CLASS II Food recall · Reported 2 Nov 2016 · FDA Enforcement Report

CertaVite with Antioxidants recalled by Pharmatech

Pharmatech is recalling CertaVite with Antioxidants, distributed in Florida, Michigan, Mississippi, Ohio. The recall was initiated on 8 Aug 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesNDC No. 0904-5023-09; Lot No. 20471602, Exp. Date 01/2018; Lot No. 20471603 & 20471604, Exp. Date 02/2018; Lot No. 20471605 & 20171606, Exp. Date 03/2018; Lot No. 20471607, Exp. Date 04/2018; Lot No. 20471609, 20471611& 20471612, Exp. Date 05/2018.
Quantity recalled110,136 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0265-2017
FDA event ID
75272
Recalling firm
Pharmatech, Davie, FL
Classification
Class II
Status
Terminated
Recall initiated
8 Aug 2016
FDA classified
25 Oct 2016
Reported
2 Nov 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility
Product category
Dietary Supplements

Timeline

8 Aug 2016Recall initiated by company
25 Oct 2016Classified by FDA+78 days
2 Nov 2016Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

CertaVite with Antioxidants, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.

Where it was distributed

FL, MI, MS, and OH.

FloridaMichiganMississippiOhio

Questions about this recall

Is CertaVite with Antioxidants recalled?

Yes. Pharmatech recalled CertaVite with Antioxidants on 8 Aug 2016. The recall is Class II and its status is Terminated. Recall number F-0265-2017.

Why was it recalled?

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Which lots are affected?

NDC No. 0904-5023-09; Lot No. 20471602, Exp. Date 01/2018; Lot No. 20471603 & 20471604, Exp. Date 02/2018; Lot No. 20471605 & 20171606, Exp. Date 03/2018; Lot No. 20471607, Exp. Date 04/2018; Lot No. 20471609, 20471611& 20471612, Exp. Date 05/2018.

Where was it sold?

FL, MI, MS, and OH.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Pharmatech

All 53
ReportedClassRecallCompanyReasonWhere
FoodCLASS IIRugby Poly-Vitamin w/ Iron Liquid recalled by PharmatechRugby Poly-VitaminPharmatechMoldMI
FoodCLASS IIRugby Cerovite Liquid recalled by PharmatechRugby CerovitePharmatechMoldMI
FoodCLASS IIMajor Poly-Vita Drops w/ Iron recalled by PharmatechMajor Poly-VitaPharmatechMoldMI
FoodCLASS IIRugby Liquid Vitamin C Supplement 500 mg recalled by PharmatechRugbyPharmatechMoldMI
FoodCLASS IIRugby Tri-Vitamin Liquid recalled by PharmatechRugby Tri-VitaminPharmatechMoldMI

Other Dietary Supplements recalls

All 733