RecallRadar

FDA Device recall Z-0280-2023

VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS-IR) Product Number: 174-0012

On 2022-11-30 the FDA classified a Class II recall of VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS-IR) Product Number: 174-0012 by Visionsense, citing broken Optical fiber cable damage can occur through handling or bending and can lead to loss of functionality and heating/melting of the outer cable surface.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0280-2023
ClassificationClass II
Statusongoing
Initiated2022-10-17
Published2022-11-30
Last updated2026-09-13 11:56 UTC
CompanyVisionsense
DistributionUS

Product

VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS-IR) Product Number: 174-0012

Reason

Broken Optical fiber cable damage can occur through handling or bending and can lead to loss of functionality and heating/melting of the outer cable surface.

Identifiers

code_info
UDI-DI: 18130400103489 Lot Numbes: 3784719 3784735 3784751 378-4001 378-4002 378-4003 378-4004 378-4006 378-4007 378-4…UDI-DI: 18130400103489 Lot Numbes: 3784719 3784735 3784751 378-4001 378-4002 378-4003 378-4004 378-4006 378-4007 378-4008 378-4009 378-4010 378-4012 378-4013 378-4014 378-4015 378-4016 378-4017 378-4020 378-4021 378-4501 378-4502 378-4503 378-4504 378-4505 378-4506 378-4507 378-4508 378-4510 378-4511 378-4512 378-4513 378-4515 378-4529 378-4531 378-4535 378-4537 3784581 378-4582 378-4583 378-4584 378-4588 378-4589 378-4590 3784592 378-4593 378-4594 3784595 378-4596 3784599 3784601 378-4602 3784603 378-4604 3784605 3784606 3784609 3784610 3784612 3784613 3784614 3784617 378-4618 3784619 3784620 3784621 3784622 3784623 3784624 3784626 3784627 3784628 3784629 3784632 3784633 3784635 3784636 3784637 3784638 3784641 3784644 3784645 3784646 3784648 3784649 3784650 3784651 3784652 3784653 3784654 3784656 378-4657 378-4658 3784659 3784660 3784661 3784662 3784663 3784664 3784665 3784666 3784667 3784669 3784671 3784672 3784674 378-4675 3784676 378-4677 3784679 3784680 3784681 3784682 3784683 37

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0280-2023%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.