How many FDA warning letters has Jolife AB received?

Argus HQ has not recorded an FDA warning letter for Jolife AB in our current dataset.

What FDA recalls has Jolife AB issued?

Argus HQ has recorded 1 FDA recall tied to Jolife AB.

Is Jolife AB FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for Jolife AB. Review the linked FDA source records directly before drawing a compliance conclusion.

.hq

company

Jolife AB

Name: FDA Enforcement Actions Against Jolife AB
Creator: Argus HQ
License: https://argushq.ai/methodology

Jurisdiction: US

FDA Warning Letter timeline

V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.

fda_recall · device_recall2026-05-20
Jolife AB — Class II recall: LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UD…

Frequently asked questions

How many FDA warning letters has Jolife AB received?: Argus HQ has not recorded an FDA warning letter for Jolife AB in our current dataset.
What FDA recalls has Jolife AB issued?: Argus HQ has recorded 1 FDA recall tied to Jolife AB.
Is Jolife AB FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for Jolife AB. Review the linked FDA source records directly before drawing a compliance conclusion.

Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.