CertaVite with Antioxidants, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0265-2017.
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0265-2017.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Pharmatech Llc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0265-2017.
Pharmatech LLC
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Pharmatech Llc Recall FAQ
Pharmatech Llc is the subject of a supplements safety report: CertaVite with Antioxidants, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.. The notice was published on August 8, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 110,136 units are potentially affected.