Nasalprodukter Sverige AB
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
Devices registered here (1)
- Catheters, Suction, TracheobronchialProduct code BSY (opens in a new tab) · Class I · Anesthesiology · 21 CFR 868.6810
Recalls & enforcement
- Class IIOngoing2020-01-27FridaBaby has been made aware through customer reports that the product is being used outside of the labeled directions. Specifically, repeated chewing or biting on the SmileFrida, the ToothHugger has caused deterioration in the outer layer of the brush and in very rare occasion…
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Nasalprodukter Sverige AB (FEI 3005833605) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3005833605-nasalprodukter-sverige-ab/
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