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 riskDrug
STAQ Pharma, Inc. recalls HYDROmorphone HCl PF 10 mg/50 mL (0.2mg/mL) in NaCl, 50 mL in 50 mL Single Dose Syringe, Rx only, STAQ Pharma, Inc.,
STAQ Pharma recalls 50mL single-dose hydro morphine syringes with incorrect morphine sulfate labeling. This could lead to medication errors if used without proper identification.
STAQ PharmaFeb 3, 2022 - Lower riskFood
Whole Foods Market Brand 365, Llc recalls Whole Foods Market Vanilla Short Bread Cookies packaged in clear plastic container with a white scale label applied PLU
Whole Foods Market recalls Vanilla Short Bread Cookies with undeclared egg. Check packaging for PLU 66705 (pack date 1/20/22).
Whole Foods MarketFeb 3, 2022 - Stop using nowFood
Pacific Golden Coast Trading Inc recalls Dried salted plum, packaged in 22 lbs. carton. Product of China.
Pacific Golden Coast Trading Inc. recalls dried salted plums from China with elevated lead levels. Consumers should stop using affected lots due to potential health risks from lead exposure.
Pacific Golden Coast TradingFeb 3, 2022 - UnratedFood
A & E Corrales LLC recalls Saladitos With Chili, Net Weight 16 oz (1lb) with UPC 0661799748162. The product is packaged in ultra clear sealed
A & E Corrales recalls Saladitos With Chili (16oz) due to elevated lead levels. Products packaged in clear zip-lock bags with no expiry date or lot code. Consumers should check UPC 0661799748162 for affected items.
A & E CorralesFeb 3, 2022 - Stop using nowConsumer product
BFG North Carolina Recalls Chest of Drawers Due to Tip-Over and Entrapment Hazards; Sold Exclusively at Rooms To Go (Recall Alert)
River Street Five-Drawer Chests (2018-2021) recalled due to unstable design causing tip-over and entrapment risks for children. Consumers must stop using and contact Rooms To Go for repair, replacement, or refund.
River StreetFeb 3, 2022 - Use cautionVehicle
KIA K900 (2017) recall — Service Brakes, Hydraulic
Kia recalls 2016-2018 K900 and 2014-2016 Sportage vehicles with potential engine fire risk due to hydraulic brake system malfunction. Owners must park away from structures until repair.
KiaFeb 2, 2022 - Use cautionVehicle
PORSCHE TAYCAN (2021) recall — Suspension
Porsche is recalling one 2022 2021 Taycan vehicle due to potential suspension misalignment causing uneven tire wear and crash risk. Free alignment and tire repairs offered.
PorscheFeb 2, 2022 - Use cautionVehicle
KEYSTONE RAPTOR (2021) recall — Tires
Keystone is recalling 2021-2022 Raptor and Montana RVs with certain Sailun tires due to potential belt separation causing loss of vehicle control. Owners must have tires inspected and replaced if needed.
KeystoneFeb 2, 2022 - Use cautionVehicle
ENTEGRA ACCOLADE (2021) recall — Steering
Jayco is recalling certain 2021-2022 Entegra Accolade motorhomes due to loose tie rod clamps that may cause steering loss and crash risk. Owners should contact Jayco customer service for free replacement of tie rod clamp bolts and nuts.
JaycoFeb 2, 2022 - Use cautionVehicle
TIFFIN ALLEGRO RED (2020) recall — Structure
Tiffin is recalling 2020-2022 Allegro Red motorhomes due to potential awning detachment while moving, which could cause crashes or injuries. Owners must have awnings inspected by dealers.
TiffinFeb 2, 2022 - Use cautionVehicle
TESLA MODEL Y (2020) recall — Electrical System
Tesla is recalling 2020 Model Y vehicles with a software error that may reduce defrosting performance, risking driver visibility and crashes. Owners will receive a free over-the-air software update.
TeslaFeb 2, 2022 - Lower riskMedical device
Philips North America Llc recalls Philips Allura (Model Numbers 722010, 722012, 722026, 722027, 722028, 722029, 722035) and Philips Azurion (Model
Philips recalls specific Allura and Azurion models with StentBoost Live R2.0 software that may show incorrect X-ray images from previous runs instead of current patient scans.
PhilipsFeb 2, 2022 - Lower riskMedical device
Ace Surgical Supply Co., Inc. recalls NuOss Collagen Block Size 8mm x 9mm x 9mm- used in filling periodontal and maxillofacial defects. Catalog Number:
Ace Surgical recalls NuOss Collagen Blocks (8mm x 9mm x 9mm) for possible suboptimal bone repair in dental procedures. Affected items have specific catalog and lot numbers.
Ace Surgical SupplyFeb 2, 2022 - Lower riskMedical device
Philips Healthcare recalls Philips StentBoost Live R2.0 application, when used with the Philips Azurion with software release R2.x
Philips recalls StentBoost Live R2.0 software for Azurion systems with R2.x software due to incorrect EPX database configuration causing acquisition to continue after 40 images instead of stopping automatically.
Philips HealthcareFeb 2, 2022 - Stop using nowFood
la fiesta food products recalls La Fiesta brand, Salted Plums with Chili Product. Product is packaged in cello bags, net wt. 1oz. UPC 0 32327 02829 0.
La Fiesta Salted Plums with Chili (1oz cello bags) recalled due to elevated lead levels. Consumers should stop using these products immediately.
La FiestaFeb 2, 2022 - Lower riskFood
El Super Leon Ponchin Snacks, Inc. recalls El Super Leon brand, Dry Salted Plum with Chili, Shelf Stable, packaged in plastic bag, Net Wt 1.05oz, UPC
El Super Leon recalls 144 units of dry salted plum with chili snacks due to potential lead contamination. Consumers should check packaging for UPC 8-52605-00408 or 8-52605-00024 and stop using if concerned.
El Super LeonFeb 2, 2022 - UnratedFood
El Chavito recalls El Chavito¿ Saladitos Dried Salted Plums, net wt. 1.7 oz bag, Individual UPC 859470006049, Master Case UPC
El Chavito recalls dried salted plums with potential lead contamination. All bags and master cases sold with specific UPCs are affected. Consumers should check labels for the listed UPCs and contact the company for details.
El ChavitoFeb 2, 2022 - Stop using nowConsumer product
Maxtrade Recalls All-Terrain Vehicles (ATVs) Due to Injury Hazard and Violations of Federal Safety Standard
Maxtrade recalls Youth Coolster Mountopz ATVs due to excessive speed limits and parking brake failures. Stop using immediately and contact Maxtrade for a free repair.
MaxtradeFeb 2, 2022 - Use cautionConsumer product
Games Workshop Recalls Koyo Bounca The Squig Plush Toys Due to Choking Hazard
Games Workshop recalls KOYO Bounca The Squig Limited Edition Plush toys due to detachable pom-poms posing a choking hazard to young children. Consumers should return for refund or destroy the toy.
Games WorkshopFeb 2, 2022 - Stop using nowConsumer product
D&D Technologies Recalls SureClose READYFIT 180° Hinge-Closer Sets Due to Injury and Drowning Hazards
D&D Technologies recalls SureClose READYFIT 180° Hinge-Closer Sets due to risk of unintended gate access causing injury or drowning for young children. Consumers must stop using and replace the product.
D&D TechnologiesFeb 2, 2022 - Stop using nowConsumer product
Children's Robes Recalled Due to Violation of Federal Flammability Standards and Burn Hazard; Imported by BAOPTEIL; Sold Exclusively on Amazon.com
BAOPTEIL children's robes fail federal flammability standards, risking burns. Recalled items sold on Amazon; return for full refund via prepaid mailer.
BAOPTEILFeb 2, 2022 - Lower riskMedical device
BSN Medical Inc recalls (1) JOBST Compri2, REF 76271-01, containing 2 components, one plastic-wrapped padding and one plastic-wrapped
BSN Medical recalls JOBST Compri2 and lite products due to mislabeled shipping boxes. The hazard involves incorrect labeling of folding boxes within the shipping case, which may cause confusion during use.
BSN MedicalFeb 1, 2022 - Use cautionMedical device
Mevion Medical Systems, Inc. recalls Mevion S250 and S250i Proton Therapy Systems hand pendant (P/N 10263 or P/N 37808)
Mevion recalls S250 and S250i proton therapy hand pendants with risk of unintended motion causing patient injury. Affected units have specific serial numbers and UDI codes.
MevionFeb 1, 2022 - Lower riskMedical device
BioPro, Inc. recalls Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037
BioPro recalls Titanium MPJ toe implants due to unverified MR safety claims. The implant may not be safe for MRI scans as testing was not done on the titanium version.
BioProFeb 1, 2022 - Lower riskFood
Tam's Homemade Biscuits Inc recalls Tam's Homemade Biscuits 8 count packaged in 9 inch round aluminum cake pan 10 pans per case
Tam's Homemade Biscuits recalls 10-pack of 8-count aluminum cake pans due to missing allergen and ingredient statements. Consumers should check batch numbers for affected items.
Tam's Homemade BiscuitsFeb 1, 2022 - Stop using nowFood
The Royal Ice Cream Company Inc. recalls All Ice Cream and Ice Cream products within expiry; manufactured by Royal Ice Cream Company; manufactured in
Royal Ice Cream recalls all products within expiry due to potential Listeria monocytogenes contamination. Consumers should check for manufacturing plant number CT121 or CT #121.
Royal Ice CreamFeb 1, 2022 - Lower riskFood
Honey Heaven Wholesale Inc recalls Organic Roasted Salted Cashews, Net Weight of 6 oz (170g), UPC 6 16316 76283 1. Product is packed in a brown kraft
Honey Heaven recalls organic roasted salted cashews due to mislabeling hazelnuts as cashews. Hazelnuts are visible through the packaging window. Consumers should check for the specific UPC code and product details.
Honey HeavenFeb 1, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Ysiosystem with VC10 software version, Model Number 10281013. Radiographic system
Siemens recalls Ysio radiographic systems with VC10 software version 10281013 due to a software error that may cause unintended tube stand movement, creating collision risk for people or objects.
SiemensJan 31, 2022 - UnratedMedical device
SD Biosensor, Inc. recalls STANDARD Q COVID-19 Ag Home Test STANDARD Q COVID-19 Ag Home Test is a rapid chromatographic immunoassay for the
SD Biosensor recalls STANDARD Q COVID-19 Ag Home Test kits imported illegally into the U.S. that aren't approved for distribution. These tests may not be safe or effective.
SD BiosensorJan 31, 2022 - Lower riskMedical device
Canon Medical System, USA, INC. recalls INFX-8000V. For radiographic and fluoroscopic studies and intervention.
Canon recalls INFX-8000V fluoroscopy systems for potential dose rate exceedance during biplane procedures. Affected units include Alphenix i with software versions 8.0, 9.0, or 9.2 and TFP 1200C FPD. No remedy specified in recall notice.
Canon MedicalJan 31, 2022
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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.