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 |
|---|---|---|---|---|---|
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Disconnected Half-Shaft May Cause Loss of Drive Power
Lucid USA, Inc. (Lucid) is recalling certain 2024-2026 Air vehicles equipped with Pure Rear-Wheel Drive. Improperly secured bolts may allow the half-shaft to disconnect from the drive unit. A disconnected half shaft can result in a loss of drive power, increasing the risk of a crash.
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NHTSA
26V193000
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Vehicle | High |
Mar 26, 2026
Recall: Mar 26, 2026
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Details |
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Fuel Hose May Disconnect and Leak Fuel
Honda (American Honda Motor Co.) is recalling certain 2025 CB1000SP motorcycles. The fuel feed hose may disconnect from the fuel tank, causing a fuel leak. A fuel leak near the rear tire can increase the risk of a crash or injury. In addition, a fuel leak in the presence of an ignition source increases the risk of a fire.
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NHTSA
26V194000
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Vehicle | High |
Mar 26, 2026
Recall: Mar 26, 2026
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Details |
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FSIS Issues Public Health Alert for Beef and Pork Products Produced Without the Benefit of Inspection
Editor’s Note: Mar. 30, 2026 – The labels in this release were revised to remove unrelated product that was inadvertently included in the background of some photos. WASHINGTON, March 25, 2026 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for various raw beef and pork products that were produced without the benefit of federal inspection and may bear a false mark of inspection. Food produced without inspection may contain undeclared allergens, harmful bacteria, or other contaminants that put consumer health and safety at risk. FSIS is continuing to investigate and may add additional products to this alert as more information is obtained. The beef and pork items were produced from April 2024 through March 2026. The following products subject to the public health alert are [ view labels ]: 5-lb. box of 8-oz. packages containing a VACUUM-PACKED piece of "BLACKWING ORGANIC MEATS ORGANIC BEEF NEW YORK STRIP STEAK," with "EST. 1996" inside the USDA mark of inspection. 10-lb. box of 16-oz. packages containing a VACUUM-PACKED package of "BLACKWING ORGANIC MEATS ORGANIC GROUND BEEF." 5-lb. box of 8-oz. packages containing a VACUUM-PACKED package of "BLACKWING ORGANIC MEATS GRASS FED ORGANIC BEEF STEW MEAT," with "EST. 1996" inside the USDA mark of inspection. 5-lb. box of 8-oz. packages containing a VACUUM-PACKED piece of "BLACKWING ORGANIC MEATS ORGANIC BEEF STEAK STRIPS," with "EST. 1996" inside the USDA mark of inspection. 1-lb. VACUUM-PACKED package of "BLACKWING MEATS BLACKWING BEEF GROUND FROM ORGANIC BEEF," without USDA mark of inspection. 12-oz. VACUUM-PACKED package of "BLACKWING MEATS PORK GROUND MADE FROM ORGANIC PORK," without USDA mark of inspection. 12-oz. VACUUM-PACKED package of "BLACKWING MEATS Boneless Center Cut Pork Chops 2-6oz Made from Organic Pork," without the USDA mark of inspection. The first four products include the unauthorized use of establishment number "EST. 1996" inside a false USDA mark of inspection. These items were shipped to wholesale and retail locations nationwide. The problem was discovered as part of an ongoing FSIS investigation. There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a health care provider. FSIS is concerned that some product may be in retailer or consumer freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. Media and consumers with questions regarding the public health alert can contact Roger Gerber, Blackwing Meats, President, at 847-838-4888 or [email protected] . Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to [email protected] . For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/ .
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FSIS
PHA-03252026-01
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Food | Medium |
Mar 25, 2026
Recall: Mar 25, 2026
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Details |
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Convatec, EsteemBody Drainable Pouch REF:423657 10-35mm
Drainable large pouch may leak due to manufacturing issue.
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FDA
Z-1584-2026
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Medical Device | High |
Mar 25, 2026
Recall: Feb 16, 2026
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Details |
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Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 5826659-027, 5826659-029, 5826659-032, 5826659-033, 5826659-028, 5826659-034, 5826659-030, 5826659-019, 5826659-022, 5826659-026, 5826659-023, 5826659-031, 5826659-025, 5826659-002, 5826659-021, 5826659-037, 5826659-014, 5826659-016, 5826659-013
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
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FDA
Z-1569-2026
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Medical Device | High |
Mar 25, 2026
Recall: Jan 30, 2026
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Details |
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Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version 3.2.0.1 Product Description: Welch Allyn Spot Vision Screener VS100, FDA product code name: Refractometer, ophthalmic One unit per package
Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.
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FDA
Z-1573-2026
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Medical Device | High |
Mar 25, 2026
Recall: Feb 18, 2026
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Details |
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Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applicable Product Description: Influenza A/B virus nucleic acid IVD, kit, nucleic acid technique Component: Not Applicable
It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.
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FDA
Z-1565-2026
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Medical Device | High |
Mar 25, 2026
Recall: Feb 9, 2026
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Details |
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Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-026, 2088026-115, 2088026-043, K2042VJED, 2088026-132, 2088026-003, 2088026-110, 2089629-003, 2066908-136, 2066908-150
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
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FDA
Z-1571-2026
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Medical Device | High |
Mar 25, 2026
Recall: Jan 30, 2026
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Details |
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Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product Description: Aptima HPV assay Component: No
Due to product exhibiting potential to generate either invalid or false negative results.
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FDA
Z-1586-2026
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Medical Device | High |
Mar 25, 2026
Recall: Feb 18, 2026
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Details |
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Cub Pediatric Crib, Model FL19H
Cribs sold in the USA are missing two access door warning labels.
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FDA
Z-1580-2026
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Medical Device | High |
Mar 25, 2026
Recall: Feb 18, 2026
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Details |
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Artegraft Vascular Graft; REF#: AG740;
Labeling mix-up resulting in the incorrect lot outer packaging of product.
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FDA
Z-1574-2026
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Medical Device | High |
Mar 25, 2026
Recall: Feb 10, 2026
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Details |
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Convatec, EsteemBody Drainable Pouch REF:423653 10-35mm
Drainable large pouch may leak due to manufacturing issue.
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FDA
Z-1583-2026
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Medical Device | High |
Mar 25, 2026
Recall: Feb 16, 2026
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Details |
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Convatec, EsteemBody Drainable Pouch REF:423643, 10-45mm
Drainable large pouch may leak due to manufacturing issue.
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FDA
Z-1582-2026
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Medical Device | High |
Mar 25, 2026
Recall: Feb 16, 2026
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Details |
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Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF 00515 Product Description: The STA¿ - Liatest ¿ D-Di kit is an immuno-turbidimetric assay for the quantitative determination of D-dimer in venous plasma (in 3.2 % sodium citrate) for use on STA-R¿, STA Compact¿ and STA Satellite¿ analyzers by professional laboratory personnel. The STA¿ - Liatest¿ D-Di is intended for use in conjunction with a clinical pretest probability (PTP) assessment model to exclude pulmonary embolism (PE) and deep venous thrombosis (DVT) in outpatients suspected of PE or DVT. Component:
After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.
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FDA
Z-1585-2026
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Medical Device | High |
Mar 25, 2026
Recall: Feb 5, 2026
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Details |
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Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406, 2100169-001, 2088026-985, 2088026-971, 2088026-614, 2088026-713, 2088026-994, 2100491-006, 2088026-723, 2088026-308, 2104867-044, 2100491-012, 2088026-962, 2088026-969, 2102676-001, 2088026-936, 2088026-960, K1220JWED, 2088026-806, 2088026-506, 2088026-026, 2088026-970, 2088026-943, 2088026-990, 2088026-940, 2088026-959, 2088026-967, 2088026-989, 2104867-045, 2088026-993, 2088026-306, 2102675-010,
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
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FDA
Z-1570-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Jan 30, 2026
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Details |
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Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell Gamma Knife¿ Elekta Esprit Leksell Gamma Knife¿ (available models Elekta Esprit, Icon", and Perfexion") is a radiosurgery system for use in the stereotactic irradiation of head structures. Surgery is achieved by delivering a prescribed dose as one or more shots of ionizing radiation to the exact site of the target.
Due to adapter not being properly aligned or locked in place.
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FDA
Z-1581-2026
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Medical Device | High |
Mar 25, 2026
Recall: Feb 18, 2026
|
Details |
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MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.
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FDA
Z-1572-2026
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Medical Device | High |
Mar 25, 2026
Recall: Feb 2, 2026
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Details |
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Battery Charging Station; Model: 0998-00-0802;
The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to operate the IABP. Getinge has identified that a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging. The right bay of the Battery Charging Station is not affected by this issue.
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FDA
Z-1587-2026
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Medical Device | High |
Mar 25, 2026
Recall: Feb 6, 2026
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Details |
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TETAS Mireya, Cherry Milkshake (Colita con Leche), i unit Popsicle, Net wt 6OZ. 170GRS. KEEP FROZEN. UPC Code 83822654822
Undeclared allergen: Soy Lecithin
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FDA
H-0584-2026
|
Food | High |
Mar 25, 2026
Recall: Mar 11, 2026
|
Details |
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Wawa Cookies & Cream Milk 16 oz (Pint), Plastic bottle Store Refrigerated
Foreign plastic material discovered on fill line.
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FDA
H-0587-2026
|
Food | High |
Mar 25, 2026
Recall: Feb 17, 2026
|
Details |
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Butter Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner
Positive Salmonella contamination
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FDA
H-0573-2026
|
Food | High |
Mar 25, 2026
Recall: Feb 26, 2026
|
Details |
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CLOVER SONOMA SOUR CREAM NET WT 8OZ UPC 0 70852 61800 5 & 16OZ UPC 0 70852 61500 4 DISTRIBUTED BY: CLOVER-STORNETTA FARMS LLC PETALUMA, CA 94952
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
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FDA
H-0580-2026
|
Food | High |
Mar 25, 2026
Recall: Feb 21, 2026
|
Details |
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FDA
H-0577-2026
|
Food | High |
Mar 25, 2026
Recall: Feb 24, 2026
|
Details | |
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Wawa Chocolate Low-fat Milk 16 oz , (Pint) Plastic bottle .Store Refrigerated
Foreign plastic material discovered on fill line.
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FDA
H-0588-2026
|
Food | High |
Mar 25, 2026
Recall: Feb 17, 2026
|
Details |
|
Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.02 oz 2 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed silver metallic bag with a front and back sticker for the labels; Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 150mg total 7-Hydroxymitragynine per container (10 Packets x 2 Tablets Each) 7.5mg 7-OH per tablet/serving, LEM
A sample of the product had the active ingredient in a quantity greater than the labeled specification.
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FDA
H-1107-2026
|
Food | High |
Mar 25, 2026
Recall: Feb 13, 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.
New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.
Recent recall pages are date-driven. Use the published date and recall date to understand whether an alert is new, newly classified or recently updated.
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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