Zespri Organic Green Kiwi, product of New Zealand, perishable, packaged in plastic clamshell, net wt. 1lb. UPC 818849020
Summary
The FDA issued a Class I for Zespri Organic Green Kiwi, product of New Zealand, perishable, packaged in plast by David Oppenheimer & Company I LLC. Reason: Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-1494-2023
Action Date
2023-09-20
Status
Terminated
Category
food
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.
Lot/Code Info: 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.
Quantity Affected: 4568 cases (12/1lb. containers per case); 332 cases (6/3lb. containers per case)
Reason for Recall
Listeria monocytogenes
Distribution
Distributed in FL, GA, IL, IN, KY, MI, NC, NY, OH, PA, TN, TX, VA, and WI.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-08
Company
Seattle, WA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.
David Oppenheimer & Company I LLC has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (David Oppenheimer & Company I LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does David Oppenheimer & Company I LLC have FDA actions?
David Oppenheimer & Company I LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1494-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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