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Class Ii Recall

All articles tagged with #class ii recall

health13 days ago•78 min saved

FDA Recalls 13,500 Chlorthalidone Bottles Over Dissolution Failures

The FDA has issued a Class II recall for 13,567 bottles of chlorthalidone 25mg tablets manufactured by Inventia Healthcare Limited. The recall, initially issued on September 3 and upgraded on September 17, stems from the medication failing dissolution specifications, which may prevent the drug from releasing its active ingredient properly. This is the second recall for this specific medication in three months, following a similar issue with Rising Pharma Holdings in June. Chlorthalidone is a diuretic used to treat high blood pressure and fluid retention. Patients are advised to stop using the affected product and consult their healthcare provider for an alternative.

via AOL.com|

#chlorthalidone #class-ii-recall #dissolution-specifications

health23 days ago•404 min saved

Six Intercon Hand Soaps Recalled Across 15 States for Possible Bacterial Contamination

Intercon Chemical Co. voluntarily recalled six hand soap products (2,696 cases) due to potential contamination with bacteria including Pseudomonas and Serratia species. The recall covers 15 states (California, Georgia, Illinois, Iowa, Maryland, Mississippi, Nebraska, New York, North Carolina, North Dakota, Pennsylvania, South Carolina, Texas, Washington, Wisconsin) and was escalated by the FDA to Class II on Sept. 11. Consumers should stop using the recalled products and monitor for symptoms; refunds have not been announced. If illness occurs after use, seek medical attention.

via NBC News|

#bacteria-contamination #class-ii-recall #hand-soap

health2 months ago•3 min saved

Nationwide Recall: Subpotent Levothyroxine Pills Prompt FDA Action

The FDA issued a Class II recall for certain levothyroxine sodium tablets used to treat hypothyroidism after tests found subpotent levels of the active ingredient, potentially reducing effectiveness. Major Pharmaceuticals and Cardinal Health distributed twelve recalled dosages nationwide in cartons; the recall covered multiple lots, but the total quantity was not disclosed.

via NBC 7 San Diego|

#class-ii-recall #fda-recall #health

science2 months ago•45 min saved

FDA recalls about 244,432 carbamide peroxide ear drops nationwide for subpotent ingredient

The FDA is recalling about 244,432 containers of 6.5% carbamide peroxide earwax-removal products distributed nationwide due to subpotent active ingredient, potentially yielding ineffective results. The recall, classified as Class II, covers multiple brands (including CVS Health, Clinere, QC Quality Choice, TopCare Health, Audiologist's Choice, Family Wellness, Good Neighbor Pharmacy, Leader, Foster & Thrive, Meijer, CAREone) and advises consumers not to use these lots until replacement or further guidance is issued.

via Yahoo|

#carbamide-peroxide #class-ii-recall #earwax-removal

health7 months ago•1 min saved

Blue-plastic contamination prompts nationwide peanut butter recall

The FDA issued a recall for three Ventura Foods-produced peanut butter products after detecting blue plastic foreign material, affecting jars sold across 40 states. The recall was reclassified to Class II on Feb 12, 2026. There is no FDA-mandated remedy, but customers can obtain refunds by returning recalled jars to the place of purchase; a full list of affected items is in the recall report.

via WKRC|

#class-ii-recall #fda-recall #foreign-material

health1 year ago•2 min saved

FDA Recalls Over 20,000 7Up Cans for Sugar Labeling Errors

The FDA has recalled nearly 2,000 cases of 7Up Zero Sugar Tropical Soda due to a labeling error that caused full-sugar soda to be sold as zero sugar, posing health risks especially for diabetics and those managing sugar intake. The recall affects products with specific UPCs and lot numbers, and consumers are advised to check their cans and return any affected products for a refund.

via The Times of India|

#7up-zero-sugar-tropical-soda #class-ii-recall #fda-recall