Food recall: Promote with Fiber Vanilla, 8oz metal can
Class II FDA enforcement event 76167. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
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
Abbott Nutrition started this food recall on 9 May 2016. The firm address in the FDA record is in Altavista, VA. FDA put the recall in Class II. FDA event 76167 has 6 product records. The first FDA enforcement report date is 8 Feb 2017. The record gives the status Terminated, with the termination date 31 Jan 2017.
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.
The product was distributed in the US as well as the following foreign countries: Guam and Puerto Rico, Israel, Kuwait, Trinidad and Tobago
Recalling firm
Abbott Nutrition, Altavista, VA.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
6 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1419-2017 | Promote with Fiber Vanilla, 8oz metal can | 262,608 units | Class II | Terminated | 8 Feb 2017 |
| F-1420-2017 | Oxepa, 8oz metal can | 45,156 units | Class II | Terminated | 8 Feb 2017 |
| F-1421-2017 | Nepro Vanilla High Protein , 8oz metal can | 37,584 units | Class II | Terminated | 8 Feb 2017 |
| F-1422-2017 | Nepro Vanilla , 8oz metal can | 332,088 units | Class II | Terminated | 8 Feb 2017 |
| F-1423-2017 | Vital High Protein, 8oz metal can | 31,440 units | Class II | Terminated | 8 Feb 2017 |
| F-1424-2017 | Nepro Mixed Berry, 8oz metal can | 362,400 units | Class II | Terminated | 8 Feb 2017 |
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 2016
- 799
- Share of these events in Class II
- 43%
- Product records in this event
- 6Median of the firm: 1
- Events of the firm on the register
- 4
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 16 Aug 2022 | Similac Alimentum packaged in 32 fluid ounce re-closable plastic bottles 6 bottles per case | Food | Class II | 1 |
| 10 Mar 2016 | The product is labeled as follows: PediaSure Grow & Gain Vanilla, Unit size : 8 oz. , Container description : Metal Can, | Food | Class II | 1 |
| 11 Oct 2013 | Similac Human Milk Fortifier Powder, .9 g packets. Label reads in part, "ADDITIONAL IRON MAY BE NECESSARY ADD ONLY TO HU | Food | Class II | 1 |
Official channels
- FDA enforcement report F-1419-2017The 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 76167. https://recallregister.com/fda/ii/76167/. 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:
The product was distributed in the US as well as the following foreign countries: Guam and Puerto Rico, Israel, Kuwait, Trinidad and Tobago
- What quantity of product is in FDA event 76167?
- The event has 6 product records. The first record gives this quantity:
262,608 units
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2016 have the same class?
- 43% of the 799 food events that started in 2016 are in Class II.