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- Lower riskFood
B&G Foods North America, Inc recalls Food Club Garlic Powder, 5.37 ounce bottles, 12 bottles per case. " Best 324A0 C By NOV 19 22 / Best 325A0 By NOV 20 22
B&G Foods recalls 12-bottle cases of garlic powder that accidentally contained bacon-flavored bits with soy, an undeclared allergen. Consumers should check labels for best dates and contact the company for details.
B&G FoodsDec 22, 2020 - Lower riskFood
Country Fresh Orlando, LLC recalls Party Tray Vegetables with Ranch Dip, packaged in 40 oz (2.5 LBS) plastic tray with lid, UPC 3825911509.
Country Fresh recalls Party Tray Vegetables with Ranch Dip due to undeclared egg allergen. Consumers should check UPC 3825911509 and lot code 020NFU2001 for affected items.
Country FreshDec 22, 2020 - Lower riskFood
GH Foods CA LLC recalls Spinach and Orzo Pasta Kit 2/5 lb. UPC: 20826766840209 Sold at Whole Foods Stores
GH Foods recalls spinach and orzo pasta kit (UPC 20826766840209) sold at Whole Foods due to missing egg allergen label on scale.
GH FoodsDec 22, 2020 - Stop using nowFood
Rich Products Corp recalls OUR SPECIALTY; Cake Truffles; Variety; Chocolate; Cookies 'N Creme; NO: Artificial Colors, Flavors, or High Fructose
Rich Products Corp recalls Our Specialty Cake Truffles (19.5 oz) due to undeclared wheat, posing allergy risks in OK, MO, NC, MS, LA, KS.
Our SpecialtyDec 22, 2020 - Stop using nowConsumer product
BRP Recalls All-Terrain Vehicles Due to Crash Hazard (Recall Alert)
BRP recalls 2021 Can-Am Outlander and Renegade ATVs after rear wheel separation risks loss of control. Affected vehicles must be stopped and repaired by dealers.
BRPDec 22, 2020 - Use cautionVehicle
BUICK LACROSSE (2013) recall — Suspension
GM recalls 2013 Buick Lacrosse vehicles with rear toe links that may fracture, increasing crash risk. Owners must contact GM for free suspension replacement.
BuickDec 21, 2020 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2022) recall — Service Brakes, Hydraulic
DTNA recalls certain 2022 Thomas Built Saf-T-Liner C2 school buses due to service brake tie bar issues that may increase crash risk. Check if your bus is affected.
Thomas Built BusesDec 21, 2020 - Use cautionVehicle
FREIGHTLINER BUSINESS CLASS M2 (2021) recall — Service Brakes, Hydraulic
Daimler Trucks North America recalls 2021 Freightliner Business Class M2 trucks with potentially unsafe brake tie bars that could increase crash risk. Free inspections and repairs available.
Daimler Trucks North AmericaDec 21, 2020 - Use cautionVehicle
MERCEDES-BENZ SPRINTER 4500 (2020) recall — Service Brakes, Hydraulic
Mercedes-Benz Sprinter 4500 (2020) vehicles with hydraulic brake issues may have air in the brake system, increasing crash risk. Owners must contact DVUSA for free rear brake caliper replacement.
Mercedes-BenzDec 21, 2020 - Use cautionMedical device
Baxter Healthcare Corporation recalls Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set, Bonded Needle-free IV Connector, Neutral Fluid
Baxter recalls ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Sets due to customer reports of tubing separation from the Male Luer Lock Adaptor. Affected units have specific lot numbers and expiration dates.
BaxterDec 21, 2020 - Lower riskMedical device
Smiths Medical ASD Inc. recalls Portex Acapella DH Vibratory PEP Device - Product Usage: a single patient use device that provides Positive Expiratory
Smiths Medical recalls Portex Acap:ell DH Vibratory PEP devices with wrong model in shipping box. This single-use device for respiratory therapy may not fit patients correctly.
Smiths MedicalDec 21, 2020 - Use cautionMedical device
Nihon Kohden America Inc recalls PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No. 01454 RoHS Compliant; PSG-100 Head Box; UDI
Nihon Kohden recalls PSG-1100 Sleep Diagnostic Systems with specific serial numbers due to electrical safety non-conformance with IEC 60601-1 standards. Affected units may pose a risk of electrical shock during sleep studies.
Nihon KohdenDec 21, 2020 - Lower riskMedical device
OMNIlife science Inc. recalls SERF Novae Dual Mobility Cup Insert 49/28-ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup
OMNIlife recalls SERF Novae Dual Mobility Cup Insert 49/28-ApeX-LNK Poly Liner due to higher than acceptable oxidation limits, potentially requiring revision hip surgery.
OMNIlifeDec 21, 2020 - Lower riskMedical device
Hardy Diagnostics recalls Brain Heart Infusion Agar with 6 ug/ml Vancomycin Cat no: G14 Lot no: 472698 Manufactured: 2020-10-29 Expires:
Hardy Diagnostics recalls Brain Heart Infusion Agar with 6 ug/ml Vancomycin (Lot 472698) due to Staphylococcus aureus breakthrough. Affected users should check their lot numbers and contact the company for details.
Hardy DiagnosticsDec 21, 2020 - Use cautionMedical device
Getinge Group Logistics America, LLC recalls Getinge CM320 Series Washer Disinfector - Product Usage: A multi chamber washer disinfector intended for washing,
Getinge recalls CM320 Series washer disinfectors due to potential hose connections breaking, causing water leaks or sprays that could lead to burns or procedural delays. Affected units have specific serial numbers and product codes.
GetingeDec 21, 2020 - Lower riskDrug
Merck Sharp & Dohme recalls Zerbaxa (ceftolozane and tazobactam) 1.5g per vial for injection, Single-Dose vial, Rx only, Manuf. for: Merck Sharp &
Merck recalls Zerbaxa 1.5g injection vials due to sterility test failures in some batches. Five batches tested positive for Ralstonia pickettii. Affected lots include SP1488 through SP1633 with expiry dates up to April 2023.
MerckDec 21, 2020 - Lower riskFood
SUN VALLEY FOODS LLC recalls Material Number: 7002 3/8 Diced Green Chile INGREDIENTS: Green Chilies, Citric Acid PRODUCT OF: MEXICO UNIT OF MEASURE:
Sun Valley Foods recalls 440 lbs of diced green chile due to potential foreign material. Consumers should check packaging for lot SV20217M010170: 50-gallon plastic drums, Mexico.
Sun Valley FoodsDec 21, 2020 - Lower riskMeat & poultry
Perfect Pasta Inc. Recalls Frozen Meat and Poultry Products Produced Without Benefit of Inspection
USDA recalls Perfect Pasta frozen meat and poultry products made without federal inspection. Consumers should not eat these items and dispose of them immediately.
Perfect PastaDec 19, 2020 - Stop using nowMeat & poultry
FSIS Issues Public Health Alert for Ineligible Imported Raw Frozen New Orleans - Roasted Chicken Wings from the Peoples Republic of China
FSIS alerts consumers about ineligible imported raw frozen chicken wings with a false USDA mark of inspection. Do not consume; discard properly.
Chicken ArrivedDec 19, 2020 - Stop using nowMeat & poultry
Nestlé Prepared Foods Recalls Lean Cuisine Baked Chicken Meal Products Due to Possible Foreign Matter Contamination
Nestlé is recalling Lean Cuisine Baked Chicken meals from September 2020 due to possible white hard plastic contamination. Consumers are urged not to consume these products and should discard or return them.
NestléDec 19, 2020 - Use cautionVehicle
KEYSTONE COUGAR (2021) recall — Electrical System
Keystone recalls 2021 Cougar trailers with Solar Prep or OTG Solar Camping Packages due to improper wiring that could cause fire. Owners must have wiring inspected by dealers.
KeystoneDec 18, 2020 - Stop using nowVehicle
FOREST RIVER PUMA (2021) recall — Equipment
Forest River recalls certain 2021 Puma travel trailers due to a fire risk if the outdoor cooktop is stowed while the burner is on. Check your VIN.
Forest RiverDec 18, 2020 - Lower riskMedical device
Alung Technologies Inc recalls ALung Technologies Hemolung Respiratory Assist System (RAS) with CME BodyGuard 323 Infusion Pump(EUA) - Product Usage:
Alung Technologies recalls Hemolung Respiratory Assist System with CME BodyGuard 323 Infusion Pump due to potential delivery inaccuracy in saline flush. Affected units have specific serial numbers.
Alung TechnologiesDec 18, 2020 - Lower riskMedical device
Topcon Medical Systems, Inc. recalls Harmony Referral System (aka Harmony RS)/ Medical Device Data System - Product Usage: intended to be used by trained
Topcon Medical Systems recalls Harmony RS software version 3.1 due to risk of combining patient records when using with specific medical devices. Affected healthcare professionals should contact for remedy.
Topcon Medical SystemsDec 18, 2020 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700 with software version VE20B - Product
Siemens recalls ARTIS Icono biplane and floor systems with VE20B software due to misleading error messages and gaps in the operator manual, which may cause procedures to terminate and switch to alternative x-ray systems.
SiemensDec 18, 2020 - Lower riskMedical device
Smith & Nephew, Inc. recalls VERSABOND AB 40 GRAMS FORMULATION 2, antibiotic infused bone cement, Product Number: 71271440 - Product Usage:
Smith & Nephew recalls VERSABOND AB 40 GRAMS bone cement (Product #71271440) due to potential heat/humidity exposure causing sandy texture. Affected units may have grainy consistency when mixing.
Smith & NephewDec 18, 2020 - Stop using nowMedical device
Hill-Rom, Inc. recalls Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare,
Hill-Rom recalls Liko Multirall 200 overhead lifts with serial numbers < 6511935 (made before Sep 24, 2019) due to Q-Link strap lock not engaging properly, risking patient and lift detachment.
Hill-RomDec 18, 2020 - Lower riskMedical device
Ansh Labs, LLC recalls AnshLabs - SARS-CoV2 IgM ELISA (u-Capture), IVD, REF: AL-1002, kit contents, Ab PLATE 1 X ! Plate, IgM Sample DIL 1 x
Ansh Labs recalls SARS-CoV2 IgM ELISA test kits due to potential false positives/negatives from labeling updates. Affected kits may cross-react with non-COVID strains.
Ansh LabsDec 18, 2020 - Use cautionMedical device
Laerdal Medical (Suzhou) Co., Ltd. recalls Laerdal Compact Suction Unit (LCSU 4), Catalog Numbers 880051, 880061, 881151, 880052, 880062, 881152 - Product Usage:
Laerdal Medical recalls LCSU 4 suction units with catalog numbers 880051-881152. Component failures may cause loss of suction, risking delayed treatment or suffocation in medical emergencies.
LaerdalDec 18, 2020 - Use cautionDrug
KVK-Tech, Inc. recalls Benzhydrocodone and Acetaminophen Tablets, CII, 6.12mg/ 325mg, 100 Tablets, Rx Only, Manufactured for: KVK-Tech, Inc.,
KVK-Tech recalls Batch 15892A of Benzhydrocodone and Acetaminophen Tablets due to failed impurity specifications. Check your bottle's lot number.
KVK-TechDec 18, 2020
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