Kit for the Preparation of Technetium Tc 99m Sulfur Colloid Injection
Failed Stability Specifications
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Superpotent: Drug product active ingredients were formulated incorrectly (too high) with respect to the label strength.
Cause type: Wrong potency / content
Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.
Sodium Sulfacetamide 10% and Sulfur 5% Lotion, (NDC 42792-102-01), 25 g Manufactured for: Austin Pharmaceuticals, LLC, Wilmington, DE
Compare with the code on your package — it is the most precise check available.
Drug: Sulfur
Low risk, still worth a check. Class III means the product is unlikely to cause harm but breaks an FDA rule (often labeling). If your lot matches, your pharmacy will normally swap it; there is no need for alarm. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.
Failed Stability Specifications
Subpotent drug
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Subpotent drug: Out of specification for assay at the end-of-shelf-life 24-month period.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Microbial Contamination of Non-Sterile Products: Product failed USP Microbial Limits Test.
Microbial Contamination of Non-Sterile Products: Product failed USP Microbial Limits Test.
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