Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 351 - 375 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as "bettergoods Lemon Alfredo Fettuccine, MADE IN ITALY, NET WT 22 OZ, BEST if Used By: SEP 21 2027 L6081A, UPC 194346442706, DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716 PRODUCT OF ITALY Contamination with Listeria monocytogenes	FDA H-0014-2027	Food	High	Oct 14, 2026 Recall: Sep 24, 2026	Details
Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA, INC., AMERICAN CANYON, NAPA VALLEY, CA 94503 PRODUCT OF GREECE UPC: 073214003280 Potential contamination with foreign objects: mice.	FDA H-0007-2027	Food	High	Oct 14, 2026 Recall: Sep 19, 2026	Details
Saint Francis Apizza Frozen Cheese Pizza, Net Weight: 17 oz. (482g), packaged individually in vacuum-sealed plastic, UPC: 6 66186 27759 1 Undeclared soy allergen: soybean oil and soy lecithin	FDA H-0022-2027	Food	High	Oct 14, 2026 Recall: Oct 1, 2026	Details
Croissant; packaged in cardboard box; Ingredients: King Midas Special (Wheat flour, niacin, reduced iron, thiamine mononitrate, riboflavin, folic acid, malted barley flour), Veribest Pastry flour (Wheat Flour), Unsalted Butter, Milk, Water, Granulated Sugar, Yeast, Salt, eggs; Contains: Wheat, Milk Egg was not declared in the Contains statement.	FDA H-0027-2027	Food	High	Oct 14, 2026 Recall: Sep 4, 2026	Details
WinCo Foods Salsa Bean Dip Express Tray is packaged in a foil bottom container with clear plastic lid. Net Wt. 54oz. UPC 2 67173 510983. WinCo Foods Salsa Bean Dip Tray 16inch (sold by catering special order only) is packaged in plastic tray container with clear plastic dome lid. Net Wt. 104oz. UPC 2 67240 ######. Both products sold refrigerated with a shelf life of 4 days from package date. Distributed by WinCo Foods 650 N. Armstrong Place Boise, ID. Bean Dip Trays contains recalled Peperoncini (pepper) which was recalled due to pest issue.	FDA H-0008-2027	Food	High	Oct 14, 2026 Recall: Sep 20, 2026	Details
LEASA Alfalfa Sprouts; packaged in plastic clamshell containers; KEEP REFRIGERATED; NET WT. 6 OZ. (170g); Grown & Packaged by: LEASA Industries Co., Inc., Mami FL 33147; Product of USA; UPC: 0 75465 11111 0 Seeds may have been contaminated with E.coli	FDA H-0003-2027	Food	High	Oct 14, 2026 Recall: Sep 4, 2026	Details
X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by FutuPro S.A.S., Colombian Industry; Distributed by Natur Fuel, 2725 Armstrong Avenue, Clermont, FL 34714. Product contains undeclared Sildenafil and Tadalafil.	FDA H-0016-2027	Food	High	Oct 14, 2026 Recall: Sep 14, 2026	Details
Chocolate Chip Cookies packaged in a cardboard box; Ingredients: King Midas Special (Wheat flour, niacin, reduced iron, thiamine mononitrate, riboflavin, folic acid, malted barley flour), Dark Chocolate Chip (sugar, unsweetened chocolate, cocoa butter, soy lecithin, ground vanilla beans), Unsalted Butter, Dark Brown Sugar, Wheat flour, Eggs, Salt, Baking Powder, Baking Soda, Veribest Pastry flour (Wheat Flour); Contains: Milk, Wheat, Eggs; JK Patisserie & Bakery LLC DBA Le Petit Paris Soy was not declared in the Contains statement.	FDA H-0026-2027	Food	High	Oct 14, 2026 Recall: Sep 4, 2026	Details
Saint Francis Apizza Frozen Pepperoni Pizza, Net Weight: 17 oz. (482g), packaged individually in vacuum-sealed plastic, UPC: 6 66186 27762 1 Undeclared soy allergen: soybean oil and soy lecithin	FDA H-0021-2027	Food	High	Oct 14, 2026 Recall: Oct 1, 2026	Details
QUESO PALMITA. Generic Name: Pastel de Queso (Cheese Pie). Intended use: Human consumption. Condition: Frozen. Shelf life or expected life: 90 days. Type of packaging: Vacuum, resealable package. Net weight: 1.2 lbs. UPC: 094922980045. Undeclared milk, cheese declared	FDA H-0015-2027	Food	High	Oct 14, 2026 Recall: Sep 15, 2026	Details
PLASTICS TRAY; Model/Item Number (Kit): EURO053; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0100-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
Passport Series Patient Monitor. Operator's Manuals: 8 / 12 / 12M / 17M / V Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions	FDA Z-0114-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
HEART PREP TRAY; Model/Item Number (Kit): MECV97W; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0102-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
PACK OPEN HEART CFH; Model/Item Number (Kit): 1. UFCF004-06, 2. UFCF004-07; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0097-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
TufTex¿ Over-the-Wire Embolectomy Catheter; Catalog Number: E1651-88; Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing.	FDA Z-0117-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 28, 2026	Details
T1 Patient Monitor. Operator's Manual: T1 Patient Monitor Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions	FDA Z-0116-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
Sperm Ab ELISA; Model/Catalog Number: EIA-1826; Product Description: Sperm Ab ELISA (96 well plate test); Potential for false negative patient results.	FDA Z-0082-2027	Medical Device	High	Oct 14, 2026 Recall: Jul 2, 2026	Details
Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250; Intellijoint HIP, Portable System, REF: 000-0249 A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro battery, subject to an Apple battery recall, that may overheat and pose a fire safety risk.	FDA Z-0119-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 28, 2026	Details
Brand Name: ADAPTABLE Beach Chair Product Name: Beach Chair surgical patient positioner Model/Catalog Number: 804-33-300 (Enovis); 3105-400-030 (Stryker); internal BC-0001 / BC-0220 Software Version: N/A Product Description: Surgical beach-chair positioner that mounts to the accessory rails of the OR table leg section to elevate and support the patient's upper body in the upright (beach chair) position during surgical procedures. Component: No, finished device. The failure is in the BC-0105, subcomponent. Due to a manufacturing issue (inadequate weld) for patient head positioning system.	FDA Z-0076-2027	Medical Device	High	Oct 14, 2026 Recall: Jul 24, 2026	Details
LAPAROSCOPIC PROSTATECTOMY; Model/Item Number (Kit): NIHB0036-07; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0099-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
BeneView Series. Operator's Manuals: T5 / T8 Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions	FDA Z-0113-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12 Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions	FDA Z-0115-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
DxC 500 AU Clinical Chemistry Analyzers: 1. AU w/out ISE, Part No. C63519 2. AU w/ISE, Part No. C63520 Beckman Coulter has identified a software issue affecting DxC 500 AU Clinical Analyzers when testing plasma samples. Following user configuration of a Clinical Chemistry test to use units different from the system default, a subsequent configuration change and activation of the draft configuration in the System Configuration page may cause the analyzer to revert the test units to the system default setting without notifying the user. The system does Pre-Review Reminders Include OII and [email protected] in any discussions on change/elevation of recalls to Class I classification and situations involving additional public communications (FDA and/or firm issued). Post-Review Reminders Final Check: Ensure your documentation accurately reflects the final recommendation prior to signature. Complete CTS: Recall Product tab, Additional Recall Event Info, Regulation, and Act. Upload PDFs of Consult, Review Memo, and Classification Letter for Class I Recall in DocMan. [Click to enter extra reminder]To add reminders, type the reminder in the text field to the left then press the Tab key. Doc ID 03534.05.06 2 of 8 not provide a warning or notification to alert the user that the configured units have reverted to the default units. This issue can result in falsely elevated reported results.	FDA Z-0084-2027	Medical Device	High	Oct 14, 2026 Recall: Sep 2, 2026	Details
Alphenix INFX-8000C/B5 Loosening of the bolts securing the longitudinal movement mechanism may cause the tabletop to shift, resulting in [positional/imaging/patient] misalignment and a longitudinal motion error	FDA Z-0108-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 26, 2026	Details
HALYARD Laparoscopy Comprehensive Pack II REF: 49332 Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter	FDA Z-0077-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 26, 2026	Details

Showing 351 - 375 of 4,622 product recalls

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Product Recalls Today

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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.

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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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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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