Revie Superfoods Strawberry Zen 222g Ready-to-Blend Strawberry Banana Smoothie Made in…
Revive Organics, Inc. recalled this product and the FDA reported the enforcement action on 27 July 2022 as Class II. The recall was initiated by the firm. Potential norovirus from IQF raspberries that were used as an ingredient in the products.
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
- Revie Superfoods Strawberry Zen 222g Ready-to-Blend Strawberry Banana Smoothie Made in Canada UPC 8 54681 00003 9 Revive Superfoods 1880 Bonhill Road, Mississauga, Ontario, Canada
- UPC
- 854681000039
- Reason for recall
- Potential norovirus from IQF raspberries that were used as an ingredient in the products.
- Recalling firm
- Revive Organics, Inc.
- Firm location
- Oakville, N/A, Canada
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-1435-2022
- Quantity
- 57,960 units (total)
- Distribution
- U.S. distribution to distributors located in PA, CA, IL, and TX who further distributed directly to consumers.
- Initiated
- 11 June 2022
- Reported by FDA
- 27 July 2022
- Terminated
- 28 February 2023
- Firm notified by
- Product codes
- Lot numbers -1010422, 1090422, 1100422, 1260522, 1290522, 1320522, 1180422, 1020422, 1110422, 1230522, 1030422, 1170422, 1250522, 1240522
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 7 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 7 separate recalls, which almost every published figure does, overstates it by a factor of 7. All 7 of them are listed on this page.
- The recall ran for 9 months, from 11 June 2022 to termination on 28 February 2023. 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 2 states, and the FDA published the enforcement report 7 weeks after the firm began the recall.
- Recalls of fresh produce run a median of 7 months, so this one was longer than usual for its category. Fresh produce is the category where contamination arrives before the facility does: irrigation water, soil amendments and field workers are the routes, and nothing downstream of the farm is a kill step for a product eaten raw.
Named in the distribution pattern: California, Illinois. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Viral and parasitic contamination
Hepatitis A, norovirus and Cyclospora recalls trace back to a person or to water rather than to the process: an infected food handler, or produce irrigated or washed with contaminated water.
A preventive controls plan covers viral or parasitic contamination under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.10
- Personnel: the hygiene practices, and the exclusion of anyone with an illness or open lesion that could contaminate food, that a facility must require.
- 21 CFR 112
- Produce safety: the agricultural water, worker health and hygiene standards for farms growing produce eaten raw.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
Filed under fresh produce and beverages and juice. A product can sit in more than one.
Every product in this recall
The FDA opened 7 enforcement records for this one recall, one per product code. This page carries all of them; the 6 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
Other fresh produce recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Revive Organics, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 6 other records name this firm.
All 7 records for Revive Organics, Inc.
All 2022 recalls · All FDA food recall data
21 CFR 117.10 is the clause behind this recall, and it is one 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 accessRecall 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.