FDA Recall Terminated Historical recordClass II
N-A-C (N-Acetyl-L-Cysteine, 500 mg, 100 capsules; Veggie Caps, white HDPE bottle with RED label Product # 107002 UPC: 790011070023
- Published
- November 4, 2020
- Distribution
- Nationwide
Jarrow Formulas Inc Recall: A higher than normal micro result was found at the six month time point for one lot of Liquid L-Carnitine.
United States
TerminatedClass II
- Company
- Jarrow Formulas Inc
- Product
- Jarrow Formulas Liquid L-Carnitine; 16 fl oz. (475 ml) bott…
- Recall date
- January 15, 2018
- Terminated
- July 10, 2018
- Source
- FDA
Reason for recall
A higher than normal micro result was found at the six month time point for one lot of Liquid L-Carnitine.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Jarrow Formulas Liquid L-Carnitine; 16 fl oz. (475 ml) bottle, dietary supplement; product number 102006; UPC 7 90011 02006 6; Vitamin B5 10 mg; L-Carnitine 1000 mg; Other ingredients: Purified water, xylitol, glycerin, citric acid, natural lemon-lime flavor, nisin (as a preservative). Distributed exclusively by Jarrow Formulas Los Angeles, CA. | Not published in this source record | 2853 units | Lot Number: JLC17131; Expiration date: 05/2019 |
Distribution
- Nationwide distribution
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0682-2018
- Event ID
- 78967
- Status
- Terminated
- Classification
- Class II
- Company
- Jarrow Formulas Inc
- Product description
- Jarrow Formulas Liquid L-Carnitine; 16 fl oz. (475 ml) bottle, dietary supplement; product number 102006; UPC 7 90011 02006 6; Vitamin B5 10 mg; L-Carnitine 1000 mg; Other ingredients: Purified water, xylitol, glycerin, citric acid, natural lemon-lime flavor, nisin (as a preservative). Distributed exclusively by Jarrow Formulas Los Angeles, CA.
- Quantity
- 2853 units
- Reason
- A higher than normal micro result was found at the six month time point for one lot of Liquid L-Carnitine.
- Recall initiation date
- January 15, 2018
- Report date
- February 7, 2018
- Classification date
- Not published in this source record
- Termination date
- July 10, 2018
- Distribution pattern
- Nationwide distribution
- UPC, lot, and code information
- Lot Number: JLC17131; Expiration date: 05/2019
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Jarrow Formulas Inc
Other recalls from Jarrow Formulas Inc
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
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?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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