Could cause temporary or reversible harm; serious harm is unlikely.
Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commingled in a bottle of Extra Strength Acetaminophen 500 mg contents 1000 count bottle.
| Brand name | ACETAMINOPHEN |
| Generic name | ACETAMINOPHEN |
| Active ingredient(s) | ACETAMINOPHEN |
| Distributed by / for | Major Pharmaceuticals 17177 N. Laurel Park Drive, Suite 233 Livonia, MI 45162 USA |
| NDC | 0904-6730-60 |
| Full product label | Major Extra Strength Acetaminophen Tablets, 500 mg Pain Reliever/Fever Reducer, packaged in a) 100-count bottles (NDC 0904-6730-60; UPC 3 09046 73060 6) and b) 1000-count bottles (NDC 0904-6730-80; UPC 3 09046 73080 4) Distributed by Major Pharmaceuticals 17177 N. Laurel Park Drive, Suite 233 Livonia, MI 45162 USA |
| Recalling firm | Contract Pharmacal Corporation |
| Distribution | Nationwide within the United States |
| Quantity | a) 1176 bottles b) 6,216 bottles |
| Recall initiated | 2020-02-03 |
| Report date | 2020-02-19 |
| Recall completed | 2024-04-22 |
| Recall number | D-0858-2020 |
| Classification | Class II |
| FDA status | Terminated |
| Origin on file | Hauppauge NY United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗