Product Recalls Today
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
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.
Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
Huish Outdoors Recalls Hollis Diving Regulators Due to Risk of Serious Injury or Death from Drowning
This recall involves Hollis 200LX second stage diving regulators. The regulators are used for Scuba diving and are made of black and red plastic and metal. "200LX" and "Hollis" are engraved on top of the regulator. The product serial number is located under the mouthpiece. The following serial number ranges are included in this recall: Serial Number Ranges C3753 - C77735 S73202 - S8442 HA00001 - HA14873 LX001698 - LX009896
|
CPSC
10867
|
Consumer Product | High |
Jul 17, 2026
Recall: Jul 16, 2026
|
Details |
Currey & Company Recalls Nottaway Chandeliers Due to Risk of Serious Injury or Death from Electrocution Hazard
This recall involves Currey & Company's Nottaway chandeliers. The iron with brass frame light fixtures were sold in gold, bronze and champagne finishes and in two sizes. The two-tier chandeliers measure about 44 inches in diameter and 44.5 inches high and have an adjustable drop of 51 to 119 inches and nine 50-watt bulbs. The three-tier chandeliers measure about 60 inches in diameter and 63.5 inches high and have an adjustable drop of 70 to 138 inches and 18 40-watt bulbs. "Currey & Company" and the model number 9000-1129, 9000-1130, 9000-1254, 9000-1255, 9000-1314 are printed on a label atop the fixture's ceiling canopy. Nottaway and the model are printed on the product order receipt. Only chandeliers with no visible screw on the outside of the top distributor cap are included in this recall.
|
CPSC
10864
|
Consumer Product | High |
Jul 17, 2026
Recall: Jul 16, 2026
|
Details |
|
Steel Wheels May Crack and Separate
Chrysler (FCA US, LLC) is recalling certain 2026 Jeep Gladiator and Jeep Wrangler vehicles. The walls for the steel wheels may be too thin, allowing them to crack or detach, which can result in a loss of vehicle control. Loss of vehicle control increases the risk of a crash.
|
NHTSA
26V456000
|
Vehicle | High |
Jul 16, 2026
Recall: Jul 16, 2026
|
Details |
|
Water May Damage Rearview Camera
Jaguar Land Rover North America, LLC (Land Rover) is recalling certain 2021-2025 Land Rover Discovery vehicles. Water may not be able to drain away from the rearview camera due to insufficient drain holes, which may result in damage to the rearview camera. A rearview camera image that does not display can decrease the driver's visibility, increasing the risk of a crash.
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NHTSA
26V458000
|
Vehicle | High |
Jul 16, 2026
Recall: Jul 16, 2026
|
Details |
|
Body Panel Joints Incorrectly Attached/FMVSS 221
International Motors, LLC (International) is recalling certain 2025-2027 IC Bus EVSB and CESB school buses. The driver's window panel and entrance door vertical joints may have been attached without sufficient epoxy coverage. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) No. 221, "School Bus Body Joint Strength." The body panels may separate during a crash, reducing structural integrity and increasing the risk of injury.
|
NHTSA
26V460000
|
Vehicle | High |
Jul 16, 2026
Recall: Jul 16, 2026
|
Details |
|
FDA
H-1142-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details | |
|
Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is refrigerated. UPC 1 00000 01030 3. Manufactured by LPK1 Renton, WA. Product was not sold at retail stores and sold only to employees at certain business' breakroom.
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.
|
FDA
H-1148-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 25, 2026
|
Details |
|
High Valley Orchard Chocolate Covered Raisins, net wt. 15oz. per package, each case contains 12/15oz. bags. Product is packaged in clear plastic container. UPC on retail container: 0 952348 80170 0. The label of affected product declares: INGREDIENTS: MILK CHOCOLATE (SUGAR, ***WHOLE MILK POWDER, SOY LECITHIN ***RAISINS***CONTAINS MILK AND SOY*** Distributed by Lehi Valley Trading Company of Mesa, AZ.
Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packaging.
|
FDA
H-1150-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 24, 2026
|
Details |
|
JB Chicken Sknls 35.73#
Undeclared Sesame allergen
|
FDA
H-1139-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details |
|
Alabama Banana Pudding Marshmallow, 4 ounce 16 pieces of individual marshmallows packaged in a sealed plastic bag inside a printed cardboard box
Foreign material: small metal pieces
|
FDA
H-1147-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 11, 2026
|
Details |
|
Fresh to You Burger Chicken Fillet, SKU 10150, Net wt. 5oz. Product is refrigerated. UPC 1 00000 01015 0. Manufactured By LPK1 Renton, WA. Product was not sold at retail stores and sold only to employees at certain business' breakroom.
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Fillet sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.
|
FDA
H-1149-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 25, 2026
|
Details |
|
Coopers Bbq 60 Gal Bean Mix box
Undeclared Sesame allergen
|
FDA
H-1141-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details |
|
FDA
H-1145-2026
|
Food | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details | |
|
Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER; NET WEIGHT: 15 KGS; packaged in brown paper bags with a white label
Potential contamination with Salmonella
|
FDA
H-1144-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 24, 2026
|
Details |
|
Wise Onion Rings, 3.75 oz, metalized film in cardboard cartons, 14 bags per case,
The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.
|
FDA
H-1146-2026
|
Food | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details |
|
EC Hot Links Seasoning 45.05#
Undeclared Sesame allergen
|
FDA
H-1140-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details |
|
FDA
H-1143-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 24, 2026
|
Details | |
|
Smoked Sausage Spice 32.86#
Undeclared Sesame allergen
|
FDA
H-1138-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details |
|
OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.
The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110 minutes, or 120 minutes depending on the sterilization cycle exposure time used.
|
FDA
Z-2714-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 5, 2026
|
Details |
|
Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569D; 2) ACCESSORY KIT, Model Number: DYNJ901348F
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.
|
FDA
Z-2696-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details |
|
Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 341-14-711 Product Description: Enovis knee devices are for knee arthroplasty.
Due to packaging discrepancy with incorrect product size mixed up.
|
FDA
Z-2701-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Feb 16, 2026
|
Details |
|
Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 342-19-703 Product Description: Enovis knee devices are intended for knee arthroplasty.
Due to packaging discrepancy with incorrect product size mixed up.
|
FDA
Z-2700-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Feb 16, 2026
|
Details |
|
Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DYNJ88569A; 3) OPEN HEART PEDS PACK, Model Number: DYNJ88569B; 4) OPEN HEART PEDS PACK, Model Number: DYNJ88569C
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.
|
FDA
Z-2697-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details |
|
Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS INSTRUMENTS- DRILL EU/RLV0035-EU, INTRACEPT ACCESS INSTRUMENTS- 2VB/RLV0045, INTRACEPT ACCESS INSTRUMENTS- 2VB EU/RLV0045-EU, INTRACEPT ACCESS INSTRUMENTS- 3VB/RLV0055, INTRACEPT ACCESS INSTRUMENTS- 3VB EU/RLV0055-EU, INTRACEPT ACCESS INSTRUMENTS 2 VB/RLV0065, INTRACEPT ACCESS INSTRMNTS ADDITIONAL VB/RLV0075, INTRACEPT ACCESS INSTRMNTS ADDTL VB EU/RLV0075-EU
Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if breached could lead to severe infection.
|
FDA
Z-2694-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Apr 22, 2026
|
Details |
|
VITEK 2 AST-N447 TEST KIT Product reference 424620
Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.
|
FDA
Z-2715-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 4, 2026
|
Details |
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Recent recalls can include new notices, updated classifications, expanded lots, changed risk levels and public health alerts. Sort by newest first for the live recall feed view.
High-risk notices often involve serious injury, contamination, undeclared allergens, vehicle crash hazards, fire risks or products that should not be used or consumed.
This latest recall page combines CPSC, FDA, USDA FSIS and NHTSA data so shoppers do not need to check each agency page separately.
New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.
FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.
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Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.
Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.
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.
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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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