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 cautionVehicle
MERCEDES-BENZ SPRINTER (VS30) (2020) recall — Service Brakes, Hydraulic
Daimler Vans USA recalls one 2020 Mercedes-Benz Sprinter with incorrect-size brake discs that may extend stopping distance and increase crash risk. Free brake disc replacement available.
Mercedes-BenzMar 11, 2021 - Lower riskMedical device
Arthrex, Inc. recalls Tibial Opening Wedge Osteotomy Plate, Titanium, 15.0 mm - Product Usage: use in treatment of non-union, mal-union, and
Arthrex recalls titanium tibial plates with confused part numbers that could lead to incorrect use in bone treatments. Affected items have specific part and lot codes.
ArthrexMar 11, 2021 - Use cautionMedical device
Stryker Spine recalls Tritanium X TL Instruments - intervertebral fusion device with bone graft, lumbar. Catalogs:TL Inserter (580220100), TL
Stryker Spine recalls specific lumbar intervertebral fusion instruments due to potential device failure during spinal surgery. Affected items include TL Inserter, Draw Rod, and Syringe Plunger components with UDI codes listed.
Stryker SpineMar 11, 2021 - UnratedMedical device
Krishe Inc recalls Dasky Disposable Sampling Tube, REF VSM02, Contents: Transport Media - 50, Nasal swab - 50, Package Insert - 1, IVD, CE
Krishe recalls Dasky Disposable Sampling Tubes (REF VSM02) due to missing FDA verification for virus transport media. All lots affected; no remedy stated.
KrisheMar 11, 2021 - Lower riskMedical device
LIEBEL-FLARSHEIM COMPANY LLC recalls HydraVision Digital Imaging System Product ID/Reorder Number: 705559 (65KW)
LIEBEL-FLARSHEIM recalls HydraVision Digital Imaging Systems with Product ID 705559 (65KW) and 705560 (80KW) due to potential overestimation of radiation dose. This may lead to unnecessary radiation exposure during medical procedures.
LIEBEL-FLARSHEIMMar 11, 2021 - Stop using nowDrug
Sagent Pharmaceuticals Inc recalls Phenylephrine HCl Injection, USP, 10 mg per mL, 1 mL per Single-Dose Vial packaged in 25 x 1 mL Single-Dose Vials per
Sagent Pharmaceuticals recalls specific lots of Phenylephrine HCl Injection due to lack of sterility assurance from loose crimped vial overseals.
Sagent PharmaceuticalsMar 11, 2021 - UnratedDrug
Breckenridge Pharmaceutical, Inc recalls Omeprazole Delayed-Release Capsules, USP, 20 mg, 1000 count bottles, Rx Only, distributed by Breckenridge
Breckenridge Pharmaceutical recalls 20mg Omeprazole Delayed-Release Capsules due to stability testing showing unknown impurities. This may affect drug safety for patients using prescription medication.
BreckenridgeMar 11, 2021 - Stop using nowDrug
Ferring Pharmaceuticals Inc recalls ZOMA-Jet 10 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 10 mg vial,
Ferring Pharmaceuticals recalls 1,569 ZOMA-Jet 10 Demonstration Kits because the device may break apart. Check lot numbers and UPC.
Ferring PharmaceuticalsMar 11, 2021 - Lower riskFood
Mindo Chocolate Makers LLC recalls Mindo COFFEE TOFFEE CHOCOLATE BAR, 75 gram / 2.65oz UPC code 805993900527. Also sold in 12 count and 6 count cartons
Mindo recalls coffee toffee chocolate bars due to undeclared milk content. Affected bars have UPC 805993900527, sold in 75g bars, 6-count and 12-count cartons. Consumers should check lot numbers 190310-210310.
MindoMar 11, 2021 - Use cautionFood
Whole Foods Market recalls Whole Foods Market Cranberry Biscotti PLU 41712 packaged in a clear plastic clam shell container
Whole Foods Market recalls cranberry biscotti with undeclared pistachios. Stop using if you have the product with PLU 41712 sold through April 2021.
Whole Foods MarketMar 11, 2021 - Stop using nowConsumer product
Melaleuca Recalls Three-Wick Revive Candles Due to Fire and Burn Hazards (Recall Alert)
Melaleuca recalls Revive Three-Wick Soy Candles due to fire and burn hazards from high flames. Stop using immediately and discard products to prevent injuries.
Melale:ucaMar 11, 2021 - Use cautionConsumer product
KTM and Husqvarna Motorcycles Recall Closed Course Competition Motorcycles Due to Crash Hazard (Recall Alert)
Recalled 2021 KTM SX-E 5 and Husqvarna EE-5 competition motorcycles have water in battery causing short circuits and crash risks. Stop riding and contact dealer for free repair.
KTMMar 11, 2021 - Lower riskMedical device
Oscor, Inc. recalls AngioDynamics SafeSheath ULTRALITE 10F, Model Number VI10 - Product Usage: intended for the introduction of various
Oscor recalls AngioDynamics SafeSheath ULTRALITE 10:10F model VI10 due to potential open seal on sterile product. This could compromise sterility during medical procedures.
OscorMar 10, 2021 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Ysio X.pree, Model Number: 11107464 - Product Usage: A Digital X-Ray System generate Xray images from the whole body
Siemens recalls Ysio X.pree digital X-ray systems (model 11107464) due to potential display of previous patient images during image recovery, risking misdiagnosis. Affected units have specific serial numbers.
SiemensMar 10, 2021 - Lower riskMedical device
Remel Inc recalls Remel Haemophilus Test Medium(100mm) 10/PK, REF: R01503 Remel Haemophilus Test Medium (HTM) is a solid medium
Remel recalls Haemophilus Test Medium (10/PK) due to potential light growth zones causing measurement errors in antimicrobial tests. Affected lots expire Feb 2021.
RemelMar 10, 2021 - Use cautionDrug
China Gel Inc recalls CHINA-GEL WHITE (Camphor 3.00%, Menthol 5.00%), A TOPICAL PAIN RELIEVER, packaged in a) 2 oz(56.8g) Tube, 76305-301-13
China-Gel Inc recalls China-Gel White topical pain reliever due to CGMP deviations and potential contamination with B. cepacia. Check lot numbers for details.
China-GelMar 10, 2021 - Lower riskDrug
PNHC, LLC. recalls heal the world, moisturizing original hand sanitizer, Non-Sterile Solution, Alcohol Antiseptic, 70% Topical Solution,
Heal The World recalls 70% alcohol hand sanitizer sold in water bottle-style containers due to confusing labeling. This may lead to accidental ingestion. Affected products have specific lot numbers and expire 5/2022.
Heal The WorldMar 10, 2021 - Lower riskDrug
Sanit Technologies, LLC dba Durisan recalls Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing Wipes, 0.13%, 160-count canister; Sanit
Durisan recalls 160-count antimicrobial hand wipes due to contamination with Burkholderia and mold. Affected lots have specific serial numbers and expiration dates.
DurisanMar 10, 2021 - Lower riskFood
Tippins recalls Tippin's Country Gravy, Net Wt 16 OZ, Keep Refrigerated, Tippin's Gourmet Pies LLC, Kansas City, KS UPC 6 80816 12023 1
Tippins recalls 16oz refrigerated gravy due to premature spoilage reported by consumers. Products may become unsafe if not stored properly.
TippinsMar 10, 2021 - Stop using nowConsumer product
Lifetime Products Recalls 6-Foot Seminar Tables Due to Injury Risk
Lifetime Products recalls 6-foot seminar tables with model #80176 due to risk of collapse. The tables have gray metal frames and white plastic tops. Consumers should stop using and get a free repair bracket.
Lifetime ProductsMar 10, 2021 - Use cautionConsumer product
Hillsdale Furniture Recalls Jennings Counter and Bar Stools Due to Fall Hazard
Hillsdale Furniture recalls Jennings counter and bar stools with date codes from 08/2020 to 01/06/2021 due to risk of seat breaking off and causing falls. Consumers must stop using and contact for free repair.
Hillsdale FurnitureMar 10, 2021 - Use cautionVehicle
FOREST RIVER BERKSHIRE (2021) recall — Electrical System
Forest River recalls 2021 Berkshire RVs with unsealed mini-breakers that could spark in battery compartments, risking fire. Dealers will install free sealed breakers.
Forest RiverMar 9, 2021 - Use cautionVehicle
COACHMEN NOVA (2021) recall — Electrical System
Forest River recalls 2021-2022 Coachmen Nova motorhomes with faulty AGM battery that may allow hydrogen gas entry. Owners must have dealer install free lithium battery fix by November 2021.
Forest RiverMar 9, 2021 - Lower riskMedical device
Medtronic Neuromodulation recalls A610 Clinician Programmer Application for Deep Brain Stimulation Clinician Programming Guide Percept PC Model B35200
Medtronic recalls specific versions of its Percept PC clinician programmer software due to cycling and log fill problems that could cause crashes when copying settings or reading logs.
MedtronicMar 9, 2021 - Use cautionDrug
ICU Medical Inc recalls 0.9% SODIUM CHLORIDE Irrigation, USP 1000 mL Semi-Rigid Bottle, Rx only, Manufactured for ICU Medical, Inc., Lake
ICU Medical recalls 0.9% Sodium Chloride Irrigation bottles due to confirmed particulate matter in some units. Affected lots expire April 2023; check NDC 0990-7138-09 for details.
ICU MedicalMar 9, 2021 - Lower riskDrug
Cardinal Health Inc. recalls Tremfya (guselkumab) Injection, 100 mg/mL, one single-dose prefilled syringe per carton, Rx only, Manufactured by:
Cardinal Health recalls Tremfya (guselkumab) injections due to temperature abuse risks. This product may be unsafe if exposed to high temperatures.
Cardinal HealthMar 9, 2021 - Use cautionVehicle
KENWORTH T440 (2021) recall — Fuel System, Diesel
PACCAR recalls 2021 Kenworth T440 trucks with Cummins L9 diesel engines due to potential fuel leaks near ignition sources that could cause fire. Owners must contact PACCAR for free fuel hose replacement.
PACCARMar 8, 2021 - Use cautionMedical device
Arrow International Inc recalls Arrow OnControl Bone Lesion Biopsy System Tray-11 ga 10 cm Access/13 ga 14 cm Biopsy, Product Code: 9464-VC-006 (US)
Arrow recalls OnControl Bone Lesion Biopsy System Tray (Product Code 9464-VC-006) due to difficulty inserting biopsy ejector rod, risking repeat procedures. Affected units sold in US/EU with specific lot numbers.
ArrowMar 8, 2021 - Use cautionMedical device
BIOTRONIK Inc recalls BIOTRONIK Ilestro 7 VR-T, DF-1, REF 383578, UDI: 04035479125349 - Product Usage: intended to provide ventricular
BIOTRONIK recalls Ilestro 7 VR-T defibrillators with serial numbers starting 60713356-60803564 due to potential premature battery depletion. This may cause device failure during critical heart rhythm treatments.
BIOTRONIKMar 8, 2021 - Stop using nowDrug
Akorn, Inc. recalls Gabapentin Oral Solution, 250 mg/5 mL, 5 mL per unit dose cup, four unit dose cups per tray, For Institutional Use
Akorn recalls Gabapentin Oral Solution (250mg/5mL) for potential impurities that could cause serious injury. This product is for institutional use only and requires immediate action.
AkornMar 8, 2021
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83,613 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.