Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,069 found- Lower riskFood
Five Star Gourmet Foods, Inc. recalls Simply Fresh Salads - Cranberry Walnut Salad with Very Berry Vinaigrette; sweet-tart cranberries & Walnuts, feta
Five Star Gourmet recalls Cranberry Walnut Salad with Very Berry Vinaigrette due to wheat not being declared as an allergen. The product contains wheat from flatbread chips visible through plastic container.
Five Star GourmetNov 16, 2021 - Stop using nowFood
Mountain Meadow Herbs, Inc. recalls Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086
Mountain Meadow Herbs recalls Candida Flush Endotoxin Cleans3 because bottles may become pressurized, risking injury from expelled contents upon opening.
Mountain Meadow HerbsNov 16, 2021 - Use cautionMeat & poultry
Shamrock Foods Company DBA Gold Canyon Meat Company Recalls Raw Ground Beef Products Due To Possible Foreign Matter Contamination
Shamrock Foods recalls raw ground beef patties from Oct 2021 due to possible hard white plastic contamination. Products may be unsafe; throw away or return to store.
Shamrock FoodsNov 15, 2021 - Use cautionMedical device
Datascope Corp. recalls Cardiosave Rescue IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-75, 0998-UC-0800-75, 0998-00-0800-83,
Datascope recalls Cardiosave Rescue IntraAortic Balloon Pumps with specific model numbers due to risk of fluid entering the device, potentially causing system shutdown and unsafe hemodynamic instability.
DatascopeNov 15, 2021 - UnratedDrug
Aurobindo Pharma USA Inc. recalls Carvedilol Tablets, USP, 6.25 mg, 500 Tablets bottle, Rx Only, Distributed by: Aurobindo Pharma USA Inc., 279
Aurobindo Pharma USA Inc. recalls 6.25 mg Carvedilol tablets (NDC 65862-143-05) due to failed impurities and degradation specifications. This Rx-only medication was distributed from 279 Princeton-Hightstown Road, East Windsor, NJ.
Aurobindo PharmaNov 15, 2021 - Lower riskFood
King's Hawaiian Bakery recalls Kings Hawaiian Hawaiian Sweet Hamburger Buns8 buns NET WT 12.8 oz. (362.9 g) UPC 0 73435-06050 Product Number 800020
King's Hawaiian recalls Sweet Hamburger Buns due to potential small plastic foreign material contamination. Consumers should check product details and contact the company for guidance.
King's HawaiianNov 15, 2021 - Stop using nowFood
The Fillo Factory Inc. recalls TaDah! FALAFEL STREET WRAP WITH SPICY BROWN SUGAR HARISSA HUMMUS NET WT. 7.5 OZ. UPC Code:8-5019800307-5
The Fillo Factory Inc. recalls TaDah! Falafel Street Wraps due to undeclared milk, which can cause serious allergic reactions.
TaDah!Nov 15, 2021 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B
Recall of Siemens ACUSON Sequoia ultrasound systems with software version VA25A/B due to measurement error in 2D trace tool potentially causing misdiagnosis. Affected units have specific serial numbers listed.
Siemens Medical SolutionsNov 12, 2021 - Use cautionMedical device
Acclarent, Inc. recalls TruDi NAV Suction Instruments: 0-Degree, REF: TDNS000Z; 70-Degree, REF: TDNS070Z; and 90-Degree, REF: TDNS090Z
Acclarent recalls TruDi NAV Suction Instruments (0°, 70°, 90° models) due to calibration errors that may cause tissue damage or carotid artery injury during surgery. Affected units include specific lot numbers from 2019-2021.
AcclarentNov 12, 2021 - Lower riskMedical device
Cook Inc. recalls Flexor Check-Flo Introducer Ansel Modification Model Number: KCFW-7.0-18/38-45-RB-ANL0-HC Order Number/GPN: G44155
Cook recalls Flexor Check-Flo Introducer Ansel Modification Model KCFW-7.0-18/38-45-RB-ANL0-HC due to mislabeling that may mix 6FR and 7FR devices.
CookNov 12, 2021 - Stop using nowMedical device
Covidien Llc recalls Covidien Sonicision Battery Charger-intended to charge the Sonicision Reusable Battery Pack and to provide information
Covidien recalls Sonicision Battery Chargers with serial numbers MCSB006939 and MCSB006: Risk of electric shock if used with faulty ground circuit. Stop using immediately.
CovidienNov 12, 2021 - Use cautionMedical device
Philips North America Llc recalls Philips Azurion Interventional Fluoroscopic X-ray System with Azurion R2.2 with LUC configuration start-up issue;
Philips recalls Azurion Interventional Fluoroscopic X-ray Systems with specific model numbers due to start-up communication issues and emergency stop recovery problems that may cause movement failures.
PhilipsNov 12, 2021 - Use cautionMedical device
Invacare Corporation recalls Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A)
Invacare recalls AVIVA FX wheelchairs with LiNX Gyro Module firmware 6.1.2 due to potential injury from aggressive deceleration. Affected models include IFX-20R, IFX-20SP, IFX-20MP, IFX-20C, and IFX20WIDE.
InvacareNov 12, 2021 - Use cautionMedical device
Philips North America Llc recalls BV Endura with Software Release 2.3- A mobile, diagnostic X-ray image acquisition and viewing system. Model Number:
Philips recalls mobile X-ray systems with software release 2.3 due to instructions not specifying maximum surface temperature of X-ray tank, which can cause burns.
PhilipsNov 12, 2021 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls 12 HR Allergy & Congestion Relief Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg Antihistamine I Nasal
Dr. Reddy's recalls 12HR allergy relief tablets with failed dissolution specifications. Consumers should check NDC 70000-0518-1 and lot AC2103329G for affected units.
Dr. Reddy'sNov 12, 2021 - Stop using nowDrug
SterRx, LLC recalls MORPHINE SULFATE, in 0.9% Sodium Chloride Injection, 50 mg per 50 mL, (1 mg per mL), Rx only, SterRx, 141 Idaho Ave.,
SterRx recalls morphine sulfate injections due to lack of sterility assurance. This could cause infections if used improperly. Affected products have specific NDC numbers and were sold in New York.
SterRxNov 12, 2021 - Stop using nowConsumer product
VidaXL Recalls Ladders for Above-Ground Pools Due to Fall and Drowning Hazards (Recall Alert)
VidaXL recalls two stainless steel pool ladders for above-ground pools due to risk of falls and drowning. Consumers must stop using and return the ladders for a full refund.
VidaXLNov 12, 2021 - Stop using nowConsumer product
RH Recalls Outdoor Torches Due to Fire Hazard (Recall Alert)
RH recalls outdoor metal torches with hexagonal or knurled canisters that may leak fuel, causing fire. Consumers should stop using and return for refund or credit.
RHNov 12, 2021 - Stop using nowConsumer product
Hanna Andersson Recalls Baby Ruffle Rompers Due to Choking Hazard (Recall Alert)
Hanna Andersson recalls Baby Ruffle Rompers with detachable snaps that pose a choking hazard to young children. Consumers should stop using and return for a full refund.
Hanna AnderssonNov 12, 2021 - Stop using nowConsumer product
Hanna Andersson Recalls Baby Long Sleeve Wiggle Sets Due to Choking Hazard (Recall Alert)
Hanna Andersson recalls Baby Long Sleeve Wiggle Sets with detachable metal snaps that pose a choking hazard to young children. Consumers should stop using and return for full refund.
Hanna AnderssonNov 12, 2021 - Lower riskMedical device
Orchestrate Orthodontic Technologies, Inc. recalls O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing Instructions (model preparation for tooth
Orchestrate Orthodontic Technologies recalls user manuals and data processing instructions due to altered product labeling. Affected software versions require correction to prevent misuse.
OrchestrateNov 11, 2021 - Use cautionMedical device
Medtronic Navigation, Inc. recalls Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software. Synergy Cranial,
Medtronic recalls Stealthstation Cranial Software versions 3.1.1-3.1.2 and 3.1.3 due to potential incorrect biopsy needle positioning during cranial procedures, risking tissue injury and additional surgery.
MedtronicNov 11, 2021 - Stop using nowFood
Oregon Lox Company recalls North Coast Traditional Nova Lox, cold smoked salmon, various net wt. 2-3lb average per side. UPC 008603005200. The
Oregon Lox Company recalls North Coast Traditional Nova Lox salmon products due to potential Listeria monocytogenes contamination. Products sold with UPC 008603005200 may be affected.
Oregon Lox CompanyNov 11, 2021 - Use cautionFood
KRAFT HEINZ FOODS COMPANY recalls Kool-Aid cherry drink mix powder 19 oz. UPC 043000953532 19 oz. UPC 043000034163 63 oz. UPC 043000082201
Kraft Heinz recalls cherry Kool-Aid drink mixes due to potential glass and metal contamination. Check UPCs 043000953532, 043000034163, and 043000082201 for affected products.
Kraft HeinzNov 11, 2021 - Use cautionMeat & poultry
Euro Foods Dba Citterio USA Corp. Recalls Salame Stick Products Due To Possible Salmonella Contamination
USDA recalls 119,091 pounds of Citterio Italian-style salame sticks produced before Oct 25, 2021 due to possible Salmonella contamination. Consumers urged not to consume.
CitterioNov 10, 2021 - Use cautionMeat & poultry
Innovative Solutions, Inc. Recalls Chicken Patty Products Due To Possible Foreign Matter Contamination
USDA recalls 97,887 pounds of Trader Joe's chicken patties with possible bone contamination. Consumers urged not to eat these products and dispose of them safely.
Trader Joe'sNov 10, 2021 - Lower riskMedical device
Velano Vascular recalls PIVO Blood Collection Device 20G, REF: 202-0005
Velano Vascular recalls PIVO Blood Collection Device 20G (REF: 202-0005) due to potential microbial contamination from incomplete sterile packaging. Affected units include specific production lots sold between May 2021 and July 2021.
Velano VascularNov 10, 2021 - Lower riskMedical device
Tapemark Company recalls iontoPATCH On-the-Go Patch Therapy, Transdermal Iontophoretic Drug Delivery System, Extra Strength, 8-HOUR Average Wear
Tapemark recalls extra strength iontoPATCH patches due to incorrect dosage information on pouches. The primary carton label is correct. Consumers should check lot numbers 1131-1 and :1131-2.
TapemarkNov 10, 2021 - Lower riskMedical device
Beckman Coulter Inc. recalls SYNCHRON Systems Cholesterol (CHOL) Reagent, REF: 467825
Beckman Coulter recalls SYNCHRON Cholesterol reagent REF 467825 due to potential errors causing inaccurate cholesterol test results. Affected units may show brown particles or calibration failures.
Beckman CoulterNov 10, 2021 - Use cautionFood
The Coca Cola Company recalls Minute Maid Fruit Punch, 59 fl. oz.(1.8 QT)1.75 L, Unit UPC: 025000047725, Case UPC: 025000047732
Coca-Cola recalls Minute Maid Fruit Punch 59 fl oz bottles with possible metal bolt or washer. Consumers should check UPC codes and contact customer service for details.
Coca-ColaNov 10, 2021
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83,807 recalls tracked · 72,041 explained in plain English · 10,992 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.