Similac Special Care 2 fl oz reclose able plastic bottle Packaged as: 4 count carton
Summary
The FDA issued a Class II for Similac Special Care 2 fl oz reclose able plastic bottle Packaged as: 4 count c by Abbott Laboratories. Reason: Compromised seal integrity which could lead to spoilage.
Details
Source
Food Recall
External ID
F-0162-2023
Action Date
2022-11-23
Status
Terminated
Category
food
Product Description
Similac Special Care 2 fl oz reclose able plastic bottle Packaged as: 4 count carton
Lot/Code Info: Batch No. 41861N200 Case No. 440344R00 Product No. 67446 Best By 06/01/23
Quantity Affected: 14,588,544 bottles TOTAL
Reason for Recall
Compromised seal integrity which could lead to spoilage
Distribution
Domestic: Alaska, Alabama, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maine, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Washington DC, Wisconsin, West Virginia, Wyoming Foreign: Canada, Puerto Rico, Bermuda, Curacao, Trinidad, Tobago, Panama, Dominican Republic, and Colombia
Type: Voluntary: Firm initiated
Recall Initiated: 2022-10-13
Company
Columbus, OH
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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Abbott Laboratories has 101 FDA actions in our database, including 86 recalls and 15 clearances.
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 (Abbott Laboratories) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Abbott Laboratories have FDA actions?
Abbott Laboratories has 101 FDA actions in our database, including 86 recalls and 15 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0162-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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