FDA Recall United States Terminated Historical recordClass I
David Oppenheimer & Company I LLC
- Product
- Zespri Organic Green Kiwi, product of New Zealand, one palle…
- Published
- September 20, 2023
- Distribution
- Distributed in FL, GA, IL, IN, KY, MI, N…
David Oppenheimer & Company I LLC Recall: Listeria monocytogenes
United States
TerminatedClass I
- Company
- David Oppenheimer & Company I LLC
- Product
- Zespri Organic Green Kiwi, product of New Zealand, perishabl…
- Recall date
- August 8, 2023
- Terminated
- October 20, 2023
- Source
- FDA
Reason for recall
Listeria monocytogenes
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Zespri Organic Green Kiwi, product of New Zealand, perishable, packaged in plastic clamshell, net wt. 1lb. UPC 818849020093. Distributed by The Oppenheimer Group, 180 Nickerson Street, Suite 211 Seattle WA. Zespri Organic Green Kiwi, product of New Zealand, perishable, packaged in plastic clamshell, net wt. 3lb, item #7953. | 818849020093 | 4568 cases (12/1lb. containers per case); 332 cases (6/3lb. containers per case) | No codes on retail 1lb. or 3lb.s plastic clamshell container. Oppenheimer lot code on the master carton: WO00278238. Non-recall product in 1lb or 3lb. clamshell container will include a white sticker with the packed-on date and the work order number. |
Distribution
- Distributed in FL
- GA
- IL
- IN
- KY
- MI
- NC
- NY
- OH
- PA
- TN
- TX
- VA
- and WI.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1494-2023
- Event ID
- 92830
- Status
- Terminated
- Classification
- Class I
- Company
- David Oppenheimer & Company I LLC
- Product description
- Zespri Organic Green Kiwi, product of New Zealand, perishable, packaged in plastic clamshell, net wt. 1lb. UPC 818849020093. Distributed by The Oppenheimer Group, 180 Nickerson Street, Suite 211 Seattle WA. Zespri Organic Green Kiwi, product of New Zealand, perishable, packaged in plastic clamshell, net wt. 3lb, item #7953.
- Quantity
- 4568 cases (12/1lb. containers per case); 332 cases (6/3lb. containers per case)
- Reason
- Listeria monocytogenes
- Recall initiation date
- August 8, 2023
- Report date
- September 20, 2023
- Classification date
- Not published in this source record
- Termination date
- October 20, 2023
- Distribution pattern
- Distributed in FL, GA, IL, IN, KY, MI, NC, NY, OH, PA, TN, TX, VA, and WI.
- UPC, lot, and code information
- UPC 818849020093; No codes on retail 1lb. or 3lb.s plastic clamshell container. Oppenheimer lot code on the master carton: WO00278238. Non-recall product in 1lb or 3lb. clamshell container will include a white sticker with the packed-on date and the work order number.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 92830 with 1 other product entry in Public Health Trace.
Responsible company: David Oppenheimer & Company I LLC
Other recalls from David Oppenheimer & Company I LLC
FDA Recall United States Terminated Historical recordClass I
David Oppenheimer & Company I LLC
- Product
- Zespri Organic Green Kiwi, product of New Zealand, one palle…
- Published
- September 20, 2023
- Distribution
- Distributed in FL, GA, IL, IN, KY, MI, N…
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Florida | 1 |
| Georgia | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kentucky | 1 |
| Michigan | 1 |
| North Carolina | 1 |
| New York | 1 |
| Ohio | 1 |
| Pennsylvania | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Virginia | 1 |
| Wisconsin | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
