Allura Xper FD10/10; Model Number: 722027; Recall Details
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
Medical DeviceHigh riskJan 21, 2026
Confirm With The Official Notice
Use this page to screen for a possible match. Use the linked official notice before you stop use, throw away, return, repair or schedule service.
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
Before you act: a similar product name is not enough. Match the identifiers, affected dates, model or lot details, and remedy instructions in the official notice.
1. Match the item
Check device name, UDI, model, lot, serial and software version.
2. Read the risk
Review the hazard, consequence, risk level and whether the notice says to stop using, stop eating or keep the item away from children.
3. Follow the remedy
Look for refund, repair, replacement, disposal, software update, dealer service or company contact instructions.
4. Verify officially
Open the official source before making a safety decision, especially for vehicles, food, baby products and medical devices.
How To Tell If Yours Is Included
Device recalls can depend on UDI, model, catalog number, lot, serial number, software version or implant card details. Match the label before changing device use.
Recall Hazard And Risk
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
Recall Remedy
Use the official notice for remedy instructions. Product recall remedies may include repair, replacement, refund, disposal, software update, dealer service or a stop-use instruction.
Affected Product Or Item
Allura Xper FD10/10; Model Number: 722027;
Hazard Or Reason For Recall
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
How To Check If This Recall Applies To You
Match The Device Label
Compare UDI, product code, model, catalog number, lot, serial number and software version before changing device use.
Compare Codes And Date Ranges
Check UPCs, lot codes, serial numbers, model numbers, best-by dates, date codes, VIN ranges, production dates or official campaign numbers when available.
Read The Hazard Before Use
Hazards can involve injury, fire, choking, contamination, undeclared allergens, crash risk, device failure, electrical shock or incorrect labeling.
Follow The Official Remedy
Confirm final instructions in the linked official notice before returning, repairing, disposing, stopping use, stopping consumption, contacting the company or scheduling service.
Key Medical Device Recall Checks
Use these checks to decide whether the notice is relevant to the item you have, then confirm with the official source.
Identity
UDI, Model, Lot And Serial
Medical device recalls can depend on UDI, product code, software version, model, lot or serial number.
Risk
Hazard, Consequence And Risk Level
Use the hazard, consequence and risk level to understand whether the product should be stopped immediately or handled through normal recall instructions.
Action
Repair, Replacement, Refund Or Disposal
Recall remedies differ by agency and product type. The official notice is the final source for repair, refund, replacement, disposal, dealer service or stop-use steps.
Source
Official Agency Notice
This page helps you review public recall details in one place. Always use the linked agency or company notice before making a safety decision.
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Short answers for checking whether this recall notice applies to your item.
How do I know if this recall affects my product?
Compare the product name, brand, model, UPC, lot code, serial number, VIN, date code, package size, retailer and distribution details with the official notice. All key details should match.
What should I do after finding a matching recall?
Stop using, feeding, driving or consuming the product when the notice says to do so, then follow the official remedy for repair, replacement, refund, disposal, service or company contact.
Is this page the official recall notice?
No. This site helps you review public recall details. Use the linked official notice as the final source for affected products and safety instructions.
Why can a recall page change after publication?
Agencies and companies may update notices with expanded products, corrected codes, new risk classifications, remedy availability or additional distribution details.