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Recall archive

94,391 stored notices, from Jun 20, 2012 to Sep 23, 2026.

31,892 recalls · page 130 of 1329

Consumer products

Reported Aug 7, 2025

Monica Vinader Recalls Select 14k Yellow Gold Mini Heart Chain Bracelets, Necklaces, and Stud Earrings Due to High…

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

Monica Vinader Inc.

CPSC

Consumer products

Reported Aug 7, 2025

TEMI Go Basketball Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violates Small Ball Ban; Sold on…

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

Shan tou shi bei bei jia mao yi you xian gong si dba TEMI Toys

CPSC

Consumer products

Reported Aug 7, 2025

Fieldsheer Apparel Technologies Recalls Heated Socks Due to Injury Hazard

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

Tech Gear 5.7 Inc., dba Fieldsheer Apparel Technologies

CPSC

Medical devices

Reported Aug 6, 2025

3M Ranger Irrigation Fluid Warming Set, REF 24750

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

3M Company

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

Automated Impella Controller (AIC), used in left heart support blood pump, including the following: 1. Impella…

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

Abiomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

Molding Equipment. WCM series. Model WCM-330GL-i

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

Apic Yamada America

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

BostonSight SCLERAL Lens

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

Boston Foundation For Sight

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 6, 2025

NH EUROPEAN STYLE BUTTER BLEND, BUNGE, NET WT 1 LB, MFD IN USA BY: Bunge Oils, Chesterfield, MO 63017, packed in white…

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

Bunge North America Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 6, 2025

Casa Mamita, Churro Bites Filled with Chocolate Hazelnut Cream, 7.5 oz , Cardboard Box, 12 boxes per case, Keep Frozen…

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

Camerican International Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 6, 2025

Precision Sampling Set, REF: C20206 for use with the CoSense End-Tidal Carbon Monoxide Monitor

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

Capnia Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 6, 2025

DFA Dairy Brands, LLC recalls Friendly’s Cookies and Cream Ice Cream due to Undeclared wheat and soy allergens

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

DFA Dairy Brands, LLC

FDA (recalls & safety alerts)

Medical devices

Reported Aug 6, 2025

SafeStar 90 Plus Filter. Bidirectionally breathing system filter.

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

Draeger, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Aug 6, 2025

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj,…

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

FDC Limited

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 6, 2025

LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site (Qty 25). Product Code: SET-0013-25.

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

Fresenius Kabi USA, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

ASPRIRE Cristalle Mammography System (cleared under K212873) installed with the ASPIRE Cristalle Digital Breast…

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

FUJIFILM Healthcare Americas Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

Breathing circuit set, coaxial, 1.80 m, with flow sensor and expiratory valve set, REF: 260128, used with HAMILTON-C1,…

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

Hamilton Medical AG

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The HeartSine samaritan¿ PAD (Public Access…

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Drugs

Reported Aug 6, 2025

Lorazepam Injection, USP, 2 mg/mL, 25 x 1mL vials/carton, Rx Only, Manufactured by: Hikma Berkeley Heights, NJ 07922,…

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

Hikma Pharmaceuticals USA Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 6, 2025

The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to store, sterilize, verify Drill Stop…

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

Implant Direct Sybron Manufacturing LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

Brand Name: Celsior Cold Storage Solution Product Name: Celsior Cold Storage Solution Model/Catalog Number: 533682…

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

Institut Georges Lopez

FDA (openFDA device enforcement)

Food

Reported Aug 6, 2025

Drycapot cookie, net weight: 1.15 oz UPC#: 4 942737 210191

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

Jalux America Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 6, 2025

IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal…

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

LTS Therapy Systems, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Aug 6, 2025

Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg, 100 Capsules bottle, Rx Only, Manufactured for: Lupin…

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

Lupin Pharmaceuticals Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 6, 2025

Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.

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

Maquet Cardiopulmonary GmbH

FDA (openFDA device enforcement)

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