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- Lower riskDrug
Hikma Pharmaceuticals USA Inc. recalls Bleomycin for Injection, USP, packaged in 15 units per single dose vial, Rx only, Manufactured by Thymoorgan Pharmazie
Hikma Pharmaceuticals recalls Bleomycin injection vials due to mislabeling. This may affect patients using prescription cancer treatment. Contact Hikma for details.
HikmaAug 5, 2021 - Use cautionVehicle
CHEVROLET TAHOE (2016) recall — Seat Belts
General Motors recalls 2016 Chevrolet Tahoes with potentially faulty seat belt pretensioner cables that could reduce effectiveness and increase injury risk during crashes. Owners must have the cable replaced free by dealers.
ChevroletAug 4, 2021 - Use cautionVehicle
CHEVROLET TRAVERSE (2019) recall — Air Bags
Chevrolet is recalling 2019 Traverse vehicles with unsecured side curtain air bags that may not deploy properly, increasing injury risk. Owners must have their air bags inspected by dealers for free.
ChevroletAug 4, 2021 - Use cautionVehicle
JAGUAR XE (2020) recall — Structure
Jaguar recalls 2020 XE vehicles with weakened rear rail assembly that may detach when towing, increasing crash risk. Owners receive free replacement.
JaguarAug 4, 2021 - Stop using nowMedical device
Mac Medical Supply Co Inc recalls Ultrasound Gel labeled under the following brand names: MediChoice Ultrasound Gel, Athena Liquasonic Ultrasound Gel,
Mac Medical Supply recalls ultrasound gels with bacterial contamination risk. Products sold between August 2018 and August 2021 may contain harmful bacteria. Consumers should stop using affected items immediately.
Mac Medical SupplyAug 4, 2021 - Lower riskMedical device
Smiths Medical ASD Inc. recalls smiths medical portex Tracheal Intubation Stylet, REF 100/120/200, 4.0mm OD X 335mm, 10/box, sterile.
Smiths Medical recalls sterile tracheal intubation stylets with incorrect device in package. Consumers should check product details and contact Smiths Medical for guidance.
Smiths MedicalAug 4, 2021 - Lower riskMedical device
Abbott Molecular, Inc. recalls Vysis CLL FISH Probe Kit with the following components: Vysis LSI p53 SpectrumOrange/ATM, SpectrumGreen and LSI
Abbott recalls Vysis CLL FISH Probe Kits that may not detect 13q deletions in cancer samples. Affected kits have specific part numbers and lot codes. Contact Abbott for details.
AbbottAug 4, 2021 - Lower riskMedical device
Roche Molecular Systems, Inc. recalls cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System, Catalog Number 09211101190
Roche recalls cobas SARS-CoV-2 & Influenza A/B Test for false positive results. Affected units have Catalog Number 09211101190 and Lot 10119Z.
RocheAug 4, 2021 - Lower riskMedical device
Cardinal Health recalls Monoject 0.9% Sodium Chloride Flush Syringe, 5mL Fill, STERILE, Product Code 8881570125 The proposed device is
Cardinal Health recalls Monoject 0.9% Sodium Chloride Flush Syringes due to potential air reintroduction after expelling air. Affected units have specific product codes and were sold in certain regions.
Cardinal HealthAug 4, 2021 - Lower riskFood
Molly and Me Pecans recalls MOLLY & ME PECANS all natural PRALINE PECANS, 4 oz., 7 oz., and 12 oz packages, INGREDIENTS: Pecans, Brown Sugar,
Molly and Me Pecans is recalling all natural praline pecans due to undeclared soy in the product. This may pose a risk for people with soy allergies.
Molly and Me PecansAug 4, 2021 - Lower riskFood
OLAM Edible Nuts-Blakely,GA recalls Raw Shelled Peanuts, Skins Removed, Split Nut Blanched Runner Peanuts, Net. Wt. 2000# Olam Edible Nuts - Blakely, GA
OLAM Edible Nuts recalls raw shelled peanuts with metal objects. Consumers should check lot numbers and contact the company for details.
OLAM Edible NutsAug 4, 2021 - Lower riskFood
DSD Merchandisers, Inc. recalls Dark Chocolate Malt Balls in plastic container; 9 oz./ 255g UPC: 6 5143370179 0 Packed on the same equipment as
DSD Merchandisers recalls Dark Chocolate Malt Balls (UPC 651433701790) due to undeclared peanuts. Consumers may have purchased this product with milk, eggs, tree nuts, peanuts, wheat, or soy.
DSD MerchandisersAug 4, 2021 - Stop using nowConsumer product
Two Million Dehumidifiers With Well-Known Brand Names Recalled Due to Fire and Burn Hazards; Manufactured by New Widetech
Recall of 25-74 pint dehumidifiers from brands like AeonAir, Danby, and Whirlpool due to fire and burn hazards. Stop using immediately and get a refund based on age.
New WidetechAug 4, 2021 - Stop using nowConsumer product
Sling Loungers Sold at Dollar General Recalled Due to Amputation, Laceration, and Pinching Hazard; Manufactured by Shanghai Worth Garden Products
Recalled True Living Sling Loungers (2019) can collapse unexpectedly, causing amputation, laceration, or pinching if fingers get caught in metal folding joints. Stop using immediately and return for refund.
True LivingAug 4, 2021 - Use cautionConsumer product
LG Energy Solution Michigan Recalls Home Energy Storage Batteries Due to Fire Hazard
LG Energy Solution Michigan recalls RESU10H lithium-ion home batteries due to fire risk from overheating. Owners must contact for free replacement before the batteries overheat.
LG Energy Solution MichiganAug 4, 2021 - Use cautionVehicle
FOREST RIVER CARDINAL (2021) recall — Equipment
Forest River recalls 2021 Cardinal fifth wheels due to potential spare tire carrier detachment causing crash risk. Owners must contact customer service for free fix.
Forest RiverAug 3, 2021 - Lower riskMedical device
Luminex Corporation recalls Verigene EP Amplification Reagent Kit Test
Luminex recalls Verigene EP Amplification Reagent Kit Test with potential for false positive results. Affected lots include specific model numbers and dates. Consumers should check their kit's lot number and contact Luminex for details.
LuminexAug 3, 2021 - Lower riskMedical device
Fresenius Medical Care Holdings, Inc. recalls AquaBplus Water Purification System, Part Number 24-2000-0, AquaBplus 2500 - Typ USA (G02040108-US), AquaBplus 2000 -
Fresenius Medical Care recalls AquaBplus 2000/2500 water purifiers due to installation error risk. The US installation guide incorrectly allowed 3-ring mains instead of 2-ring, potentially reducing disinfection effectiveness.
Fresenius Medical CareAug 3, 2021 - Stop using nowMedical device
Olympus Corporation of the Americas recalls Arc Endocuff Vision as follows: ARV110 ENDOCUFF-V M BLUE PK8, Part Number: E0420501; ARV120 ENDOCUFF-V L GREEN PK8,
Olympus recalls Arc Endocuff Vision devices with packaging seal defects that may allow bacterial contamination and patient infection. Affected models include specific sizes and lot numbers.
OlympusAug 3, 2021 - UnratedDrug
Teligent Pharma, Inc. recalls Lidocaine Hydrochloride Topical Solution, USP, 4% , 50 mL glass bottles, Rx Only, Teligent Pharma Inc. Buena, New
Teligent Pharma recalls 4% Lidocaine Hydrochloride Topical Solution (50mL glass bottles) due to superpotent drug risk. Rx-only product with specific lot numbers and expiration date.
Teligent PharmaAug 3, 2021 - UnratedDrug
The Harvard Drug Group recalls Fexofenadine Hydrochloride Tablets, 60 mg, 500 Tablets per bottle, Distributed by: Major Pharmaceuticals, 17177 N.
Harvard Drug Group recalls 60mg fexofenadine tablets with impurities that could pose health risks. Affected lots expired by April 2022. Consumers should check NDC 0904-6979-40 and lot numbers.
The Harvard Drug GroupAug 3, 2021 - Lower riskFood
Cocanu LLC recalls Moonwalk 70% dark chocolate bar. It is packaged in white shiny paper with blue print. Net Weight: 1.2 oz / 35gr. No
Moonwalk 70% dark chocolate bars with lactose in ingredients but not declared on label are being recalled. This may affect consumers with lactose intolerance.
MoonwalkAug 3, 2021 - Use cautionVehicle
BMW K 1600 GTL (2014) recall — Fuel System, Gasoline
BMW is recalling 2014 K 1600 GTL motorcycles due to a fuel pump that may crack and leak fuel, creating fire risk if near ignition sources.
BMWAug 2, 2021 - Use cautionVehicle
PJ TRAILERS UC (2021) recall — Suspension
PJ Trailers is recalling 2021 C4, C5, U8, UL, U6, and UC trailers with missing inner bearings that could cause wheel separation and crashes.
PJ TrailersAug 2, 2021 - Lower riskMedical device
Magnolia Medical Technologies, Inc. recalls Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access
Magnolia Medical recalls Steripath Luer Transport Pack Gen2 due to incorrect transfer adapter instructions. This may lead to improper specimen handling. Affected units include specific catalog and lot numbers.
Magnolia MedicalAug 2, 2021 - Use cautionMedical device
GE Healthcare, LLC recalls Flow sensors that may be installed in the following GEHC anesthesia machines: (1) Aestiva MRI, GTIN 0080682102339; (2)
GE Healthcare recalls flow sensors installed in certain anesthesia machines made before June 2021. These sensors may cause leaks leading to incorrect anesthesia dosing. Affected models include Aestiva MRI, Aestiva 7900, and others.
GE HealthcareAug 2, 2021 - Lower riskMedical device
Shanghai United Imaging Healthcare Co., Ltd. recalls uEXPLORER PET/CT System - Product Usage: intended to be operated by qualified healthcare professionals to assist in the
Shanghai United Imaging Healthcare recalls uEXPLORER PET/CT systems due to occasional workflow freezes after canceling PET scans. Affected units may require professional evaluation.
Shanghai United Imaging HealthcareAug 2, 2021 - Lower riskMedical device
CAREFUSION recalls BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV, REF: 10037031; BD Gravity
CAREFUSION recalls Gravity Burette Sets with potential flow problems that could delay medical therapy. Affected models include 60-drop sets with specific serial numbers. Contact CAREFUSION for details.
CAREFUSIONAug 2, 2021 - Lower riskDrug
Macleods Pharma Usa Inc recalls Clopidogrel Tablets, USP, 75 mg, 500-count bottle, Rx only, Manufactured for: Macleods Pharma USA, Inc., Plainsboro, NJ
Macleods Pharma USA recalls 75mg Clopidogrel tablets due to foreign matter. Rx-only 500-count bottles with specific lot number and expiration date.
MacleodsAug 2, 2021 - UnratedDrug
Akorn, Inc. recalls Artificial Tears Ointment, Lubricant Eye Ointment, Net Wt. 3.5 g (1/8 oz.) per tube, Sterile, Manufactured by: Akorn,
Akorn recalls sterile eye ointment due to non-sterility issues found during stability testing. Products may contain harmful bacteria from Bacillus cereus group. Affected lots expire June 2022 through September 2022.
AkornAug 2, 2021
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- October 2026 recall report
- All monthly reports
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.