Class II · Moderate risk Ongoing
Renew Skin Repair Cream
Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
READYFLUSH PROTECT with Dimethicone
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Microbial Contamination of a Non-Sterile Product.
What was recalled
READYFLUSH PROTECT with Dimethicone (3.2%), Flushable Personal Cleaning Cloths, 24-count flexible pack. Manufactured by Medline Industries, Inc. Mundelein, IL 60060 USA. NDC 53329-066-58.
- Recalling firm
- Medline Industries Inc (Northpoint Services)
- NDC code
- 53329-066-58
- Origin
- IL, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0855-2018
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 Dimethicone recalls
See all
Class II · Moderate risk Ongoing
Renew PeriProtect
Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Class II · Moderate risk Ongoing
4-N-1 Skin Protectant
Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Class II · Moderate risk Ongoing
Oatmeal Daily Moisturizing Body Lotion
Reason Microbial Contamination of Non-Sterile Products: confirmed presence of mold contamination
Class II · Moderate risk Terminated
LA FRESH travel lite Sunnyside Lotion Wipe silky
Reason Marketed without an Approved NDA/ANDA: The product may be construed a sunscreen due to labeling of the product and comments about the product found on e-commerce websites.
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.