Back to recall look-up

Recall archive

94,421 stored notices, from Jun 20, 2012 to Sep 26, 2026.

31,892 recalls · page 207 of 1329

Medical devices

Reported Nov 6, 2024

smith&nephew LEIGON OXINIUM CONSTRAINED NONPOROUS FEMORAL COMPONENT, SIZE 3 LEFT, REF 71421163; PROSTHESIS, KNEE,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smith & Nephew Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

CADD-Solis Li-ion Rechargeable Battery Packs, REF 21-2160-XX, which are also sold as a component of the following CADD…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2024

Sprouts Chicken Street Taco, 6 taco, perishable item kept under refrigeration, packaged in a plastic tray with plastic…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sprouts Farmers Market

FDA (openFDA food enforcement)

Food

Reported Nov 6, 2024

Los Andes Foods Sweet Corn Pancakes, Cachapas de Maiz, NET WT. 24 Oz., 5 units, KEEP REFRIGERATED

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Tipical Latin Food, Corp. dba La Pradera

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2024

Product Name: Insight Base Flex - 8, Ref 608-3TX; The device consists of a sterile Snap that includes reflective…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Trackx Technology Inc.

FDA (openFDA device enforcement)

Consumer products

Reported Nov 6, 2024

VitalityVita recalls VitalityVita Marketed as Dietary Supplement due to Undeclared Sildenafil and Diclofenac

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

VitalityVita

FDA (recalls & safety alerts)

Medical devices

Reported Nov 6, 2024

Brand Name: Vial2Bag Advanced¿ Product Name: Vial2Bag Advanced¿ 20mm Admixture Device Model/Catalog Number: 6070030…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

West Pharmaceutical Services AZ, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

1) Flex Extenders, 5.2" x 15mm OD x 15mm ID REF S6411P 2) Flex Extender, 5.2" x 15mm OD x 22/15mm ID REF 7 5132 The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Westmed, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2024

New Horizen Gourmet BBQ Pulled Chicken Sandwich on Everything Bialy; KEEP FROZEN; COOK & SERVE; Cooking Instructions:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Whitsons Food Service (Bronx), LLC

FDA (openFDA food enforcement)

Food

Reported Nov 6, 2024

The outer package of the recalled product, Shirakiku Korean Seasoned Seaweed Korean Seaweed, is INCORRECTLY labeled as…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Wismettac Asian Foods, Inc.

FDA (openFDA food enforcement)

Consumer products

Reported Nov 5, 2024

Boulla LLC recalls Boulla LLC Marketed as Dietary Supplement due to Undeclared Sildenafil and Diclofenac

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Boulla LLC

FDA (recalls & safety alerts)

Food

Reported Nov 5, 2024

Savencia Cheese USA recalls Aldi, La Bonne Vie and others Soft ripened cheeses due to Potential Foodborne Illness – Listeria monocytogens

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Savencia Cheese USA

FDA (recalls & safety alerts)

Food

Reported Nov 2, 2024

HH Fresh Trading Corp of California recalls HH Fresh Trading Enoki Mushrooms due to Potential to be contaminated with Listeria monocytogenes.

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

HH Fresh Trading Corp.

FDA (recalls & safety alerts)

Consumer products

Reported Oct 31, 2024

HALO Recalls Tumblers with Metal Straws Due to Laceration Hazard; Sold Exclusively at Wawa Stores

High riskUsing this product could cause serious injury, illness or death — stop using it now.

HALO Branded Solutions Inc.

CPSC

Consumer products

Reported Oct 31, 2024

Harbor Freight Tools Recalls Bauer 4-Gallon Battery-Powered Backpack Sprayers Due to Fire Hazard

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Harbor Freight Tools

CPSC

Consumer products

Reported Oct 31, 2024

Humane Recalls Charge Case Accessory for Ai Pin Due to Lithium Battery Fire Hazard

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Humane Inc.

CPSC

Consumer products

Reported Oct 31, 2024

Manhattan Comfort Recalls Floating Wall Theater Entertainment Centers and Panels Due to Injury Hazard

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Manhattan Comfort Inc.

CPSC

Consumer products

Reported Oct 31, 2024

Polaris Industries Recalls Ranger XP Kinetic Recreational Off-Road Vehicles (ROVs) Due to Fire and Crash Hazards

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Polaris Industries Inc.

CPSC

Food

Reported Oct 31, 2024

R. Walters LLC dba Elevation Foods recalls Hannaford Seafood Salad due to Contains an undeclared soy allergen.

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

R. Walters LLC dba Elevation Foods

FDA (recalls & safety alerts)

Consumer products

Reported Oct 31, 2024

Sanven Technology Recalls Vevor Baby Gates Due to Entrapment Hazard; Violation of Federal Regulations for Gates and…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Sanven Technology Ltd.

CPSC

Medical devices

Reported Oct 30, 2024

AD-TECH Spencer Probe Depth Electrode, REF SD04R-AP58X-000 4-Contact 1.12mm (A style) Depth Electrode

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ad-Tech Medical Instrument Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Oct 30, 2024

OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL OZ (473 mL) bottle, Akron…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Akron Pharma, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Oct 30, 2024

bk3000, model #2300-11; bk3500, model #2300-41; bk5000, model #2300-61; and bkActive 2300, model #2300-66, ultrasound…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

B-K Medical A/S

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2024

Welch Allyn Life2000 Ventilation System, REF MS-01-0118, within exterior carton codes: 1) BT-20-0002, 2) BT-20-0002A,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Baxter Healthcare Corporation

9 more products in this recall

FDA (openFDA device enforcement)

RecallNow is not a government agency. Every notice above is published by the FDA, USDA FSIS, or CPSC and links back to its source. Back to the look-up