[Recalled] Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9 — Mis-packaging | FDA 2018-12-13
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9 |
|---|---|
| Brand / manufacturer | ProThera, Inc. dba SFI USA |
| Category | food |
| Issuing authority | FDA_FOOD |
| Reference | F-1186-2019 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 13 December 2018 |
| EAN / barcode | 2018210303 |
Why it was recalled
According to the FDA_FOOD notice, the identified hazard is: Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.
This Class II recall concerns food products distributed in United States and was recorded by FDA_FOOD. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from ProThera, Inc. dba SFI USA
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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