to failed dissolution testing. This may affect medication effectiveness. Check NDC 59762-0068-1 and lot # EH834: 07977, exp. August 2023.
