FDA recall record

Strong Iodine Solution U.S.P. (Lugol's Solution) (Iodine 5%), 14 mL Glass Dropper bottle in recall — FDA D-0082-2024

CGMP Deviations: Recall due to the absence of USP CGMP compendial requirements.

Class IIclassification
D-0082-2024official record ID
Nov 8, 2023report date

Recall record at a glance

Official recordD-0082-2024
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSafecor Health, LLC
Report dateNov 8, 2023
Recall initiation dateOct 19, 2023
Quantity166,022 bottles
LocationWoburn, MA, United States

Official product description

Strong Iodine Solution U.S.P. (Lugol's Solution) (Iodine 5%), 14 mL Glass Dropper bottle in box, RX only, Safecor Health, LLC, Woburn, MA 01801. NDC# 48433-230-15

Why the product was recalled

CGMP Deviations: Recall due to the absence of USP CGMP compendial requirements.

Distribution information

Distributed Nationwide in the USA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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