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
35,025 found- Use cautionMedical device
STEP-HAR MEDICAL LLC recalls Alaris Pump Module, Model 8100, serviced/repaired by Step-Har Medical with an impacted bezel repair part
Step-Har Medical recalls Alaris Pump Module Model 8100 with impacted bezel repair parts that may cause infusion interruptions. Affected units have specific serial numbers.
Step-Har MedicalFeb 26, 2021 - Lower riskMedical device
Medtronic Inc. recalls Medtronic REF: MMT-7020C Guardian Sensor (3) kit for the following packaging: GS3 SEMI 5PK OUS/ GTIN: 20763000192086,
Medtronic recalls Guardian Sensor kits for inaccurate glucose readings when used with hydroxyurea. Affected kits have specific packaging codes; no remedy provided in recall notice.
MedtronicFeb 26, 2021 - Lower riskMedical device
Heartware, Inc. recalls Instructions for Use and Patient Manual for HeartWare HVAD System. Accompanies these devices: Heartware HVAD pump
Heartware recalls updated instructions for HeartWare HVAD system to address alarms that resolve quickly, which may indicate intermittent issues needing clinician evaluation.
HeartwareFeb 26, 2021 - Use cautionMedical device
Accuray Incorporated recalls CyberKnife Treatment Delivery System - Product Usage: indicated for image-guided stereotactic radiosurgery and
Accuray recalls CyberKnife treatment systems with set screws that can loosen over time, potentially causing the treatment couch to roll. Affected units include specific product codes and serial numbers listed in the recall.
AccurayFeb 26, 2021 - Use cautionMedical device
Biosense Webster, Inc. recalls Biosense Webster, CARTO VIZIGO, Bi-Directional Guiding Sheath, 8.5F (Large) C3, REF: D138503, Rx Only, CE 2797, STERILE
Biosense Webster recalls specific cardiac sheaths for potential minor bleeding or embolism if the hemostatic valve dislodges during use. Affected models include 8. 5F (Large) C3, REF: D138503.
Biosense WebsterFeb 26, 2021 - Lower riskMedical device
Heartware, Inc. recalls Instructions for Use and Patient Manual for HeartWare HVAD System. Accompanies these devices: Heartware HVAD pump
Heartware recalls updated instructions for HVAD system to clarify controller connection verification using a beep instead of audible click. This correction helps users identify proper device connection without confusion.
HeartwareFeb 26, 2021 - Lower riskDrug
Alvogen, Inc recalls Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg, 30 pouches each containing 1 sublingual film, Distributed by:
Alvogen recalls Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg due to low drug potency. This may reduce effectiveness for addiction treatment. Check NDC 47781-355-03, Lot 36924, Exp 6/2021.
AlvogenFeb 26, 2021 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Progesterone Capsules, 200 mg, 100-count bottles, Rx Only, MADE IN FRANCE; Distributed by: Dr. Reddy's Laboratories,
Dr. Reddy's recalls 200mg progesterone capsules (100-count) made in France due to dissolution testing failures. Rx-only product with batch #1399851P1.
Dr. Reddy'sFeb 26, 2021 - Lower riskFood
Westminster Cracker Inc. recalls Old Cape Cod Soup and Chowder Oyster Crackers - 8oz Box, 12 per case - UPC 093215801005; Westminster Bakers Co. Soup &
Westminster Cracker Inc. recalls Old Cape Cod Soup and Chowder Oyster Crackers due to potential hard plastic foreign objects. Consumers should check UPCs and stop using if concerned.
Westminster Cracker Inc.Feb 26, 2021 - Lower riskFood
Laboratorios Pisa Sa De Cv recalls Electrolit Fruit Punch Zero, 625ML/21OZ packaged in a polypropylene bottle with volume capacity of 625mL and with a
Laboratorios Pisa recalls Electrol: 625ml Fruit Punch Zero bottles with undeclared FD&C Red 40. Consumers should check lot numbers M21E366 or M21E367 from January 2024.
Laboratorios PisaFeb 26, 2021 - Stop using nowFood
THE QUAKER OATS COMPANY recalls Quaker Rice Crisps Sweet Barbecue Flavor, 3.03 oz. bag, UPC 0 30000 31984 0
Quaker Oats recalls 3.03 oz bags of Sweet Barbecue Rice Crisps due to undeclared soy. Check your UPC and Best Before date.
QuakerFeb 26, 2021 - Lower riskFood
Taylor Farms Northwest, LLC recalls Item #140804, Egg Salad Croissant Sandwich, Refrigerated, packaged in clear plastic clamshell container. Ready to Eat
Taylor Farms recalls Egg Salad Croissant Sandwiches sold between Feb 27-2021 due to undeclared soy lecithin in margarine. Consumers should check labels for soy lecithin.
Taylor FarmsFeb 26, 2021 - Use cautionFood
J & J Distributing Company recalls tastebuds Taco Platter, Net Wt. 26oz. (738g), UPC 0 38232 31683 5; Net Wt. 15.8oz (448g), UPC 0 38232 33235 4,
J & J Distributing Company recalls two sizes of Tastebuds Taco Platter due to potential Listeria monocytogenes contamination. Consumers should check UPCs and contact the company for details.
J & J Distributing CompanyFeb 26, 2021 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Beef Meatball Products Due to Misbranding and Undeclared Allergen
FSIS public health alert: Whole Foods Market sold beef meatballs with marinara sauce containing undeclared parmesan cheese (milk allergen). Consumers with milk allergies should not consume these products.
Whole Foods MarketFeb 25, 2021 - Use cautionVehicle
JAGUAR F-PACE (2019) recall — Exterior Lighting
Jaguar recalls 2019 F-Pace vehicles with high beam system that doesn't warn driver when active, risking crashes. Owners must update software free by April 2021.
JaguarFeb 25, 2021 - Use cautionVehicle
FORD F-450 (2019) recall — Exterior Lighting
Life Line is recalling one 2020 Ford F450 and one 2017 Navistar Durastar with overly bright LED lights that may cause crashes. Owners get free filter kits to fix the issue.
Life LineFeb 25, 2021 - Stop using nowVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2020) recall — Engine
DTNA recalls 2019-2021 Thomas Built Buses Saf-T-Liner C2 school buses due to engine software errors affecting safety functions. Free recalibration available.
Thomas Built BusesFeb 25, 2021 - Use cautionVehicle
LAND ROVER RANGE ROVER SPORT (2020) recall — Exterior Lighting
Land Rover is recalling 2020 Range Rover Sport vehicles with a high beam system that doesn't alert drivers when high beams are on, increasing crash risk. Owners must contact customer service for free software update.
Land RoverFeb 25, 2021 - Use cautionVehicle
BUICK ENCLAVE (2020) recall — Tires
General Motors recalls 2020 Buick Enclaves with over-cured tires that may cause sudden air loss or tread/belt loss, increasing crash risk. Owners should contact GM for free tire replacement.
BuickFeb 25, 2021 - Use cautionVehicle
BLACK SERIES CAMPERS C12 (2020) recall — Equipment
Black Series is recalling certain 2020-2021 C12, C13, C15, HQ12, HQ15, HQ17, HQ19, HQ19T, HQ21, and HQ22T trailers with Curt emergency breakaway kits. Overloaded electrical systems may cause fire. Owners must have affected components replaced free by dealers.
Black SeriesFeb 25, 2021 - Use cautionMedical device
Biocare Medical, LLC recalls BIOCARE Medical , IntelliPath FLX, Automated Staining Instrument, Ref: " Model Number:IPS0001US and IPS0001INTL
Biocare Medical recalls IntelliPath FLX automated staining instruments with software version 3.5.3.1 due to potential unintended movement that could cause damage or liquid spills. Affected units include specific US and OUS serial numbers.
Biocare MedicalFeb 25, 2021 - Use cautionMedical device
Tenacore LLC recalls Alaris Infusion Pump 8100 Bezel (plastic piece only), Part: TIPA-8100-4410
Tenacore recalls Alaris Infusion Pump 8100 bezel parts (TIPA-8100-4410) sold 2020-2021. Cracking may cause infusion issues. Check your pump for 5-6 SO numbers on bezel.
TenacoreFeb 25, 2021 - Use cautionMedical device
BioMedical Equipment Service Co (BMES) recalls Alaris Infusion Pump Module, Model 8100, serviced/repaired by Biomedical Equipment Service Co. (BMES) with an impacted
BMES recalls Alaris Infusion Pump Module Model 8100 units serviced with non-original bezel repair parts. Cracking posts could cause infusion issues. Check serial numbers listed for affected units.
BMESFeb 25, 2021 - Lower riskMedical device
Dutch Ophthalmic USA, Inc. recalls Disposable Replacement Backflush Brush Needles (23 gauge/0.6mm)-for use in vitreoretinal surgery Product Number:
Dutch Ophthalmic USA recalls 23-gauge backflush brush needles labeled as 20-gauge. Mislabeled needles could cause surgical errors. Check product code 1281.B1D06 for affected items.
Dutch OphthalmicFeb 25, 2021 - Use cautionMedical device
Fenwal Inc recalls Amicus Exchange Kit - Product Usage: intended for use in the collection of blood components and mononuclear cells.
Fenwal recalls Amicus Exchange Kits with leaking centrifuge packs that could cause blood leaks during blood component collection procedures. Affected kits have specific batch numbers and expiration dates.
FenwalFeb 25, 2021 - Lower riskMedical device
Cardinal Health 200, LLC recalls In-View Clear Leggings Sterile
Cardinal Health recalls sterile In-View Clear Leggings due to plastic film manufacturing issues causing drapes to stick, potentially preventing proper application. Affected lots expire through December 2025.
Cardinal HealthFeb 25, 2021 - Lower riskFood
KAREEM MART INC recalls Tahina Sesame Paste packaged in 1lb and 2lb plastic jars and 10kg metal containers; UPC CODES 6215000382207
Kareem Mart recalls Tahina Sesame Paste in 1lb, 2lb plastic jars and 10kg metal containers due to Salmonella contamination. Products with UPC 6215000382207 and specific lot numbers are affected.
Kareem MartFeb 25, 2021 - Use cautionConsumer product
MTIG Productions Recalls deSensua Wintergreen, Birch and Pain Soother Essential Oils Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
deSensua Wintergreen, Birch and Pain Soother Essential Oils lack child-resistant packaging, risking poisoning if young children swallow. Consumers must store safely and get refunds.
deSensuaFeb 25, 2021 - Stop using nowConsumer product
Home Depot Recalls Wood Windsor Dining Chair Sets Due to Fall Hazard (Recall Alert)
Home Depot recalls StyleWell Wood Windsor Dining Chair sets due to fall hazard. The chair back can detach. Stop using immediately and inspect for missing screws.
StyleWellFeb 25, 2021 - Use cautionConsumer product
Dr. Reddy's Recalls Prescription Drug Blister Packages Due to Risk of Poisoning
Dr. Reddy's recalls prescription blister packs that are not child-resistant, posing poisoning risk to young children. Consumers should store safely and get refunds.
Dr. Reddy'sFeb 25, 2021
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