In Your Face tinted mineral sunscreen recalled over manufacturing practice deviations
In Your Face Mineral Tint SPF 31 tinted sunscreen is being recalled because of cGMP deviations. 76 bottles are affected.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class II recall for manufacturing practice deviations with no contamination, potency failure or health consequence stated in the source.
Plain-English summary
In Your Face Mineral Tint SPF 31, zinc oxide 25%, tinted sunscreen broad spectrum UVA & UVB, 50 mL (1.7 fl oz) per bottle, manufactured for In Your Face Skin Care, is being recalled. The action covers 76 bottles.
The stated reason is cGMP deviations, meaning departures from current good manufacturing practice. The FDA classified the action as Class II. The source does not describe a resulting health consequence.
The affected lot is 408-002. Distribution was in New Jersey, Florida and Michigan.
Consumers who have the affected lot should stop using it and follow the instructions issued by the firm.
The recalled product
- Product
- In Your Face Mineral Tint SPF 31, Zinc Oxide 25%, Tinted Sunscreen Broad Spectrum UVA & UVB chemical free, Organic Ingredients, Biodegradable & Baby Safe, 50 mL - 1.7 fl oz per bottle, Manufactured for IN YOUR FACE Skin Care, Belleair Bluffs, FL, Made in USA, NDC: 73369-1601-1
- Manufacturer
- KABANA SKIN CARE
- Category
- Drug — Sunscreen
- Affected units
- 76
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot: 408-002
Distribution
Part of a larger recall action
This product is one of 4 recalled by KABANA SKIN CARE under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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