Class IITerminated · reported 2015-04-08

TonicCare II

Health One Pharmaceuticals Inc recalled this product and the FDA reported the enforcement action on 8 April 2015 as Class II. The recall was initiated by the firm. Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.

The record

Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.

Product
TonicCare II
Reason for recall
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Firm location
City Of Industry, California, United States
Classification
Class II
Status
Terminated
Recall number
F-1645-2015
Quantity
135,000 units
Distribution
Nationwide in US: CA, TN, WA, ID, and worldwide: Hong Kong, Vietnam, China, Singapore
Initiated
4 February 2015
Reported by FDA
8 April 2015
Terminated
31 March 2015
Firm notified by
Letter
Product codes
2613

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

  • Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
  • The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
  • This is one of 147 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 147 separate recalls, which almost every published figure does, overstates it by a factor of 147. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 147 of them.
  • The recall ran for 8 weeks, from 4 February 2015 to termination on 31 March 2015. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
  • The distribution pattern names 3 states, and the FDA published the enforcement report 2 months after the firm began the recall.
  • The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.

Named in the distribution pattern: Tennessee, Washington, Idaho. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.

Other records from Health One Pharmaceuticals Inc

The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 146 other records name this firm.

ReportedProductFirmReasonClass
2015-04-08EST -700 CalciumHealth One Pharmaceuticals IncHealth One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.Class II
2015-04-08SOD Herbal MixHealth One Pharmaceuticals IncHealth One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.Class II
2015-04-08Femanol, 60 capsules, 500mgHealth One Pharmaceuticals IncHealth One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.Class II
2015-04-08Bone Rebuilder, 120 tabletsHealth One Pharmaceuticals IncHealth One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.Class II
2015-04-08Fish CollagenHealth One Pharmaceuticals IncHealth One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.Class II
2015-04-08All Tonic, 80 Veggie Capsules, 400 mgHealth One Pharmaceuticals IncHealth One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.Class II
2015-04-08Slimin, 80 Veggie Capsules, 400 mgHealth One Pharmaceuticals IncHealth One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.Class II
2015-04-08Nikente Astaxanthin Bilberry, 60 Capsules, 30g.Health One Pharmaceuticals IncHealth One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.Class II
2015-04-08Slim Formula, 90 capsules, 500mgHealth One Pharmaceuticals IncHealth One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.Class II
2015-04-08MilCalHealth One Pharmaceuticals IncHealth One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.Class II

All 147 records for Health One Pharmaceuticals Inc

All 2015 recalls · All FDA food recall data

Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.