Recalls / Class I
Class IF-1256-2023
Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.
Product
Pineapple Chunks packaged under the following brand names and sizes. 1. 365 Whole Foods Market, Net Wt 16 oz (1 lb) 454g UPC 0 99482-40854 1. Keep Frozen. Distributed by: Whole Foods Market, Austin, TX 78703. 2. 365 Whole Foods Market, Net Wt 10 oz (284g) UPC 0 99482-49096 6. Keep Frozen. Distributed by: Whole Foods Market, Austin, TX 78703. 3. Bulk Organic Pineapple Chunks, Sunrise Item 4510-000, Net Wt 30 lb. Product of Mexico.
- Type
- Food
- Affected lot / code info
- 1. Lot / Best By: FED303132 / 01/31/2025; FED303231 / 02/01/2025; FED307532 / 03/16/2025; FED303133 / 01/31/2025; FED303431 / 02/03/2025; FED307631 / 03/17/2025 2. Lot / Best By: FED303011 / 01/30/2025; FED303131 / 01/31/2025; FED311631 / 04/26/2025; FED303111 / 01/31/2025; FED307531 / 03/16/2025; FED225511 / 09/12/2024; FED225611 / 09/13/2024; FED225711 / 09/14/2024; FED225811 / 09/15/2024. 3. Lot: 8FQ221302000MX, 8FQ222202000MX, 8FQ222302000MX, 8FQ225502000MX, 8FQ225702000MX, 8FQ228302000MX, 8FQ228402000MX, 8FQ229702000MX, 8FQ229902000MX, 8FQ230402000MX, 8FQ231102000MX, 8FQ231202000MX, 8FQ234402000MX, 8FQ235502000MX, 8FQ235602000MX, 8FQ236302000MX, 8FQ300202000MX, 8FQ308602000MX.
- Quantity
- 22995 cases + 232,300 lbs. bulk
Why it was recalled
Fruit products have the potential to be contaminated with Listeria monocytogenes.
Recalling firm
- Firm
- SunOpta Grains and Foods Inc.
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 7078 Shady Oak Rd, N/A, Eden Prairie, Minnesota 55344-3505
Distribution
- Distribution pattern
- Nationwide
Timeline
- Recall initiated
- 2023-06-16
- FDA classified
- 2023-07-18
- Posted by FDA
- 2023-07-26
- Terminated
- 2024-02-07
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-1256-2023. The FDA issues recall classifications as health-hazard assessments, not legal findings.