Severity
Moderate
ModerateActive
CPSC recall · Reported July 21, 2022
Vichy Laboratoires Recalls LiftActiv Peptide-C Ampoules Due to Laceration Hazard (Recall Alert)
The glass packaging of the small, sealed vials (ampoules) can weaken over time and break when opened, posing a laceration hazard to fingers and hands.
Cosmetique Active Internationale, of France recalled This recall involves Liftactiv Peptide-C Ampoules 1.8ml (10 pack) and Liftactiv Peptide-C… - a moderate-severity action.
Vichy Laboratoires Recalls LiftActiv Peptide-C Ampoules Due to Laceration Hazard (Recall … was recalled by Cosmetique Active Internationale, of France in July 21, 2022. Reason: The glass packaging of the small, sealed vials (ampoules) can weaken over time and break when opened, posing …. Remedy: Consumers should immediately stop using the recalled product and contact Vichy USA Consum…. Verify recall #22760 with the CPSC before acting.
The recall
Cosmetique Active Internationale, of France issued this moderate-severity CPSC recall-The glass packaging of the small, sealed vials (ampoules) can weaken over time and break when opened, posing ….
- Moderate
- severity level
- July 21, 2022
- reported
Sourced from official CPSC enforcement records. Verify recall #22760 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #22760) was formally reported on July 21, 2022. It is classified under Moderate severity, with a current status of Active. Cosmetique Active Internationale, of France is listed as the recalling firm. Federal records list the affected scope as About 206,200.
The documented reason for this recall is: The glass packaging of the small, sealed vials (ampoules) can weaken over time and break when opened, posing a laceration hazard to fingers and hands. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers should immediately stop using the recalled product and contact Vichy USA Consumer Care for a full refund. The firm is contacting all known purchasers. - consumers holding this product should act on that instruction rather than relying on general guidance.
Within the same product category the archive holds 6 closely related recalls, 6 from CPSC - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Household Products recalls over time
Where this recall sits in its category - 3,056 household products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
About 206,200
Related Recalls
6
6 from same agency
Product description
This recall involves Liftactiv Peptide-C Ampoules 1.8ml (10 pack) and Liftactiv Peptide-C Ampoules 1.8ml (30 pack) which are facial serums. The serum is packaged in amber-colored glass ampoules with the following batch numbers: 54T61Q, 54T91Q, 54TD1Q, 54TD2Q, 54TN1Q, 54TN2Q, 54TN3Q, 54TO1Q, 54U11Q, 54U12Q, 54U21Q, 54U31Q, 54U32Q, 54U41S, 54U42S, 54U51S, 54U52S, 54U53S, 54U54S, 54U61S, 54U72S, 54U91S, 54U62S, 54U92S, 54UD1S, 54UO1S, 54W11S, 54W12S, 54W13S, 54W21S. The batch number is printed on the bottom or side of the pack.
Reason for recall
The glass packaging of the small, sealed vials (ampoules) can weaken over time and break when opened, posing a laceration hazard to fingers and hands.
Remedy, what to do
Consumers should immediately stop using the recalled product and contact Vichy USA Consumer Care for a full refund. The firm is contacting all known purchasers.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 22760 |
| Date reported | July 21, 2022 |
| Date initiated | July 21, 2022 |
| Recalling firm | Cosmetique Active Internationale, of France |
| Affected scope | About 206,200 |
| Distribution | Not disclosed |
| Official source | CPSC notice → |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
What to do with this recall
Consumers should immediately stop using the recalled product and contact Vichy USA Consumer Care for a full refund. The firm is c…
- Check the recall number (22760) and product description against the item you own. Search the archive
- Confirm the current status and remedy on the official CPSC notice before acting. CPSC notice
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official CPSC record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
This recall involves Liftactiv Peptide-C Ampoules 1.8ml (10 pack) and Liftactiv Peptide-C Ampoules 1.8ml (30 pack) which are facial serums. The serum is packaged in amber-colored glass ampoules with the following batch numbers: 54T61Q, 54T91Q, 54TD1Q, 54TD2Q, 54TN1Q, 54TN2Q, 54TN3Q, 54TO1Q, 54U11Q, 54U12Q, 54U21Q, 54U31Q, 54U32Q, 54U41S, 54U42S, 54U51S, 54U52S, 54U53S, 54U54S, 54U61S, 54U72S, 54U91S, 54U62S, 54U92S, 54UD1S, 54UO1S, 54W11S, 54W12S, 54W13S, 54W21S. The batch number is printed on the bottom or side of the pack.. Recalled by Cosmetique Active Internationale, of France. Units affected: About 206,200.
Why was this product recalled? ▼
The glass packaging of the small, sealed vials (ampoules) can weaken over time and break when opened, posing a laceration hazard to fingers and hands.
What should consumers do? ▼
Consumers should immediately stop using the recalled product and contact Vichy USA Consumer Care for a full refund. The firm is contacting all known purchasers.
Which agency issued this recall? ▼
This recall was issued by the CPSC on July 21, 2022. Severity: Moderate. Recall number: 22760.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (22760) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product? ▼
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: CPSC, reported July 21, 2022. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.