FDA recall record

Accure Laser System, Model: PFMS00004 recall — FDA Z-0778-2024

Laser system's spot tracking system may become misaligned resulting in the possible risk of delivery of higher-than-expected laser energy to epidermal…

Class IIclassification
Z-0778-2024official record ID
Jan 31, 2024report date

Recall record at a glance

Official recordZ-0778-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmAccure Acne, Inc.
Report dateJan 31, 2024
Recall initiation dateDec 6, 2023
Quantity22
LocationBoulder, CO, United States

Official product description

Accure Laser System, Model: PFMS00004

Why the product was recalled

Laser system's spot tracking system may become misaligned resulting in the possible risk of delivery of higher-than-expected laser energy to epidermal tissue, which may cause blistering.

Distribution information

US distribution to states of: CO, CA, CT, NY, NJ, MN, LA, OH, MA, TX

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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