Class II · Moderate risk Ongoing
Thyroid
Reason Subpotent Drug
Povidone Iodine
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of sterility assurance.
What was recalled
Povidone Iodine, 5% Ophthalmic Solution, 5 mL per droptainer, Repackaged by: Avella Specialty Pharmacy, 24416 N. 19th Ave., Phoenix, AZ 85085. NDC 42852-006-20
- Recalling firm
- Avella of Deer Valley, Inc. Store 38
- NDC code
- 42852-006-20
- Origin
- AZ, United States
- FDA recall number
- D-0152-2020
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Phoenix recalls
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Class II · Moderate risk Ongoing
edunn clarity
Reason Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Class II · Moderate risk Terminated
Bevacizumab
Reason Lack of Sterility Assurance
Class II · Moderate risk Completed
S.P Labs
Reason Failed Stability Specifications
Class II · Moderate risk Completed
S.P.Labs
Reason Failed Stability Specifications
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