bloommy Inc. Recall: Dietary supplement contains undeclared fish collagen - F-0542-2021
United States
TerminatedClass II
- Company
- bloommy Inc.
- Product
- "Bloomy*** Biotin Collagen Keratin***Capsules for SKIN, JOIN…
- Recall date
- May 4, 2021
- Terminated
- January 31, 2022
- Source
- FDA
Reason for recall
Dietary supplement contains undeclared fish collagen
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| "Bloomy*** Biotin Collagen Keratin***Capsules for SKIN, JOINT, HAIR***Supplement Facts***Marine Collagen***Manufactured for Bloommy Inc. 106 W. Broad St. Pawcatuck, CT 06379" | Not published in this source record | 74598 units | all codes |
Distribution
- Nationwide through e-commerce
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0542-2021
- Event ID
- 87858
- Status
- Terminated
- Classification
- Class II
- Company
- bloommy Inc.
- Product description
- "Bloomy*** Biotin Collagen Keratin***Capsules for SKIN, JOINT, HAIR***Supplement Facts***Marine Collagen***Manufactured for Bloommy Inc. 106 W. Broad St. Pawcatuck, CT 06379"
- Quantity
- 74598 units
- Reason
- Dietary supplement contains undeclared fish collagen
- Recall initiation date
- May 4, 2021
- Report date
- May 26, 2021
- Classification date
- Not published in this source record
- Termination date
- January 31, 2022
- Distribution pattern
- Nationwide through e-commerce
- UPC, lot, and code information
- all codes
- Voluntary or mandated
- N/A
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: bloommy Inc.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
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Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
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How to interpret this historical record
This record is preserved as published by FDA, as of January 31, 2022.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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