Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor, 15000 mcg, Dietary Supplement 29 doses 1 fl oz (29mL) UPC:
Summary
The FDA issued a Class II for Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor, 15000 mcg, Dietary by BioMylz Pvt. Ltd.. Reason: Potential mold contamination.
Details
Source
Food Recall
External ID
F-0664-2024
Action Date
2024-01-10
Status
Terminated
Category
food
Product Description
Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor, 15000 mcg, Dietary Supplement 29 doses 1 fl oz (29mL) UPC: 194346065158 Packaged in a glass bottle in a paper carton
Lot/Code Info: NSBS2301, NSBS2302, NSBS2303, NSBS2306, NSBS2308
Quantity Affected: 24,324 units
Reason for Recall
Potential mold contamination
Distribution
Distributed to a distribution center in CA and then further distributed to distribution centers and retail stores nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-12-01
Company
Bengaluru, N/A
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 12 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 (BioMylz Pvt. Ltd.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does BioMylz Pvt. Ltd. have FDA actions?
This is the only FDA action we have on record for BioMylz Pvt. Ltd. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0664-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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