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
35,021 found- Use cautionVehicle
ENTEGRA QWEST (2020) recall — Electrical System
Jayco is recalling certain 2020-2021 Entegra Qwest motorhomes with swivel seats due to potential wiring harness damage causing airbag deployment issues. Owners should contact Jayco for free repairs.
JaycoOct 8, 2020 - Use cautionMedical device
Medicrea International recalls MEDICREA LIGAPASS TENSION PULLEY HANDLE XS- intended to provide thoracic and/or lumbar posterior stabilization for
Medicrea recalls LIGAPASS Tension Pulley Handle XS- for potential band breakage during surgery, risking infection and reoperation. Affected units have specific lot numbers and were sold from 2017-2019.
MedicreaOct 8, 2020 - Lower riskMedical device
Microbiologics Inc recalls KWIK-STIK(TM) 2 Pack Clostridium perfringens derived from ATCC(R) 13124(TM)
Microbiolog: KWIK-STIK 2-Pack with incorrect lot number 218-234-4 printed on foil pouch. Recalled due to misprint risk of using wrong lot number.
MicrobiologicsOct 8, 2020 - UnratedMedical device
Microbiologics Inc recalls Each KWIK-STIK unit contains a lyophilized microorganism pellet, an ampoule of hydrating fluid, and an inoculating
Microbiolog: KWIK-STIK 6-pack units may contain NDM-1 negative Klebsiella pneumoniae instead of NDM-1 positive strain. This could lead to ineffective treatment for certain infections. Affected units have specific catalog and lot numbers.
MicrobiologicsOct 8, 2020 - Lower riskMedical device
RAYSEARCH LABORATORIES AB recalls RayStation standalone software treatment planning system, Model No. 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3, 7.0,
RaySearch recalls specific software versions for radiation therapy planning due to potential incorrect reference links in imported treatment plans. Affected users should check version numbers and contact RaySearch for guidance.
RaySearchOct 8, 2020 - Lower riskMedical device
Microbiologics Inc recalls Catalog 02145P, Klebsiella pneumoniae derived from NCTC 13439 - Product Usage: intended to be used as controls to
Microbiologics recalls Catalog 02145P bacterial controls for microbial testing due to incorrect VIM-1 status. These controls may not verify assay performance properly.
MicrobiologicsOct 8, 2020 - Use cautionMedical device
Enterix, Inc. recalls InSure ONE Test Strips (25 pack) vials-fecal immunochemical test (FIT) qualitatively detects human hemoglobin from
Enterix, Inc. recalls InSure ONE Test Strips due to potential false positive results. Check lot numbers 770G11 and 770G21 for details.
InSure ONEOct 8, 2020 - Use cautionMedical device
Canon Medical System, USA, INC. recalls CAS-930A Flat Panel Monitor (FPD) used in conjunction with the Canon Interventional Angiography System, Model numbers:
Canon Medical recalls CAS-930A Flat Panel Monitors used with Infinix-8000C/H systems due to potential cable breakage during procedures, risking patient vessel damage.
Canon MedicalOct 8, 2020 - Lower riskDrug
Denton Pharma, Inc. recalls Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, a) 30 count (NDC 70934-309-30); b) 60 count (NDC
Denton Pharma recalls Metformin Hydrochloride Extended-Release Tablets (500mg) due to detected N-Nitrosodimethylamine (NDMA) impurity above safe levels. Affected products include 30-count, 60-count, 90-count, and 120-count bottles with specific NDC numbers and expiration dates.
Denton PharmaOct 8, 2020 - Stop using nowFood
High Quality Organics recalls Vox Spice, Allegro Coffee Company Organic White Wine Shallot Seasoning; Food Service 90 oz.PET jar; 4 jars per case
High Quality Organics recalls Vox Spice Organic White Wine Shallot Seasoning due to confirmed Salmonella. Check lot numbers and best-by dates.
Vox SpiceOct 8, 2020 - Lower riskMedical device
Steris Corporation recalls Olympus Leak Test Adapter used with Acu-sInQ Complete Endoscope Cleaning Aid Systems-intended to assist manual flexible
Steris recalls Olympus Leak Test Adapter used with Acu-sInQ endoscope cleaning systems due to potential cleaning solution intrusion into endoscopes. Affected units distributed from May 2017 to June 2020.
SterisOct 7, 2020 - Stop using nowDrug
Baxter Healthcare Corporation recalls Bupivacaine Hydrochloride in 8.25% Dextrose Injection, USP Spinal 0.75% (15 mg/2 mL) 10 x 2 mL single-dose ampules, Rx
Baxter Healthcare recalls spinal anesthetic ampules with black and transparent particles. Stop using if you have these specific lots. No remedy provided in official notice.
BaxterOct 7, 2020 - Use cautionConsumer product
Prestone Products Recalls Antifreeze Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Poisoning
Prestone antifreeze products with specific model numbers and date codes were recalled due to child-resistant packaging failure, posing poisoning risk if swallowed by young children.
PrestoneOct 7, 2020 - Use cautionConsumer product
Harbor Breeze Kingsbury Ceiling Fans Recalled by HKC-US Due to Impact and Laceration Injury Hazards; Sold Exclusively at Lowe's Stores
Harbor Breeze Kingsbury ceiling fans made before Dec 2018 recalled due to light globe falling and causing laceration injuries. Consumers need new owner's manual and light kit label for safe installation.
Harbor B: KingsburyOct 7, 2020 - Stop using nowConsumer product
Endliss Technology Recalls Trianium Battery Phone Cases Due to Burn Hazard; Sold Exclusively on Amazon.com
Endliss Technology recalls Trianium battery phone cases sold on Amazon due to risk of overheating batteries causing burns. Consumers must stop using and dispose of recalled cases.
Endliss TechnologyOct 7, 2020 - Stop using nowConsumer product
CB2 Recalls Bordo Dining Tables Due to Injury Hazard
CB2 recalls Bordo and Bordo XL concrete dining tables due to risk of collapse when moved, causing injury. Affected models include white tables with specific dimensions and SKUs. Consumers should stop using and get a refund.
CB2Oct 7, 2020 - Use cautionVehicle
KME PREDATOR (2014) recall — Service Brakes
KME is recalling 2014 Predator vehicles with Telma induction braking systems due to risk of brake retarder separating during use. Owners must have hardware inspected and replaced by dealers.
KMEOct 6, 2020 - Use cautionVehicle
GILLIG LOW FLOOR (2019) recall — Suspension
Gillig is recalling certain 2018-2020 Low Floor buses due to potential rear suspension failure causing reduced handling and stability. Owners will receive free new control rods with improved bushings.
GilligOct 6, 2020 - Use cautionMedical device
Arjohuntleigh Magog, Inc. recalls Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slings is designed
Arjohuntleigh Magog recalls Flat Dynamic Positioning Systems used with passive clip slings due to risk of sling clip breakage during resident transfers in homecare settings.
Arjohuntleigh MagogOct 6, 2020 - Lower riskMedical device
Exactech, Inc. recalls Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium
Exactech recalls specific model Equinoxe Cage Glenoid implants due to potential mislabeling. Affected units include serial numbers listed in the recall notice. Consumers should verify their product against the provided list.
ExactechOct 6, 2020 - Lower riskMedical device
Hardy Diagnostics recalls Strep B Carrot Broth One-Step, Ref. Z40, UDI: 00819398026499
Hardy Diagnostics recalls Strep B Carrot Broth One-Step (Ref. Z40) due to incorrect expiration date on culture medium packaging. The label shows 2021-11-10 instead of the correct 2020-11-10. Consumers should check their product's expiration date and contact Hardy Diagnostics for details.
Hardy DiagnosticsOct 6, 2020 - Lower riskDrug
PD-Rx Pharmaceuticals, Inc. recalls metformin HCL ER 750 mg Rx only Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 30 tablets NDC:
PD-Rx Pharmaceuticals recalls metformin HCl ER 750mg tablets with N-Nitrosodimethylamine (NDMA) impurity above safe levels. Affected lots expire through March 2022. Consumers should stop using and contact for return.
PD-RxOct 6, 2020 - Use cautionDrug
eVenus Pharmaceutical Laboratories recalls Desflurane, USP Liquid for Inhalation, 240 mL, Rx Only, Manufactured by: Shanghai Hengrui Pharmaceutical Co., Ltd.,
eVenus Pharmaceutical Laboratories recalls Desflurane 240mL inhalation liquid due to leaking container risk. This prescription drug may cause injury if used improperly. Contact for return instructions.
eVenus Pharmaceutical LaboratoriesOct 6, 2020 - Lower riskFood
WOLFGANG CONFECTIONERS recalls Hu Cashew Hunks, Hu Cashews + Vanilla Bean Chocolate Covered Hunks 4 oz., stand up pouch, 6 bags per case .
Wolfgang Confectioners recalls Hu Cashew Hunks and Hu Cashews pouches due to mislabeling: cashews found in almond product pouches. Consumers should check UPC 850180006473 and lot 202183.
Wolfgang ConfectionersOct 6, 2020 - Lower riskFood
Ariola Foods Corp. recalls Frozen raw Lobster Tail pastry 100 count, sold in 15LB, 24LB, 40.25LB cases
Ariola Foods recalls frozen lobster tail pastry due to undeclared wheat and food dyes. Consumers should check UPCs and use within 3 months.
Ariola FoodsOct 6, 2020 - Lower riskMedical device
Bayer Medical Care, Inc. recalls Brand Name: MEDRAD Stellant FLEX Syringe Kits Common Name: Angiographic Syringe Catalog/REF Number: FLEXD-150-SCS
Bayer Medical Care recalls specific lots of MEDRAD Stellant FLEX 150 mL syringe kits that may have holes or cracks causing fluid leaks. Affected units include lot numbers 8584324-8586388 and 8585234. Consumers should check their syringes for damage and contact Bayer for details.
MEDRADOct 5, 2020 - Lower riskMedical device
Becton, Dickinson and Company, BD Biosciences recalls BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Usage: intended as a complete process control for
BD Biosciences recalls Multi-Check CD4 Low Control 2.5mL IVD due to potential inaccurate results from unexpected cell population dim CD3 expression. Affected lots include BM1020L and others.
BD BiosciencesOct 5, 2020 - Lower riskMedical device
Thera Test Laboratories, Inc. recalls EL-Anti-SARS-CoV-2 IgG Kit, Catalog #104-130. Submitted as EUA202128
Thera Test recalls EL-Anti-SARS-CoV-2 IgG Kit (Catalog #104-130) due to potential false positives. Affected lots expire May 2021.
Thera TestOct 5, 2020 - Lower riskMedical device
Tytek Medical Inc recalls TyTek Tension Pneumothorax Access Kit TPAK 14 gauge 3.25 inch- Intended for introduction into the body to facilitate
Tytek Medical recalls TPAK 14 gauge kits made before Oct 5, 2020 due to updated safety instructions for needle decompression procedures.
Tytek MedicalOct 5, 2020 - Lower riskMedical device
Micro-Tech Usa recalls Elastic Traction Device, 11mm Lower. UPN: ER56041 Reference Number: ETD-D-26-235-C-N - Product Usage: indicated for use
Micro-Tech recalls Elastic Traction Devices (11mm Lower) due to FDA classification requirements. The device requires 510(k) clearance for US market but was not appropriately classified as Class I.
Micro-TechOct 5, 2020
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,609 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.