JIF NO ADDED SUGAR PEANUT BUTTER packaged in 15.5oz and 46.5oz
Summary
The FDA issued a Class I for JIF NO ADDED SUGAR PEANUT BUTTER packaged in 15.5oz and 46.5oz by The JM Smucker Company LLC. Reason: Products are potentially contaminated with Salmonella..
Details
Source
Food Recall
External ID
F-1120-2022
Action Date
2022-06-08
Status
Terminated
Category
food
Product Description
JIF NO ADDED SUGAR PEANUT BUTTER packaged in 15.5oz and 46.5oz
Lot/Code Info: Lot codes: 1274425 2140425 UPC: 5150024540, 5150041418 Best By Date: 10/01/22 - 05/20/23
Quantity Affected: 115,106 cases total
Reason for Recall
Products are potentially contaminated with Salmonella.
Distribution
AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, WV, WY
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-20
Company
Orrville, OH
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 76 food recalls issued in the same week, part of 204 food-related FDA actions this month.
The JM Smucker Company LLC has 26 FDA actions in our database, including 26 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 (The JM Smucker Company LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The JM Smucker Company LLC have FDA actions?
The JM Smucker Company LLC has 26 FDA actions in our database, including 26 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1120-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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