FDA Drug Recalls

Recalls / Class II

Class IID-1323-2022

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) sodium hypochlorite 0.5% full strength, NDC 0436-0946-16, Antimicrobial, 473 mL (16 fl oz) bottle, Century Pharmaceuticals, Inc.

Brand names
Dakins Quarter, Dakins Half, Dakins Full
Generic name
Sodium Hypochlorite
Active ingredient
Sodium Hypochlorite
Route
Topical
NDCs
0436-0672, 0436-0936, 0436-0946

Why it was recalled

CGMP Deviations: products were stored outside the drug label specifications.

Recalling firm

Firm
Mckesson Medical-Surgical Inc. Corporate Office
Manufacturer
Century Pharmaceuticals, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
9954 Maryland Drive, Deep Run Iii Ste. 4000, Richmond, Virginia 23233

Distribution

Quantity
113 bottles
Distribution pattern
Nationwide in the USA.

Timeline

Recall initiated
2022-06-29
FDA classified
2022-08-05
Posted by FDA
2022-08-17
Terminated
2024-02-13
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1323-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.