B Natural Organics mineral sunscreens recalled over manufacturing practice deviations
B Natural Organics Organic Sunscreen SPF 30, in tinted and tint free formulas, is being recalled because of cGMP deviations. 204 tubes are affected.
What this means for you
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
B Natural Organics, Organic Sunscreen, Broad Spectrum, SPF 30, 25% non-nano zinc oxide, in the Nude Tint Mineral Formula for Face and Body (4 oz, NDC 73369-1002-2) and the Tint Free Mineral Formula for Face and Body, is being recalled. The action covers 204 tubes.
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.
Affected lots are 410-001 expiring 10/31/2027, 404-003 expiring 04/30/2027 and 404-001 expiring 04/30/2027. Distribution was in New Jersey, Florida and Michigan.
Consumers who have an affected lot should stop using it and follow the instructions issued by the firm.
The recalled product
- Product
- B Natural Organics, Organic Sunscreen, Broad Spectrum, SPF 30, 25% non-nano Zinc Oxide, a) Nude Tint Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1002-2; b) Tint Free Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1001-2; c)
- Manufacturer
- KABANA SKIN CARE
- Category
- Drug — Sunscreen
- Affected units
- 204
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 (4)
- Lots: a) 410-001
- Exp 10/31/2027 b) 404-003
- Exp 04/30/2027 c) 404-001
- Exp 04/30/2027
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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