GreenScreen zinc oxide sunscreen recalled over manufacturing practice deviations
GreenScreen organic zinc oxide sunscreen SPF 32 is being recalled because of cGMP deviations. 174 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
GreenScreen by Kabana Organic Skincare, Broad Spectrum UVA & UVB Zinc Oxide Sunscreen, fragrance free, Original, SPF 32, is being recalled. The action covers 174 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 405-002 and 405-003. 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
- GreenScreen, kabana organic skincare, Bread Spectrum UVA & UVB, Zinc Oxide Sunscreen, Organic Ingredients, Fragrance Free, Biodegradable, Chemical Free, Non-Nano, Baby Safe, Original, SPF 32, Totally Green personal care, Zinc Oxide USP 25%, 3.4 FL OZ/115 G Tube, NDC: 73369-0001-1
- Manufacturer
- KABANA SKIN CARE
- Category
- Drug — Sunscreen
- Affected units
- 174
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)
- Lots: 405-002 and 405-003
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.
See all 4 products in this recall →Related recalls
Same manufacturer · KABANA SKIN CARE
See all →- ModerateIn Your Face tinted mineral sunscreen recalled over manufacturing practice deviations
FDA (Drugs) · 2025-07-16
- ModerateB Natural Organics mineral sunscreens recalled over manufacturing practice deviations
FDA (Drugs) · 2025-07-16
- ModerateErin's Faces mineral sunscreen recalled over manufacturing practice deviations
FDA (Drugs) · 2025-07-16
Same hazard · cgmp deviation
See all →- SevereBaxter Recalls Daptomycin Injection Due to Manufacturing Deviations
FDA (Drugs) · 2026-09-09
- ModerateLexia LLC Recalls Broadway Joe's Pain Cream Due to CGMP Deviations
FDA (Drugs) · 2026-09-09
- SevereBaxter Recalls Daptomycin Injection Due to Manufacturing Deviations
FDA (Drugs) · 2026-09-09
- HighBaxter Recalls Clindamycin Injection Due to Manufacturing Deviations
FDA (Drugs) · 2026-09-09
- SevereBaxter Recalls Clindamycin Injection Due to Manufacturing Deviations
FDA (Drugs) · 2026-09-09