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Recall Observatory FDA recall evidence

Device product

Accure Laser System, Model: PFMS00004

Z-0778-2024

December 06, 2023

Class II

Product summary

Firm
Accure Acne, Inc
Event
Event 93696
Status
Ongoing
Classification
Class II
Quantity
22
Official record key
device-enforcement:Z-0778-2024

Official wording

Reason: 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.

Code information: UDI-DI: 08059173392230, Serial Numbers: LAD0000-0004, LAD0000-0014, PROT01-0720, LAD0000-0012, LAD0000-0005, LAD2216-0623, LAD2356-0723, LAD0000-0003, PROTO07-1120, LAD2076-0623, LAD0000-0011, LAD0000-0008, LAD0000-0010, LAD2357-0723, LAD2075-0623, LAD2232-0723, LAD0000-0013, LAD0000-0009, LAD0000-0006, LAD0000-0001, PROT06-1120, LAD2507-0723

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.