CLASS II ONGOING Drug recall · Reported 2 Oct 2024 · FDA Enforcement Report
Vivier Sheer SPF 30 Mineral With Antioxidants recalled by Vivier Pharma
Vivier Pharma is recalling Vivier Sheer SPF 30 Mineral With Antioxidants (titanium dioxide 10% and zinc oxide 8%), distributed nationwide in the US. The recall was initiated on 3 Sep 2024 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0662-2024
- FDA event ID
- 95339
- Recalling firm
- Vivier Pharma, Vaudreuil-Dorion
- Brand
- Sheet Spf 30 Mineral
- Manufacturer
- Vivier Pharma Inc.
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 3 Sep 2024
- FDA classified
- 20 Sep 2024
- Reported
- 2 Oct 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
- Drug class
- Sunscreen & Personal Care
Timeline
| 3 Sep 2024 | Recall initiated by company | |
| 20 Sep 2024 | Classified by FDA | +17 days |
| 2 Oct 2024 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Microbial Contamination of Non-Sterile Product
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
Vivier Sheer SPF 30 Mineral With Antioxidants (titanium dioxide 10% and zinc oxide 8%) packaged in 60 ml/2 fl oz, Vivier Canada Inc. / Mfd. for Vivier Pharma, Vaudereull-Dorion OC Canada, J7V 5V5, Champlain, NY USA 12919, Made in Canada, NDC 67226-2232-6. SKU 10-160-ZZ-80059-R
Where it was distributed
Nationwide within the United States
Questions about this recall
Why was it recalled?
Microbial Contamination of Non-Sterile Product
Which lots are affected?
Lot #: 91771, Exp. Date 09/2025
Where was it sold?
Nationwide within the United States
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.