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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 1,401 - 1,425 of 3,321 matching product recalls.
Product Recall Search
Product Recall Source Type Risk Date Action
Allura Imports Recalls Youth Sweatshirts with Bobcat Logo and Drawstrings Due to Risk of Serious Injury or Death from Strangulation Hazard; Violates Federal Regulations for Children's Upper Outerwear
Allura Imports Recalls Youth Sweatshirts with Bobcat Logo and Drawstrings Due to Risk of Serious Injury or Death from Strangulation Hazard; Violates Federal Regulations for Children's Upper Outerwear
This recall involves youth sweatshirts with drawstrings. The sweatshirts are gray and have the Bobcat name and logo printed in black on the chest of the sweatshirt. The sweatshirts were sold in youth sizes 8/10 and 12/14. The size of the sweatshirt and "RN#36753" is printed on the neck label in black.
CPSC 10764
Child/Baby High
May 7, 2026 Recall: May 7, 2026
Details
FDA H-0686-2026
Food High
May 6, 2026 Recall: Apr 2, 2026
Details
FDA H-0683-2026
Food High
May 6, 2026 Recall: Feb 14, 2026
Details
FDA H-0685-2026
Food High
May 6, 2026 Recall: Apr 23, 2026
Details
FDA H-0684-2026
Food High
May 6, 2026 Recall: Apr 20, 2026
Details
FDA H-0676-2026
Food High
May 6, 2026 Recall: Apr 13, 2026
Details
FDA H-0675-2026
Food High
May 6, 2026 Recall: Mar 26, 2026
Details
FDA H-0680-2026
Food High
May 6, 2026 Recall: Apr 14, 2026
Details
FDA H-0678-2026
Food High
May 6, 2026 Recall: Apr 13, 2026
Details
FDA H-0677-2026
Food High
May 6, 2026 Recall: Apr 13, 2026
Details
Negita Cracker- Shrimp 2.8oz
Contains undeclared FD&C Yellow 6
FDA H-0679-2026
Food High
May 6, 2026 Recall: Apr 16, 2026
Details
Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781260. 2. Model Number (REF): 782112.
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-1965-2026
Medical Device High
May 6, 2026 Recall: Apr 14, 2026
Details
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Part Number: 150450204.
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
FDA Z-1990-2026
Medical Device High
May 6, 2026 Recall: Apr 3, 2026
Details
Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781270. 2. Model Number (REF): 782113.
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-1967-2026
Medical Device High
May 6, 2026 Recall: Apr 14, 2026
Details
Medline and Centurion medical procedure kits, containing Medline Neuro Sponges (1229 in total), HEAD & NECK TRAY, SINUS, SMR, etc.
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-2021-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF): 781356. 2. Model Number (REF): 782109. 3. Model Number (REF): 782138. 4. Model Number (REF): 782160.
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-1961-2026
Medical Device High
May 6, 2026 Recall: Apr 14, 2026
Details
Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782130.
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-1969-2026
Medical Device High
May 6, 2026 Recall: Apr 14, 2026
Details
FDA Z-2036-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
Medline medical procedure kits, containing Medline Neuro Sponges (102 in total)
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-2025-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number: 00-5049-011-00 Software Version: N/A Product Description: Mixing Bowl and Spatula Component: N/A
Ten complaints have been received identifying issues at the time of use related to the package seal, including incomplete seals, wrinkles in the seals or peeling seals. Compromised sterile barrier may lead to clinically insignificant extension of surgery or infection leading to surgical intervention.
FDA Z-1946-2026
Medical Device High
May 6, 2026 Recall: Mar 30, 2026
Details
FDA Z-1945-2026
Medical Device High
May 6, 2026 Recall: Mar 9, 2026
Details
Centurion medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SURGICAL ENT PREP KIT, Medline Kit Number/SKU MNS11715
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-2028-2026
Medical Device High
May 6, 2026 Recall: Mar 19, 2026
Details
Philips Ingenia Elition S with MR Elastography (MRE). 1. Model Number (REF): 781357. 2. Model Number (REF): 782106. 3. Model Number (REF): 782137.
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-1962-2026
Medical Device High
May 6, 2026 Recall: Apr 14, 2026
Details
i-STAT EG6+ cartridge; List Number: 03P77-25;
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-2000-2026
Medical Device High
May 6, 2026 Recall: Apr 1, 2026
Details
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 4 CEM. Part Number: 150450104.
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
FDA Z-1985-2026
Medical Device High
May 6, 2026 Recall: Apr 3, 2026
Details
Showing 1,401 - 1,425 of 3,321 product recalls

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CPSC

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FDA

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Latest Product Recalls FAQ

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