Hi-Tech Pharmacal Co., Inc.: food safety notices
Notices that name Hi-Tech Pharmacal Co., Inc. as producer, shipper or recalling firm.
Notices3since 28 Jul 2014
Latest23 Dec 2014United States
CountryUnited States
Notices
| Date | Source | Origin | Product | Hazard | Type |
|---|---|---|---|---|---|
| 23 Dec 2014 | US | United States | FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059, NDC 50383-778-05 --- HI-TECH PHARMA Hi-Tech Pharmacal Co., Inc. | Other | Recall · Class II |
| 25 Aug 2014 | US | United States | Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACA Hi-Tech Pharmacal Co., Inc. | Documents and labelling | Recall · Class III |
| 28 Jul 2014 | US | United States | Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACA Hi-Tech Pharmacal Co., Inc. | Composition (nutrients and actives) | Recall · Class III |
Firm names are reproduced as each authority publishes them. A notice concerns specific lots or consignments and is not a finding about the company as a whole.