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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 1,426 - 1,450 of 3,321 matching product recalls.
Product Recall Search
Product Recall Source Type Risk Date Action
FDA Z-2019-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: EH BRONCHOSCOPY, Medline Kit Number/SKU DYNJT3270
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
FDA Z-2010-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207.
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
FDA Z-1992-2026
Medical Device High
May 6, 2026 Recall: Apr 3, 2026
Details
Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1. Model Number (REF): 782116 2. Model Number (REF): 782148. 3. Model Number (REF): 782166.
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
FDA Z-1954-2026
Medical Device High
May 6, 2026 Recall: Apr 14, 2026
Details
Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY
catheter may experience resistance when being advanced over the guidewire
FDA Z-2004-2026
Medical Device High
May 6, 2026 Recall: Apr 2, 2026
Details
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. MAJOR NEURO PACK-LF, Medline Kit Number/SKU DYNJ0578916X; 2. ANGIOGRAPHY PACK, Medline Kit Number/SKU DYNJ51637D; 3. NEURO SEO, Medline Kit Number/SKU DYNJ65650.
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
FDA Z-2015-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
FDA Z-2024-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: DERMATOLOGY SHAVE KIT, Medline Kit SKU SK395
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
FDA Z-2044-2026
Medical Device High
May 6, 2026 Recall: Mar 16, 2026
Details
Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: Universal Central/Art Line Insertion Kit, Medline Kit SKU ART155A
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
FDA Z-2039-2026
Medical Device High
May 6, 2026 Recall: Mar 16, 2026
Details
Philips Achieva 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781278.
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
FDA Z-1953-2026
Medical Device High
May 6, 2026 Recall: Apr 14, 2026
Details
Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLY
catheter may experience resistance when being advanced over the guidewire
FDA Z-2002-2026
Medical Device High
May 6, 2026 Recall: Apr 2, 2026
Details
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: GENERAL KIT, Medline Kit Number/SKU DYNJ905664I
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
FDA Z-2031-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 3 CEM. Part Number: 150450203.
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
FDA Z-1989-2026
Medical Device High
May 6, 2026 Recall: Apr 3, 2026
Details
Medline medical procedure kits, containing Medline Neuro Sponges (961 in total), NEURO,
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
FDA Z-2033-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
FDA Z-2017-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
BD GasPak EZ Campy Pouch System. Catalog Number: 260685. for microbiologic use
BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide levels below specification.
FDA Z-1983-2026
Medical Device High
May 6, 2026 Recall: Apr 7, 2026
Details
epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN): 10736515;
Use of the affected product can result in discrepant low pH and measured Total Carbon Dioxide (mTCO2) results and corresponding calculated values in arterial, venous, and capillary patient samples. An erroneously low pH or mTCO2 reading can lead to inappropriate treatment of nonexistent acidosis (respiratory of metabolic) or missed diagnosis of alkalosis (a true high pH: respiratory or metabolic alkalosis), potentially causing harm through unnecessary interventions with the former or failure to deliver appropriate treatment with the latter.
FDA Z-2005-2026
Medical Device High
May 6, 2026 Recall: Apr 2, 2026
Details
i-STAT EG7+ cartridge; List Number: 03P76-25;
Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26) cartridge lots in the U.S. marketplace may report higher than expected PCO2 and lower than expected pH results due to a manufacturing issue. A falsely high pCO2 together with a falsely low pH makes the blood gas appear as if the patient is in severe respiratory acidosis. If the clinician believes the values are real, it may trigger unnecessary or even harmful interventions such as unnecessary ventilator changes, unnecessary medications, potential harm from overcorrection, or delays in identifying true problems.
FDA Z-1999-2026
Medical Device High
May 6, 2026 Recall: Apr 1, 2026
Details
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. OSC COLEMAN FAT HARVEST KIT, Medline Kit Number/SKU DYNJ32854B; 2. RR-DR. CHHETRI MDL PACK, Medline Kit Number/SKU DYNJ62635B.
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
FDA Z-2018-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
FDA Z-2020-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
FDA Z-1987-2026
Medical Device High
May 6, 2026 Recall: Apr 3, 2026
Details
FDA Z-1984-2026
Medical Device High
May 6, 2026 Recall: Mar 26, 2026
Details
Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY
catheter may experience resistance when being advanced over the guidewire
FDA Z-2003-2026
Medical Device High
May 6, 2026 Recall: Apr 2, 2026
Details
FDA Z-1943-2026
Medical Device High
May 6, 2026 Recall: Mar 12, 2026
Details
Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120. 2. Model Number (REF): 782153.
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
FDA Z-1964-2026
Medical Device High
May 6, 2026 Recall: Apr 14, 2026
Details
Showing 1,426 - 1,450 of 3,321 product recalls

Product Recalls Today

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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

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

USDA FSIS

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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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Prioritize High-Risk Notices

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Latest Product Recalls FAQ

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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.

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

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