ACON Laboratories Inc.
1 recall(s) on record — most severe on record: Class III.
Recalls by year
- Recalls (1)
Registered facilities (2)
- ACON BIOTECH (HANGZHOU) CO., LTD. FEI 3002829675 · CN
- Acon Biotech (Hangzhou) Co., Ltd. FEI 3032171519 · CN
Recalls & enforcement
- Class IIITerminated2015-06-17Acon Laboratories, Inc. is recalling Mission Breath Alcohol Detector due to a labeling amendment.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “ACON Laboratories Inc. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9033096-acon-laboratories-inc/
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