CLASS III Food recall · Reported 5 Jul 2023 · FDA Enforcement Report

Vit-ra-tox Calphonite #38 in an amber recalled by Anatox

Anatox is recalling Vit-ra-tox Calphonite #38 in an amber, distributed in 27 states. The recall was initiated on 26 May 2023 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codes1. 030724-1; 030824-2; 030824-3; 040524-1; 040624-2; 051024-1; 051124-2 2. 030924-4; 031024-5; 080824-1
Quantity recalled6,777 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-1005-2023
FDA event ID
92186
Recalling firm
Anatox, Richland, MO
Classification
Class III
Status
Terminated
Recall initiated
26 May 2023
FDA classified
23 Jun 2023
Reported
5 Jul 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Foreign Material
Product category
Other

Timeline

26 May 2023Recall initiated by company
23 Jun 2023Classified by FDA+28 days
5 Jul 2023Published in enforcement report+12 days

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

Reason for recall

Elevated lead levels

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

1. VIT-RA-TOX Calphonite #38, 15 Fl. oz. (444 ml) in an amber glass bottle; 2. Sonne's Calphonite #2, 15 Fl. oz. (444 ml) in an amber glass bottle

Where it was distributed

Distributors, retailers, and consumers in AL, AZ, CA, CT, CO, FL, GA, IL, IN, KS, KY, MA, MD, MN, MO, NC, NM, NY, OH, OR, PA, TN, TX, UT, VA, VT, WI

AlabamaArizonaCaliforniaColoradoConnecticutFloridaGeorgiaIllinoisIndianaKansasKentuckyMassachusettsMarylandMinnesotaMissouriNorth CarolinaNew MexicoNew YorkOhioOregon

Questions about this recall

Is Vit-ra-tox Calphonite #38 in an amber recalled?

Yes. Anatox recalled Vit-ra-tox Calphonite #38 in an amber on 26 May 2023. The recall is Class III and its status is Terminated. Recall number F-1005-2023.

Why was it recalled?

Elevated lead levels

Which lots are affected?

1. 030724-1; 030824-2; 030824-3; 040524-1; 040624-2; 051024-1; 051124-2 2. 030924-4; 031024-5; 080824-1

Where was it sold?

Distributors, retailers, and consumers in AL, AZ, CA, CT, CO, FL, GA, IL, IN, KS, KY, MA, MD, MN, MO, NC, NM, NY, OH, OR, PA, TN, TX, UT, VA, VT, WI

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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 Anatox

All 2
ReportedClassRecallCompanyReasonWhere
FoodCLASS IIISonne's Detoxificant #7 recalled by AnatoxSonne's DetoxificantAnatoxForeign Material27 states

Other Other recalls

All 4,664