FDAOctober 17, 2023device
Lugol s Iodine Solution 500ML, Part Number 624-71
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Due to the incorrect packaging utilized with lot 3124, there' s an improper seal between the cap and bottle. With an improper seal the Assay (current specification of 24.8 to 27.2 mL) is expected to continue to drop over time as iodine vapors continue to dissipate from the bottles.
What to do
FDA enforcement status: Ongoing
Brands named
emd milliporeemd
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDASchiff Reagent, Hotchkiss-McManus, packaged in an amber glass bottle with a black polypropylene cap.2024-01-26
- FDACetrotide (cetrorelix acetate for Injection) 0.25 mg, Sterile - for subcutaneous use only, Rx Only, Manufactured for: EMD Serono, Inc., Rockland, MD 02370, NDC: 44087-1225-12020-06-29
- FDAMinicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon CS-15) Minicon concentrators are non-sterile, disposable, multiwall ultrafiltration devices. Minicon¿ clinical sample concentrators are for in vitro diagnostic use and are intended ...2018-05-14
- FDAClomiPHENE CITRATE Tablets, USP, 50 mg, 10-count (2 foil sealed plastic trays of 5 tablets each) per carton, Rx only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD., Jerusalem, 91010, Israel; Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960; NDC 0093-0041-03, UPC 3 009...2015-09-10
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