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Latest Product Recalls Today

Track recent product recall alerts from official U.S. sources. Filter by recall date, source agency, risk level and product category to find newly published food, vehicle, baby product, medical device and consumer product recalls.

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Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.

Recent Product Recall Alerts List

Showing 1,876 - 1,900 of 3,321 matching product recalls.
Product Recall Search
Product Recall Source Type Risk Date Action
Allura Xper FD10C; System Code: 722001;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA Z-1659-2026
Medical Device High
Apr 8, 2026 Recall: Mar 3, 2026
Details
MEDLINE ANTERIOR HIP PACK DYNJ64672B
Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
FDA Z-1711-2026
Medical Device High
Apr 8, 2026 Recall: Feb 16, 2026
Details
MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851)
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
FDA Z-1744-2026
Medical Device High
Apr 8, 2026 Recall: Feb 13, 2026
Details
FDA Z-1654-2026
Medical Device High
Apr 8, 2026 Recall: Jan 29, 2026
Details
Vue Motion V12. Product Number: 1017979.
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
FDA Z-1692-2026
Medical Device High
Apr 8, 2026 Recall: Mar 5, 2026
Details
Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA Z-1678-2026
Medical Device High
Apr 8, 2026 Recall: Mar 3, 2026
Details
ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA Z-1663-2026
Medical Device High
Apr 8, 2026 Recall: Mar 3, 2026
Details
Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage.
Potential for attenuation degradation over time, decreasing the lifespan.
FDA Z-1758-2026
Medical Device High
Apr 8, 2026 Recall: Feb 11, 2026
Details
FDA Z-1700-2026
Medical Device High
Apr 8, 2026 Recall: Dec 9, 2025
Details
Burlington Medical, Kilt
Potential for attenuation degradation over time, decreasing the lifespan.
FDA Z-1755-2026
Medical Device High
Apr 8, 2026 Recall: Feb 11, 2026
Details
Allura Xper FD20/20; System Code: 722038;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA Z-1669-2026
Medical Device High
Apr 8, 2026 Recall: Mar 3, 2026
Details
Allura Xper FD20/15; System Code: 722058;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA Z-1671-2026
Medical Device High
Apr 8, 2026 Recall: Mar 3, 2026
Details
Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
FDA Z-1646-2026
Medical Device High
Apr 8, 2026 Recall: Mar 2, 2026
Details
Burlington Medical, Caps.
Potential for attenuation degradation over time, decreasing the lifespan.
FDA Z-1760-2026
Medical Device High
Apr 8, 2026 Recall: Feb 11, 2026
Details
Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915
Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
FDA Z-1708-2026
Medical Device High
Apr 8, 2026 Recall: Feb 16, 2026
Details
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Surgical light assembly may not adequate support the weight of the ceiling cover.
FDA Z-1688-2026
Medical Device High
Apr 8, 2026 Recall: Feb 23, 2026
Details
ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA Z-1667-2026
Medical Device High
Apr 8, 2026 Recall: Mar 3, 2026
Details
Burlington Medical, Thyroid Shield.
Potential for attenuation degradation over time, decreasing the lifespan.
FDA Z-1753-2026
Medical Device High
Apr 8, 2026 Recall: Feb 11, 2026
Details
eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
FDA Z-1731-2026
Medical Device High
Apr 8, 2026 Recall: Mar 2, 2026
Details
ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA Z-1662-2026
Medical Device High
Apr 8, 2026 Recall: Mar 3, 2026
Details
MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
FDA Z-1742-2026
Medical Device High
Apr 8, 2026 Recall: Feb 13, 2026
Details
FDA Z-1697-2026
Medical Device High
Apr 8, 2026 Recall: Dec 9, 2025
Details
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
FDA Z-1693-2026
Medical Device High
Apr 8, 2026 Recall: Feb 18, 2026
Details
FDA Z-1704-2026
Medical Device High
Apr 8, 2026 Recall: Jul 21, 2025
Details
Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL-SLS Model/Catalog Number: TFL-SLS containing TFL-CSLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate soft tissue with moderate hemostasis, little charring, and a thin zone of necrosis. Component: No
Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperable. Additionally, smoke or a burning smell may occur. By design, the issue causing the smoke or burning smell would be contained within the internal laser console enclosure and would be self-extinguishing.
FDA Z-1695-2026
Medical Device High
Apr 8, 2026 Recall: Feb 27, 2026
Details
Showing 1,876 - 1,900 of 3,321 product recalls

Product Recalls Today

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Recent Product Recall Alerts

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High-Risk Recall Updates

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Daily Official Source Coverage

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Latest Recalls By Source Agency

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CPSC

Latest Consumer Product Recalls

New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.

FDA

Latest Food And Medical Device Recalls

Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.

USDA FSIS

Latest Meat And Poultry Recall Alerts

FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.

NHTSA

Latest Vehicle Recall Campaigns

New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.

How To Use The Latest Product Recalls Page

Check The Publish Date First

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Filter By Product Type

Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.

Prioritize High-Risk Notices

Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.

Verify The Official Notice

Use the detail page and official source link before taking action. Agency notices may include exact lot codes, model ranges, remedy steps and company contacts.

Latest Product Recalls FAQ

Helpful context for searches such as product recalls today, recent product recalls and recall alerts.

How often is the latest product recall list updated?

The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.

Why do some recent recalls have older recall dates?

Some agencies publish or classify a recall after the company began the recall. Use both the published date and recall date when reviewing a notice.

What should I check on a recent food recall?

Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.

Can I get only high-risk recalls?

Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.