Medical Device Recalls Today
Review FDA device recalls and early alerts for equipment, software, monitors, implants, diagnostic tools and patient-use devices.
Medical Device Recall Alerts List
Showing 1,676 - 1,678 of 1,678 matching product recalls.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201, 795231, 795232, 795234 REF: 795117, 795122
Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.
|
FDA
Z-1007-2026
|
Medical Device | High |
Jan 7, 2026
Recall: Jul 14, 2022
|
Details |
|
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
|
FDA
Z-1004-2026
|
Medical Device | High |
Jan 7, 2026
Recall: Nov 19, 2025
|
Details |
|
BVI Leos Laser and Endoscopy System. Model Number: OME6000U.
Manufacturing deviation in which the ferrites specified for the USB cable assembly linking the Nurse Monitor touchscreen to the System Controller were not installed as intended. The omission of the ferrites on the USB communication cable results in non-conformance to the design specifications, which require two ferrites (one at each end of the cable).
|
FDA
Z-1008-2026
|
Medical Device | High |
Jan 7, 2026
Recall: Dec 5, 2025
|
Details |
Search The Device Label
Use the device name, company, product code, UDI, model, catalog number, serial number, lot number, software version or implant card details.
Recall Class And Risk Level
Class I recalls are generally the most serious. Read the FDA notice for patient risk, affected devices, correction/removal steps and clinical action.
What To Check On A Device Label
If the device supports or monitors health, do not stop treatment based only on a search result. Confirm with the official notice and your clinician when needed.
How To Check Medical Device Recalls: FDA Device Safety Alerts And Recall Notices
Match The Exact Medical device
Use each recall result to compare device name, company, product code, model, serial, lot number, UDI and software version. A similar name is not enough; recalls often apply only to specific versions or production ranges.
Read The Recall Hazard
Check the notice for FDA recall class, patient risk, correction, removal and clinical action. This helps you decide whether the item should be stopped immediately or handled through a normal remedy process.
Check Where It Was Sold
Review retailer, online marketplace, state, distribution and purchase-date details when they are available. Some recalls apply only to certain stores or channels.
Follow The Official Remedy
Use the linked official notice for final instructions such as repair, replacement, refund, disposal, software update, stop-use or company contact.
Medical Device Recalls: FDA Device Safety Alerts And Recall Notices FAQ
Short answers for checking whether a specific item is included in this recall category.
How do I know if this medical device is recalled?
Search the product name or brand, then compare model, serial, lot, code, date, retailer and official recall number details on the detail page.
What should I do after finding a matching recall?
Stop using the product if the official notice says to do so, keep the label or packaging, and follow the remedy instructions for repair, refund, replacement or disposal.
Why can two similar products have different recall status?
Recalls can be limited to certain production dates, factories, lots, model numbers, colors, sizes, retailers or distribution areas.
Is this page the official recall notice?
No. This page helps you search public recall data. Use the linked agency or company notice as the final source before taking action.