Dakin's Solution recall: CGMP Deviations
Dakin's Solution, a) sodium hypochlorite 0.125%, quarter strength, NDC 0436-0672-16, b) sodium hypochlorite 0.25%, half strength, NDC 0436-0936-16, c)…
Why was Dakin's Solution recalled?
CGMP Deviations: products were stored outside the drug label specifications.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and identifiers are part of this recall.
- Product
- Dakin's Solution, a) sodium hypochlorite 0.125%, quarter strength, NDC 0436-0672-16, b) sodium hypochlorite 0.25%, half strength, NDC 0436-0936-16, c)…
- Recalling firm
- Mckesson Medical-Surgical Inc. Corporate Office
- Quantity
- 113 bottles
- Distribution
- Nationwide in the USA.
- Recall date
- August 17, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)