Food recall: Colon Rebuild I (90 capsules), 2boxes x 240 bottles, 1box x 200 bottles.
Class II FDA enforcement event 67491. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw ingredient that was on recalled by Specialty Enzymes & Biotechnologies due to chloramphenicol.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Global Vitality, Inc. dba Enzyme Process International started this food recall on 22 Oct 2013. The firm address in the FDA record is in Chandler, AZ. FDA put the recall in Class II. FDA event 67491 has 9 product records. The first FDA enforcement report date is 19 Mar 2014. The record gives the status Terminated, with the termination date 5 Nov 2014.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
PA, AZ, HI,
Recalling firm
Global Vitality, Inc. dba Enzyme Process International, Chandler, AZ.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
9 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1635-2014 | Colon Rebuild I (90 capsules), 2boxes x 240 bottles, 1box x 200 bottles. | 63,180 units | Class II | Terminated | 19 Mar 2014 |
| F-1636-2014 | Fat Sugar (bulk), 3 boxes x 12 kg, 1 box x 8.76 kg. | 100,000 units | Class II | Terminated | 19 Mar 2014 |
| F-1637-2014 | Adrenal Support (bulk), 4 boxes x 12 kg, 1 box x 11.48 kg. | 99,133 units | Class II | Terminated | 19 Mar 2014 |
| F-1638-2014 | Energy Clarity (bulk), 6 boxes x 15 kg, 1 box x 10.55 kg. | 100,000 units | Class II | Terminated | 19 Mar 2014 |
| F-1639-2014 | Multi Vitamin (bulk), 6 boxes x 12 kg, 1 box x 5.5kg. | 100,000 units | Class II | Terminated | 19 Mar 2014 |
| F-1640-2014 | Total Digestion, Lot 1635, 4 boxes x 9.92 kg. Lot 1841, 4 boxes x 12 kg, 1 box x 11.24 kg. Lot 2017, 3 boxes x 10 kg, 1 box x 9.32 kg. | 348,300 units | Class II | Terminated | 19 Mar 2014 |
| F-1641-2014 | Pain Power, 100 vegetarian capsules, 55 boxes x 72 bottles, 1 box x 7 bottles. | 244,800 units | Class II | Terminated | 19 Mar 2014 |
| F-1642-2014 | Super Digestayme, 200 count, 2 boxes x 72 bottles, 1 box x 55 bottles. 300 count, 4 boxes x 72 bottles, 1 box x 12 bottles. | 69,800 units | Class II | Terminated | 19 Mar 2014 |
| F-1643-2014 | Colon Rebuild II, 210 capsules, 6 boxes x 72 bottles, 1 box x 70 bottles. | 105,420 units | Class II | Terminated | 19 Mar 2014 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Food events that started in 2013
- 546
- Share of these events in Class II
- 52%
- Product records in this event
- 9
- Events of the firm on the register
- 1
Official channels
- FDA enforcement report F-1635-2014The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 67491. https://recallregister.com/fda/ii/67491/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
PA, AZ, HI,
- What quantity of product is in FDA event 67491?
- The event has 9 product records. The first record gives this quantity:
63,180 units
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2013 have the same class?
- 52% of the 546 food events that started in 2013 are in Class II.