Stainless Steel Water Bottle The product comes in four sizes: 32 oz., 24 oz., 20 oz., and 13 oz.
Summary
The FDA issued a Class II for Stainless Steel Water Bottle The product comes in four sizes: 32 oz., 24 oz., 20 by BINDLE BOTTLE. Reason: Water bottle has a cup with a screw cap attached by a weld that has been found to leach lead..
Details
Source
Food Recall
External ID
F-0685-2023
Action Date
2023-04-05
Status
Terminated
Category
food
Product Description
Stainless Steel Water Bottle The product comes in four sizes: 32 oz., 24 oz., 20 oz., and 13 oz.
Lot/Code Info: No code on bottle
Quantity Affected: 203,523 units
Reason for Recall
Water bottle has a cup with a screw cap attached by a weld that has been found to leach lead.
Distribution
Distributed to customers directly via online sales and distributors nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-17
Company
Encinitas, CA
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 66 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (BINDLE BOTTLE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does BINDLE BOTTLE have FDA actions?
This is the only FDA action we have on record for BINDLE BOTTLE in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0685-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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