Class II · Moderate risk
Naturmetic SPF 50 Sunscreen
GMP Deviations
Is Magnolia recalled?
Not under an active recall.
Magnolia was recalled 4 times in the past — all now closed. Most recent: May 4, 2018.
Most common reason: Wrong potency / content (3 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Magnolia. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Magnolia recalls on record
none so far in 2026; 4 on record, newest first
Class II · Moderate risk
Cardec DM Drops
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Class II · Moderate risk
Cardec Drops
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Class II · Moderate risk
Brompheniramine/Pseudoephedrine Dm
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
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