Class II recall
Coverage of Class II recall in the Nexus archive.
- Rohto is recalling nearly 12 million eye drop bottles over sterility concerns
Rohto is recalling nearly 12 million eye drop bottles due to sterility concerns. The FDA classified the recall as Class II, indicating the products may cause temporary effects but are unlikely to result in serious harm.
- Recall alert: 11M cartons of Rohto Cooling Eye Drops recalled
The FDA classified a recall of over 11 million cartons of Rohto Cooling Eye Drops as a Class II recall due to potential sterility issues. The recall, initiated by Rohto-Mentholatum (Vietnam-based company), affects multiple variants of the eye drops, with the FDA noting temporary or reversible health risks if used.
- Recall alert: Thyroid medication Levothyroxine recalled nationwide
The FDA has classified a nationwide recall of Levothyroxine, a thyroid medication, as a Class II recall due to being 'subpotent.' Major Pharmaceuticals, based in Dublin, Ohio, issued the voluntary recall on July 13, with the FDA officially marking it Class II on July 17.
- Amy’s Kitchen recalls more than 180K cans of soup due to ‘potential for spoilage’
Amy’s Kitchen is recalling 184,200 cans of Amy’s Organics Lentil – Light in Sodium soup due to a canning defect causing potential spoilage. The FDA classified the recall as Class II, indicating temporary health risks, and affected products can be identified by lot number 60D0924 and best-by date April 2027.
- Amy’s Kitchen recalls more than 180K cans of soup due to ‘potential for spoilage’
Amy’s Kitchen is recalling over 184,000 cans of its lentil soup due to a manufacturer defect in the can’s easy-open tab, which could lead to spoilage. The FDA classified the recall as Class II, indicating potential for temporary health issues, and the affected product was sold in 28 U.S. states and Canada.
- Recall alert: 184K cans of Amy’s Organic Soups recalled for potential spoilage
Amy’s Kitchen Inc. recalled 184,000 cans of lentil soup due to potential spoilage. The FDA classified the recall as Class II, indicating low risk of serious health issues.
- Recall alert: 11K bottles of blood pressure medication recalled
The FDA recalled 11,460 bottles of 25mg chlorthalidone tablets due to failing dissolution specifications, distributed by Rising Pharma Holdings. The Class II recall indicates potential temporary adverse health effects.