Merck & Co Inc: 5 recalls on record

Recalls filed with 1 agency: FDA (5).

First recall on record: May 14, 2014. Most recent: August 20, 2025.

Risk classification: Class II: 1 · Class III: 4

Most recent recalls

DateAgencyProduct
August 20, 2025FDABelsomra (suvorexant) tablets, 10mg, 30 Tablets in 3 Blister Cards per Carton, Each Blist…D-0584-2025
May 14, 2014FDALiptruzet (ezetimibe and atorvastin) tablets,10 mg/80 mg, a) 30 count blister (NDC 665…D-1312-2014
May 14, 2014FDALiptruzet (ezetimibe and atorvastin) tablets,10 mg/20 mg, a) 30 count blister (NDC 665…D-1310-2014
May 14, 2014FDALiptruzet (ezetimibe and atorvastin) tablets,10 mg/40 mg, a) 30 count blister (NDC 665…D-1311-2014
May 14, 2014FDALiptruzet (ezetimibe and atorvastin) tablets,10 mg/10 mg, a) 30 count blister (NDC 665…D-1309-2014

Questions about this company

How many recalls does Merck & Co Inc have?
Recalert has 5 U.S. recalls on record for Merck & Co Inc, published between May 14, 2014 and August 20, 2025.
What was the most recent Merck & Co Inc recall?
FDA recall D-0584-2025, published August 20, 2025: Belsomra (suvorexant) tablets, 10mg, 30 Tablets in 3 Blister Cards per Carton, Each Blister Card contains 10 Tablets, Rx only, Merck Sharp & Dohme LLC, Rahway, NJ 07065, USA, NDC 0006-0033-10 (Shellp…
Which agencies have handled Merck & Co Inc recalls?
Merck & Co Inc appears as the recalling firm in recalls from: FDA (5).

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