Class II · Moderate risk Ongoing
Suave Inv Sld Pwdr 1.2 Oz Sku2004504 Suave Ap Inv Solid Sweet…
Reason CGMP Deviations: product held outside appropriate storage temperature conditions.
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
What was recalled
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48240-4, Shade 05 (D-G)
- Recalling firm
- Clinique International
- Origin
- NY, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1477-2016
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 Paris recalls
See all
Class II · Moderate risk Terminated
Desmopressin Acetate Tablets
Reason GMP Deviations: Product bottle may be absent of desiccant.
Class II · Moderate risk Terminated
Desmopressin Acetate Tablets
Reason GMP Deviations: Product bottle may be absent of desiccant.
Class III · Low risk Terminated
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15
Reason Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Class III · Low risk Terminated
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15
Reason Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Get an alert if your medication is recalled
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.