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- Stop using nowConsumer product
Ravin Crossbows Reannounces Recall of White Arrow Nocks Due to Injury Hazard and Additional Incidents; Nearly Two Dozen Serious Injuries Reported
Ravin Crossbows recalls white arrow nocks due to risk of bow discharging while re-nocking, causing injuries. Nearly two dozen serious injuries reported. Consumers must stop using and return for free orange nocks.
Ravin CrossbowsAug 18, 2021 - Use cautionConsumer product
Primark Recalls Scent Stamper Pens Due to Elevated Levels of Benzyl Alcohol; Risk of Skin Irritation
Primark recalls 8-pack Scent Stamper Pens with elevated benzyl alcohol levels that may cause skin irritation. Consumers should stop using and return pens for full refund.
PrimarkAug 18, 2021 - Stop using nowConsumer product
Nordstrom Recalls Children's Socks Due to Choking Hazard
Nordstrom recalls Tucker & Tate children's socks (sizes 5-7) due to risk of choking from detachable pom poms. Affected items include packs with gray, white-blue, and white-red pairs. Customers should stop using and get a refund.
Tucker & TateAug 18, 2021 - Stop using nowConsumer product
Marin Mountain Bikes Recalls Bicycles Due to Fall and Crash Hazards
Marin recalls 20 2021 mountain bike models due to bottom bracket failure risking falls and crashes. Stop using immediately and get free repair.
MarinAug 18, 2021 - Stop using nowConsumer product
Intertex Recalls Blower Fans Due to Fire Hazard
Intertex recalls B-Air VP-33 blower fans (sold before Jan 2018) due to fire risk from overheating capacitors. Affected units have neon yellow boxes and B-Air logos. Get a free repair kit to fix the capacitor.
B-AirAug 18, 2021 - Stop using nowConsumer product
Hallmark Recalls Teethers Due to Choking Hazard
Hallmark recalls 11 styles of wooden teethers with plush attachments sold 2015-2020 due to risk of breaking into small choking hazards for young children.
HallmarkAug 18, 2021 - Use cautionVehicle
NEWMAR NEW AIRE (2021) recall — Fuel System, Diesel
Newmar is recalling 2021-2022 New Aire models with Cummins diesel engines due to potential fuel leaks that could cause fire if near ignition sources. Owners must contact customer service for free fuel hose replacement.
NewmarAug 17, 2021 - Lower riskMedical device
Olympus Corporation of the Americas recalls EVIS EXERA BF-XT160 Bronchofibervideoscope, Model No. BF-XT160
Olympus recalls EVIS EXERA BF-XT160 bronchoscopy scopes due to potential insertion tube leaks causing infection control risks. Affected units sold in the U.S. from 2019 to 2023.
OlympusAug 17, 2021 - Lower riskDrug
RemedyRepack Inc. recalls Carvedilol 25 mg, 180-count bottle, Rx only, Manufactured by Zydus Pharm, Pennington, NJ 08534, NDC 68382-0095-05,
RemedyRepack Inc. recalls 180-count Carvedilol 25mg bottles (Rx only) that accidentally contain Paroxetine tablets due to repackaging error. This could cause unintended medication interactions.
RemedyRepackAug 17, 2021 - Stop using nowConsumer product
Zen Magnets and Neoballs Magnets Recalled Due to Ingestion Hazard
Recall of high-powered magnets due to risk of serious injury if swallowed. Consumers must stop using and contact for refund.
Zen MagnetsAug 17, 2021 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls syngo.CT VA20A, VA30A and VA40A in: syngo.via RT Image Suite / Sim&Go SOMATOM go.Now SOMATOM go.Up SOMATOM go.All
Siemens recalls certain CT scanners that may cause incomplete treatment planning data if structure sets are edited after saving and reopening studies. Affected models include SOMATOM go.Now, go.Up, go.All, and others. No remedy specified in recall notice.
SiemensAug 16, 2021 - Lower riskMedical device
Biodex Medical Systems, Inc. recalls Atomlab 500 Dose Calibrator Software 2.0.00 through Revision 2.0.08, inclusive Model: 086-330.
Biodex recalls Atomlab 500 Dose Calibrator Software 2.0.00-2.0.08 for potential incorrect dose measurements if custom isotopes are deleted without updating dial settings.
BiodexAug 16, 2021 - Lower riskMedical device
Olympus Corporation of the Americas recalls BF-XP60 OES Bronchofiberscope, Model No. BF-XP60
Olympus recalls BF-XP60 OES Bronchofiberscope with updated reprocessing instructions per FDA 2015 guidance. No immediate action needed for safety.
OlympusAug 16, 2021 - Use cautionVehicle
GRAND DESIGN IMAGINE (2021) recall — Power Train
Grand Design is recalling 2021 Imagine trailers with Dexter D30 axles that may have incorrect inner bearings, risking wheel lockup and crashes. Owners must have axles inspected by dealers.
Grand DesignAug 13, 2021 - Lower riskMedical device
Quidel Corporation recalls Lyra Direct SARS-CoV-2 Assay Emergency Use Authorization- Ref: M124. The Lyra Direct SARS-CoV-2 Assay is a real-time
Quidel recalls Lyra Direct SARS-CoV-2 Assay due to potential false negatives in high viral load samples when used with certain PCR machines. Affected units may need retesting or alternative methods.
QuidelAug 13, 2021 - Lower riskMedical device
Greiner Bio-One North America, Inc. recalls VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged
Greiner Bio-One recalls 6ml K2EDTA blood collection tubes with pink caps that may clot during use. Affected lots expire 09/2022 or 11/2022. Stop using immediately to avoid inaccurate blood tests.
Greiner Bio-OneAug 13, 2021 - Use cautionMedical device
IMPERATIVE CARE INC recalls Imperative Care, ZOOM 71 Reperfusion Catheter, REF: ICRC071137, TRX Tip, 137 cm, 6F (.083 in/2.11 mm), .071 in/1.8 mm),
Imperative Care recalls ZOOM 71 Reperfusion Catheters with potential for distal end fracture and detachment. Affected lots include V2014902 through F2113004. Stop using if you have these specific lots.
Imperative CareAug 13, 2021 - Use cautionMedical device
Philips North America Llc recalls The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular and neurovascular
Philips recalls Allura Xper series medical imaging devices due to potential overheating from 480V hospital power, causing reduced X-ray performance and possible burning smell. Affected units have specific serial numbers.
PhilipsAug 13, 2021 - Lower riskDrug
Zydus Pharmaceuticals (USA) Inc recalls Carvedilol Tablets, USP 25 mg, 500 Tablets bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd., India,
Zydus Pharmaceuticals recalls 25mg Carvedilol tablets due to foreign paroxetine tablets found in some bottles. Report of two paroxetine tablets in the bottle poses a potential risk.
Zydus PharmaceuticalsAug 13, 2021 - UnratedDrug
Akorn, Inc. recalls Betamethasone Dipropionate Lotion USP (Augmented), 0.05%, packaged in a) 30 mL bottle (NDC 61748-480-30), b) 60 mL
Akorn recalls 0.05% Betamethasone Dipropionate Lotion USP (Augmented) due to an unknown impurity. This topical medication, sold in 30mL and 60mL bottles, may pose health risks. Consumers should contact Akorn for details.
AkornAug 13, 2021 - UnratedDrug
SigmaPharm Laboratories LLC recalls Sodium Phenylbutyrate POWDER, 250 grams bottle, Rx Only, Sigmapharm Laboratories, LLC Bensalem, PA 19020 NDC
SigmaPharm recalls specific batches of Sodium Phenylbutyrate powder (Rx only) due to failed impurities testing. Affected lots expire May 2023-Nov 2023. Consumers should contact the manufacturer for details.
SigmaPharmAug 13, 2021 - UnratedDrug
Pfizer Inc. recalls Chantix (varenicline) tablets 0.5mg, 56 Tablets, Rx only, Distributed by Pfizer Labs, Division of Pfizer Inc. NY, NY
Pfizer recalls Chantix 0.5mg tablets due to potential N-nitroso-varenicline impurity above FDA limits. Affected lots made in Ireland with specific NDC numbers.
PfizerAug 13, 2021 - UnratedDrug
First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy recalls PYRIDOXINE HCL (B6) 100MG/ML MDV, Red Mountain Compounding Rx
Red Mountain Compounding Pharmacy recalls all PYRIDOXINE HCL (B6) : FDA inspection raised sterility assurance concerns. No remedy specified in recall notice.
Red Mountain Compounding PharmacyAug 13, 2021 - UnratedFood
Hostess Brands, LLC recalls Hostess Soft White Hot Dog Buns, Net Wt. 12 OZ, UPC 888109110970
Hostess recalls Soft White Hot Dog Buns (12 oz) due to potential Listeria and Salmonella contamination. Consumers should avoid these products if they were purchased between August 2021 and September 2021.
HostessAug 13, 2021 - UnratedFood
Kansas City LLC., DBA Best Harvest Bakeries recalls Hotdog buns, in unlabeled clear plastic bags, 30 or 12 buns per bag.
Best Harvest Bakeries recalls hotdog buns in unlabeled clear plastic bags due to potential Listeria and Salmonella contamination. Consumers should check for the product and follow safety steps.
Best Harvest BakeriesAug 13, 2021 - Lower riskFood
Mai Cuisine recalls August Box of the Month NCA UPC: 84003140261 Products were sold from Genji Sushi counters inside Whole Foods Market
Mai Cuisine recalls August Box of the Month NCA (UPC 84003140261) sold at Whole Foods for Salmonella contamination in shrimp used in sushi.
Mai CuisineAug 13, 2021 - Lower riskFood
Sysco Atlanta, LLC recalls MINOR'S SEAFOOD BASE NO MSG GF 6/16 OZ (1 lb) 453 G UNITS Plastic container (pint) gluten free DISTRIBUTED BY NESTLE
Minor's gluten-free seafood base (6/16 oz) distributed by Nestle may be unsafe due to improper temperature storage. Recalled lots shipped between July 14 and August 13, 2021.
Minor'sAug 13, 2021 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2022) recall — Vehicle Speed Control
Daimler Trucks North America recalls 2022 Thomas Built Saf-T-Liner C2 school buses due to gas pedal misalignment causing unintended acceleration. Owners must contact DTNA for free repairs by February 5, 2022.
Thomas BuiltAug 12, 2021 - Use cautionVehicle
AUDI Q5 (2020) recall — Electrical System
Audi is recalling certain 2021-2022 Q5 models due to potential engine power loss from gateway control module shutdowns caused by liquid ingress. Owners must contact Audi for free repairs.
AudiAug 12, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system
GE Healthcare recalls Centricity Universal Viewer 7.0 software versions due to study changes not saving to archives. Affected units may experience data loss if images are modified.
GE HealthcareAug 12, 2021
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