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
35,004 found- Use cautionVehicle
HYUNDAI SONATA (2014) recall — Fuel System, Gasoline
Hyundai is recalling 2013-2014 Sonata vehicles with a potential fuel line crack that could cause fire. Owners must have fuel hose inspected and repaired free by dealers.
HyundaiFeb 28, 2020 - Use cautionVehicle
HYUNDAI SONATA (2020) recall — Equipment
Hyundai recalls 2020 Sonata vehicles with incorrect tire size labels that could lead to handling issues and crash risk. Owners will get free label updates by dealers.
HyundaiFeb 28, 2020 - Lower riskMedical device
Smiths Medical ASD Inc. recalls Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product Usage: Portex lumbar puncture trays provide
Smiths Medical recalls Portex Lumbar Puncture Tray model 4826PL-20 due to mislabeled inner trays. Affected units may have incorrect SKU numbers.
Smiths MedicalFeb 28, 2020 - Lower riskMedical device
CooperSurgical, Inc. recalls Wallace Artificial Insemination Catheter, 180 mm, Sterile, Quantity: 1 Box (10 units), Model: AIC18JP, Cooper Surgical
Cooper Surgical recalls 10-unit boxes of Wallace Artificial Insemination Catheters (Model AIC18JP) due to incorrect 5-year expiry date instead of 3-year safety expiry. This affects fertility treatments and requires immediate verification.
Cooper SurgicalFeb 28, 2020 - Lower riskMedical device
Abbott recalls Merlin PCS 3650 Software Upgrade Kit, REF 3330 St. Jude Medical The MerlinTM Patient Care System (MerlinTM PCS) Model
St. Jude Medical recalls Merlin PCS 3650 Software Upgrade Kit (REF 3330) due to potential incorrect energy settings during device programming, which may not alert users to retained values.
St. Jude MedicalFeb 28, 2020 - Stop using nowMedical device
Argo Medical Technologies Ltd recalls ReWalk Personal 6.0, ReWalk Personal 5.0 and ReWalk R Systems orthotically fits to the lower limbs and part of the
Argo Medical recalls ReWalk Personal 6.0, 5.0 and R Systems due to fire risk from waistpack lithium-ion batteries during charging. Affected users should contact for remedy.
Argo Medical TechnologiesFeb 28, 2020 - UnratedDrug
Sunstar Guangzhou Ltd. recalls Sunstar GUM Toothpaste 3 g tubes, Toothpaste made in Japan, packed in China, NDC 53050-0002-01
Sunstar Guangzhou Ltd. recalls specific lots of Sunstar GUM 3g toothpaste tubes due to current good manufacturing practice deviations.
Sunstar GUMFeb 28, 2020 - Lower riskFood
National Vitamin Company Inc recalls Nature's Blend Folic Acid 1000 mcg Dietary Supplement, 1000-count bottle, Product Number: 1280, UPC 0-79854-51280-9
National Vitamin Company Inc recalls Nature's Blend Folic Acid due to a label error stating 1000 mg instead of 1000 mcg. Check your bottle.
Nature's BlendFeb 28, 2020 - Lower riskFood
Domino Foods Inc recalls GREAT VALUE¿ Pure Granulated Sugar, 10 lbs. Sold as individual bags on a unitized 1/2 pallet 78 bags to a 1/2 pallet.
Domino Foods recalls 78 bags of Great Value Pure Granulated Sugar (10 lbs) due to possible metal pieces. Consumers should check lot code M0071B7 and best by date 02/10/2023.
Domino FoodsFeb 28, 2020 - Use cautionVehicle
KEYSTONE BULLET (2020) recall — Structure
Keystone is recalling certain 2020 Bullet 34RI RVs that may lack an emergency exit window, potentially delaying passenger evacuation during emergencies. Owners must have the window replaced free by dealers.
KeystoneFeb 27, 2020 - Use cautionVehicle
CHEVROLET SILVERADO 1500 (2020) recall — Service Brakes, Hydraulic
General Motors recalls 2020 Chevrolet Silverado 1500 vehicles with potentially unsafe brake caliper bolts that could break under load, increasing crash risk. Owners must contact GM for free replacement.
ChevroletFeb 27, 2020 - Use cautionMedical device
DeRoyal Industries Inc recalls DeRoyal SECURITY CUFFS, Single Strap, QR Buckle Cuff and Bed, UNIVERSAL, REF M8138 - Product Usage: patient restraint.
DeRoyal recalls security cuffs with a weak buckle that may not hold patients securely. Affected units have lot code 50192186. Contact for remedy.
DeRoyalFeb 27, 2020 - Lower riskMedical device
Shanghai United Imaging Healthcare Co., Ltd. recalls uDR 596i Digital Medical X-Ray Imaging System - Product Usage: intended to use by a qualified/ trained doctor or
Shanghai United Imaging Healthcare recalls uDR 596i X-Ray Systems with software versions R002.19.0-1.8402-690106 and R002.19.0.8648.690112 due to incorrect anatomical positioning and potential radiation exposure risks.
Shanghai United Imaging HealthcareFeb 27, 2020 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH 930 Analyzer, Siemens Material Number 11067000 with software version v1.21.0 SP1 or lower
Siemens Healthcare recalls Atellica CH 930 Analyzers with software version v1.21.0 SP1 or lower due to potential test result errors when editing assay definitions without saving. Affected units have serial numbers listed in the recall notice.
Siemens HealthcareFeb 27, 2020 - Use cautionMedical device
Smith & Nephew, Inc. recalls NAVIO Soft Tissue Protector, included in instrument kits. The NAVIO Tissue Protector is a reusable instrument designed
Smith & Nephew recalls NAVIO Soft Tissue Protectors in specific instrument kits due to potential bone pin sticking during surgery. Affected kits have listed lot numbers; contact for remedy.
Smith & NephewFeb 27, 2020 - Lower riskMedical device
Gentell, Inc recalls Gentell Hydrogel Ag 4x4, model no. GEN-11420 - Product Usage: Under the care of a healthcare professional, Gentell
Gentell Hydrogel Ag 4x4 (model GEN-11420) is recalled due to improper FDA registration. This product is used for wound care under healthcare supervision. Consumers should contact the manufacturer for details.
GentellFeb 27, 2020 - Lower riskMedical device
CME America LLC recalls CMEAmerica BodyGuard Wall Charger: Lot number 2019-0364, Mode/Catalogue number 151-143XL, *+B 01151143X
CME America recalls BodyGuard Wall Charger (Lot 2019-0364) due to risk of improper infusion pump battery charging. Affected units may not charge correctly, potentially causing medical issues.
CME AmericaFeb 27, 2020 - Lower riskDrug
The Harvard Drug Group recalls Quetiapine Fumarate Extended-Release Tablets, 150 mg, 100 tablets per unit dose carton, Rx only, Manufactured by: Lupin
The Harvard Drug Group recalls Quetiapine Fumarate Extended-Release Tablets due to incorrect package insert. This may cause confusion about proper use. Contact for details.
The Harvard Drug GroupFeb 27, 2020 - Stop using nowDrug
Pfizer Inc. recalls Elelyso (taliglucerase alfa) for injection, 200 units/vials,, Rx only, Distributed by Pfizer Labs, Division of Pfizer
Pfizer recalls Elelyso (taliglucerase alfa) injections after reports of loose metal ferrules causing potential contamination. Affected vials have specific lot numbers and expiration dates.
PfizerFeb 27, 2020 - Lower riskFood
Maryland Packaging, LTD. recalls Pure Cane Granulated Sugar, Single 10 lb. package, 156 paper bags on 2 1/2 CHEP pallets
Maryland Packaging recalls 10lb Pure Cane Granulated Sugar packages with possible metal wire foreign objects. Consumers should check product codes M0071A7 or M007:1B7 for affected items.
Maryland PackagingFeb 27, 2020 - UnratedFood
DANA USA Corp. recalls Sunshine Spice DRIED SHRI SKIN TRI TRI, Weight (lb) 0.215
DANA USA Corp. recalls Sunshine Spice Dried Shri Skin Tri Tri (0.215 lb) due to undeclared sulfites in product label. Consumers should check pack date and sell by date.
DANA USA Corp.Feb 27, 2020 - Lower riskFood
Snow's Acquisition, LLC recalls Barts Ice Cream Co. brand of Chocolate Chip Cookie Dough ice cream (Vanilla ice cream with chunks of cookie dough and
Barts Ice Cream Co. recalls Chocolate Chip Cookie Dough ice cream mislabeled as gluten-free but contains wheat flour. Products with UPC 048896100169 from 03/05/21 to 06/04/21 are affected.
Barts Ice Cream Co.Feb 27, 2020 - Stop using nowConsumer product
Whalen Recalls Bayside Furnishings 9-Piece Dining Sets Due to Fall Hazard; Sold Exclusively at Costco (Recall Alert)
Whalen recalls Bayside Furnishings 9-piece dining sets due to chairs breaking and causing fall hazards. Affected units sold exclusively at Costco; consumers must stop using and get refunds.
Bayside FurnishingsFeb 27, 2020 - Stop using nowConsumer product
Step2 Recalls Children's Grocery Shopping Carts Due to Laceration Hazard
Step2 recalls Little Helper's children's grocery shopping carts with specific model numbers and date codes due to risk of sharp basket pieces causing lacerations. Consumers should stop using and get a free replacement or $40 credit.
Step2Feb 27, 2020 - Use cautionConsumer product
Lennox Industries Recalls Ductless Heat Pumps Due to Fire Hazard
Lennox recalls three ductless heat pump models due to fire risk from overheating. Affected units must be replaced by a professional to prevent fire hazards.
LennoxFeb 27, 2020 - Use cautionConsumer product
Just Blanks Children's Nightgowns Recalled by Ishtex Textile Products Due to Violation of Federal Flammability Standard; Burn Hazard
Just Blanks children's nightgowns fail federal flammability standards, risking burns. Recalled items sold in 2019 with specific prints and sizes. Consumers should stop using and get refunds.
Just BlanksFeb 27, 2020 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2020) recall — Other
Daimler Trucks North America recalls 2017-2020 Thomas Built Buses Saf-T-Liner C2 school buses with faulty warning lights that could cause unsafe bus operations. Owners must contact DTNA for free updates.
Thomas Built BusesFeb 26, 2020 - Use cautionVehicle
NISSAN VERSA (2020) recall — Fuel System, Gasoline
Nissan is recalling 2020 Versa vehicles with a potential fuel leak risk if tank filled over half full, which could cause fire. Owners will get free fuel tank replacements.
NissanFeb 26, 2020 - Use cautionMedical device
Philips North America, LLC recalls HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4,
Philips recalls HeartStart MRx Defibrillators with specific model numbers due to risk of device failure after being dropped or hit, potentially leading to patient death.
PhilipsFeb 26, 2020 - Lower riskMedical device
Capso Vision, Inc. recalls The CapsoCam Plus (SV-3); Device Common Name: System, Imaging, Gastrointestinal, Wireless, Capsule; Catalog Number 2795
Capso Vision recalls The CapsoCam Plus (SV-3) capsules due to incorrect capture mode causing data recording failure. This may lead to delayed diagnosis and repeat exams. Affected units have specific serial numbers and lot numbers.
CapsoFeb 26, 2020
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,592 recalls tracked · 72,039 explained in plain English · 10,976 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.