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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 451 - 475 of 4,622 matching product recalls.
Product Recall Search
Product Recall Source Type Risk Date Action
FDA Z-0034-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
FDA Z-3273-2026
Medical Device High
Oct 7, 2026 Recall: Aug 20, 2026
Details
FDA Z-0054-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
FDA Z-0031-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
FDA Z-0030-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
Positron Emission Tomography and Computed Tomography System, Model: uMI 780
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.
FDA Z-3288-2026
Medical Device High
Oct 7, 2026 Recall: Aug 11, 2026
Details
FDA Z-0058-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
FDA Z-0024-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
FDA Z-0047-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
Upgrade to MR 7700; Model number (REF): 782130; Software Versions: R11, R12 and R13;
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.
FDA Z-3317-2026
Medical Device High
Oct 7, 2026 Recall: Aug 28, 2026
Details
FDA Z-0066-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
FDA Z-0042-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
FDA Z-0008-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
FDA Z-0032-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
Intrapulmonary Percussive Ventilation, IPV-1C, Product Number: S00002-C; Phasitron 5, Product Number: P5 used with Instruction Manual
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation
FDA Z-3321-2026
Medical Device High
Oct 7, 2026 Recall: Aug 18, 2026
Details
Brand Name: Opportunity Pro Product Name: Opportunity Pro Model/Catalog Number: 72-50800, 72-50801,72-50802,72-50803,72-50804 Product Description: Blue Nitrile patient examination glove
Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to infectious pathogens leading to infection or cross-contamination, or exposure to chemical agents leading to irritation or systemic toxicities.
FDA Z-3291-2026
Medical Device High
Oct 7, 2026 Recall: Aug 14, 2026
Details
FDA Z-3335-2026
Medical Device High
Oct 7, 2026 Recall: Aug 17, 2026
Details
FDA Z-3270-2026
Medical Device High
Oct 7, 2026 Recall: Jul 27, 2026
Details
FDA Z-0011-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
Positron Emission Tomography and Computed Tomography System, Model: uMI 550 with software
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.
FDA Z-3283-2026
Medical Device High
Oct 7, 2026 Recall: Aug 11, 2026
Details
FDA Z-0061-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
FDA Z-3302-2026
Medical Device High
Oct 7, 2026 Recall: Aug 20, 2026
Details
FDA Z-3304-2026
Medical Device High
Oct 7, 2026 Recall: Aug 20, 2026
Details
Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ROBOTIC PACK - 242561 Model No. MHRB88AO
Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. Use of a contaminated wipe may lead to localized skin effects such as irritation, erythema, or mild inflammation. Failure to perform pericare due to disposal of contaminated wipes may increase risk of localized infection or catheter-associated urinary tract infection (CAUTI).
FDA Z-3292-2026
Medical Device High
Oct 7, 2026 Recall: Aug 10, 2026
Details
Brand Name: Tandem t:slim mobile application Product Name: t:slim Mobile Application, iOS Model/Catalog Number: iOS software version 2.13 Software Version: iOS software version 2.13 UDI-DI: 00389152470740 Component: No
A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a software issue preventing successful pairing of the t:slim application with Abbott FreeStyle Libre 3 Plus (FSL3P) continuous glucose monitoring (CGM) sensors, resulting in the insulin pump being unable to establish a near-field communication (NFC) connection with the CGM and requiring FSL3P users to use their t:slim insulin pumps in manual mode. FSL3P users are unable to access their CGM's glucose values from within the t:slim app and cannot use their pumps in automated control (closed-loop) mode, which could lead to users experiencing hypoglycemia or hyperglycemia.
FDA Z-3330-2026
Medical Device High
Oct 7, 2026 Recall: Jul 16, 2026
Details
Showing 451 - 475 of 4,622 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.

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Check The Publish Date First

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Prioritize High-Risk Notices

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Verify The Official Notice

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Latest Product Recalls FAQ

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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.