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
35,006 found- Stop using nowConsumer product
Costway Recalls Baby Strollers Due to Violation of Federal Stroller and Carriage Safety Standard; Fall, Entrapment and Strangulation Hazards (Recall Alert)
Costway recalls double strollers due to entrapment and strangulation risks. Stop using immediately and contact Costway for a full refund.
CostwayJun 25, 2020 - Use cautionVehicle
TOYOTA PRIUS V (2017) recall — Hybrid Propulsion System
Toyota recalls 2017 Prius V vehicles with potential hybrid system shutdown causing stalling. Free software update and inverter repair available to prevent crashes.
ToyotaJun 24, 2020 - Lower riskVehicle
VOLKSWAGEN GOLF (2018) recall — Equipment
Volkswagen recalls two 2018 Golf GTI vehicles with potential VIN mismatch on certification labels, risking crashes or fires. Owners must get a corrected label installed.
VolkswagenJun 24, 2020 - Use cautionVehicle
TOYOTA RAV4 (2020) recall — Steering
Toyota recalls 2019-2020 RAV4 and Hybrid models with electric power steering due to potential water entry causing loss of steering assist. Owners must have gear box replaced free by dealers.
ToyotaJun 24, 2020 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls syngo.via RT Image Suite with software versions syngo.via VB30 or VB40
Siemens recalls syngo.via RT Image Suite software versions VB30/VB40 due to rare image orientation errors that could lead to incorrect radiation treatment plans if not noticed.
SiemensJun 24, 2020 - Lower riskMedical device
Arthrex, Inc. recalls Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S - Product Usage: is intended to be used as a
Arthrex recalls titanium screws that are 5mm shorter than labeled, potentially causing improper bone fixation. Affected products include specific part numbers for orthopedic surgery.
ArthrexJun 24, 2020 - Use cautionMedical device
Smith & Nephew, Inc. recalls Smith & Nephew T-F1X0 RCG Drill Pac, 2 mm Drill & (2) Sleeves - Product Usage: indicated for use in surgical
Smith & Nephew recalls surgical drill packs with one sleeve instead of two, risking improper bone tunnel drilling during rotator cuff repairs. Affected units include specific lot numbers from August 2023.
Smith & NephewJun 24, 2020 - Lower riskMedical device
Smith & Nephew, Inc. recalls SUTUREFIX ULTRA Suture, Product number 72203855
Smith & Nephew recalls SUTUREFIX ULTRA Suture (product 72203855) due to packaging error sending XL drill instead of S drill. This longer drill may cause injury during use.
Smith & NephewJun 24, 2020 - Lower riskMedical device
DNA Genotek Inc. recalls PrepIT Q2A Kit, Model PT-Q2A-96 containing component reagent AG (PT-QAG-96) 1.4mL and ST (PT-QST-96) 2.9mL - Product
DNA Genotek recalls PrepIT Q2A Kit (Model PT-Q2A-96) due to reagents shipped after their use-by date. This may cause inaccurate results if used after expiration.
DNA GenotekJun 24, 2020 - UnratedMedical device
Smith & Nephew, Inc. recalls TRIGEN, Intramedullary nail - Product Usage: is intended to provide resistance for screw back-out. It provides
Smith & Nephew recalls TRIGEN intramedullary nails with a manufacturing error causing improper re-sterilization of the UHMWPE sleeve. Affected models include 71655139 lot 19BM13592A.
Smith & NephewJun 24, 2020 - Lower riskDrug
Medichem S.A. recalls Chlorhexidine Gluconate 0012 For Manufacturing, Processing or Repacking, RX Only, Medichem, S.A. Poligono Industrial
Medichem recalls Chlorhexidine Gluconate 0012 (RX only) due to microbial contamination with Serratia marcescens in some batches. This may pose health risks if used improperly.
MedichemJun 24, 2020 - Stop using nowFood
Beyond Better Foods Llc recalls Enlightened Dairy-Free Chocolate Peanut Butter Frozen Dessert, one Pint (473 ml). Case GTIN: 1-08-52109-33106-9. Item
Beyond Better Foods recalls Enlightened Dairy-Free Chocolate Peanut Butter Frozen Dessert pints due to undeclared milk. Check your freezer for the specific lot.
EnlightenedJun 24, 2020 - Lower riskFood
Whole Foods Market recalls Whole Foods Market Red Velvet Layered Cheesecake Slice PLU: 78620 packaged in plastic clam shell with scale label
Whole Foods Market recalls Red Velvet Layered Cheesecake Slice (PLU 78620) due to undeclared walnuts. Consumers should check packaging for sell-by dates through July 2020.
Whole Foods MarketJun 24, 2020 - Stop using nowFood
BUILT BRANDS LLC recalls Banana Chocolate Creme Chocolate covered protein bars, packaged in metalized polypropylene wrappers, packed in 6 count
Built Brands LLC recalls banana chocolate creme protein bars due to potential mold contamination before the expiration date.
Built BrandsJun 24, 2020 - Stop using nowConsumer product
The Furniture Connexion Recalls Modavari Forrest Live Edge Benches Due to Fall and Injury Hazards
Furniture Connexion recalls Modavari Forrest Live Edge Benches (model LE6) due to tipping risk. Consumers must stop using and contact for free repair kit.
Furniture ConnexionJun 24, 2020 - Use cautionVehicle
FORD F-550 SD (2020) recall — Power Train
Ford is recalling 2020 F-550 Super Duty trucks with a transmission issue that may cause engine stalling or increased braking effort, risking crashes. Owners must contact Ford for free transmission replacement.
FordJun 23, 2020 - Use cautionVehicle
FORD EXPEDITION (2020) recall — Seats
Ford is recalling 2020 Expedition vehicles with potentially weak seat headrest brackets that may not restrain occupants during crashes, increasing injury risk. Owners should contact Ford for free seat inspections.
FordJun 23, 2020 - Lower riskMedical device
Sutter Medizintechnik GmbH recalls Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re electrosurgical instruments. The bipolar for-ceps
Sutter recalls specific models of single-use electrosurgical forceps due to incorrect sterilization labeling in package inserts. The error could lead to improper sterilization methods.
SutterJun 23, 2020 - Lower riskMedical device
The Magstim Company Limited recalls Neurosign V4 Intraoperative Nerve monitor family of devices.
Magstim recalls Neurosign V4 nerve monitors with serial numbers 001-049 due to potential cable damage from improper handling. Affected units may require repair or replacement.
MagstimJun 23, 2020 - Use cautionMedical device
Chengdu Ai Qin E-commerce Co., Ltd recalls TTDEYE (brand) Radial Brown, B16112109 - Product Usage: Colored contact lenses
Chengdu Ai Qin E-commerce Co. recalls TTDEYE Radial Brown colored contact lenses distributed without FDA clearance. Check your product details.
TTDEYEJun 23, 2020 - Use cautionMedical device
Mevion Medical Systems, Inc. recalls MEVION S250 Proton Radiation Treatment System; intended to deliver proton radiation treatment to patients
Mevion recalls S250 proton radiation treatment systems with a sharp screen edge that could injure service technicians during maintenance. Affected units have specific lot numbers and UDI codes.
MevionJun 23, 2020 - UnratedDrug
VistaPharm, Inc. recalls Nystatin Oral Suspension, USP 500,000 units/5mL Cup, Delivers 5 mL, Rx Only, Manufactured by: VistaPharm, Largo, FL
VistaPharm recalls Nystatin Oral Suspension due to impurities exceeding safety limits. This may cause serious harm if used. Check your product's NDC or lot number for affected batches.
VistaPharmJun 23, 2020 - Stop using nowDrug
CareFusion 213, LLC recalls ChloraPrep With Tint (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)) 3 mL applicators -
CareFusion recalls 25-pack of ChloraPrep With Tint 3mL applicators due to Aspergillus Penicilloides contamination. Stop using if you have these items.
CareFusionJun 23, 2020 - Lower riskDrug
Biogen MA Inc. recalls Tecfidera (dimethyl fumarate) delayed-release capsules, 240 mg, 60-count bottle, Rx only, Manufactured by: Biogen Inc.,
Biogen recalls Tecfidera 240mg capsules due to a manufacturing issue that may have led to contaminated product distribution. Affected lots were distributed despite in-process rejection.
BiogenJun 23, 2020 - Stop using nowDrug
Itech 361 LLC recalls All Clean Hand Sanitizer, Fresh Scent, 1 Liter bottles, Ethyl Alcohol 70.00%, Produced by Eskbiochem SA de CV Ave
All Clean Hand Sanitizer (1L, Fresh Scent) contains undeclared methanol. Recalled due to chemical contamination risk. Consumers should stop using immediately.
All CleanJun 23, 2020 - Lower riskFood
Power Selles Imports dba Culinary Collective recalls Blanxart 85% Nicaragua Organic Dark Chocolate Bar, packaged in paper packaging with internal foil wrapper. Net weight
Culinary Collective recalls Blanxart 85% Nicaragua Organic Dark Chocolate Bar after a consumer found a foreign object in the product. The recall affects specific lot numbers and dates.
Culinary CollectiveJun 23, 2020 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Software versions syngo.CT VB20 or VB20_SP1 in the following systems: SOMATOM Force (Model #10742326) SOMATOM
Siemens recalls software versions syngo.CT VB20 and VB20_SP1 for certain CT scanners, which may cause workflow interruptions and delays in diagnosis due to unexpected notifications.
SiemensJun 22, 2020 - Use cautionMedical device
GE Healthcare, LLC recalls CARESCAPE ONE, Physiological Patient Monitor - Product Usage: is both a multi-parameter physiological patient monitor
GE Healthcare recalls CARESCAPE ONE patient monitors that may fail to alert for ventricular fibrillation when docked to specific host monitors, posing a risk of undetected cardiac events.
GE HealthcareJun 22, 2020 - Lower riskMedical device
Biosense Webster (israel), Ltd. recalls CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module - Product Usage: FGThe intended use of the system is
Biosense Webster recalls CARTO 3 System software version V7.1.80 due to rare risk of cardiac perforation from software defects during ablation procedures.
Biosense WebsterJun 22, 2020 - Stop using nowDrug
UVT INC recalls Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by
UVT INC recalls Saniderm Advanced Hand Sanitizer (1L) due to undeclared methanol. Consumers should stop using affected products to avoid chemical contamination risks.
UVT INCJun 22, 2020
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