SKIPPY Creamy Peanut Butter Blended with Plant Protein NET WT 14 (397 g) UPC 037600880954 packaged in clear plastic jar
Summary
The FDA issued a Class II for SKIPPY Creamy Peanut Butter Blended with Plant Protein NET WT 14 (397 g) UPC 037 by Skippy Foods, LLC.. Reason: Potential to contain small steel contaminants..
Details
Source
Food Recall
External ID
F-0997-2022
Action Date
2022-04-20
Status
Terminated
Category
food
Product Description
SKIPPY Creamy Peanut Butter Blended with Plant Protein NET WT 14 (397 g) UPC 037600880954 packaged in clear plastic jar with black label
Lot/Code Info: Best if Used By MAY1023
Quantity Affected: 9,353 cases (total)
Reason for Recall
Potential to contain small steel contaminants.
Distribution
CA, CT, DE, FL, HI, IL, IN, KS, MA, ME, MN, MO, NC, NE, NH, NJ, NY, OK, OR, PA, WI and Mexico (None of the recalled product made it to customers in MX)
Type: Voluntary: Firm initiated
Recall Initiated: 2022-03-30
Company
Little Rock, AR
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 40 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Skippy Foods, LLC. has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Skippy Foods, LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Skippy Foods, LLC. have FDA actions?
Skippy Foods, LLC. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0997-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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