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 cautionMeat & poultry
Central Valley Meat Co., Inc. Recalls Ground Beef Products Due to Possible Salmonella Dublin Contamination
Central Valley Meat Co. recalls Stater Bros ground beef products from July 2019 due to possible Salmonella Dublin contamination. Consumers should not consume recalled items and dispose of them safely.
Stater BrosNov 15, 2019 - Use cautionVehicle
FIAT 500 (2013) recall — Power Train
Chrysler recalls certain 2012-2013 Fiat 500s with 6-speed automatic transmissions due to shifter cable detachment risk. This may cause transmission failure or vehicle rolling away when in PARK, increasing crash risk. Owners must contact Chrysler for free shifter cable replacement.
ChryslerNov 15, 2019 - Use cautionVehicle
RAM PROMASTER (2018) recall — Equipment
Chrysler recalls certain 2015-2018 Ram ProMaster vehicles with overheating fan motors that could cause fire. Owners will receive free replacement of the cooling fan module.
ChryslerNov 15, 2019 - Use cautionVehicle
TRIUMPH SPEED TRIPLE RS (2019) recall — Power Train
Triumph recalls 2019 Speed Triple RS motorcycles with a potential gear shift issue that could cause missed gears or false neutral, increasing crash risk. Owners must contact Triumph for free replacement of the linkage clamp assembly.
TriumphNov 15, 2019 - Lower riskMedical device
Medtronic Navigation, Inc.-Littleton recalls O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000
Medtronic recalls specific O-arm O2 Imaging Systems due to a potential gantry belt loosening that could cause 3D images to rotate relative to patient position. Affected units have unique serial numbers and product codes.
MedtronicNov 15, 2019 - Lower riskMedical device
Tosoh Smd Inc recalls AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment of calibrators/controls. Part Number: 020706
Tosoh recalls AIA-PACK B12 Pretreatment Sets for diagnostic use due to potential barcode reading errors that may delay test results. Affected products include specific lot numbers with expiration dates.
TosohNov 15, 2019 - UnratedMedical device
Baxter Healthcare Corporation recalls Revaclear Capillary Dialyzer 300, REF Revaclear 300 Product Code 114745L
Baxter Healthcare recalls Revaclear 300 Dialyzer units with specific lot numbers due to potential presence of contaminants in header caps. Affected units may pose health risks requiring immediate action.
Baxter HealthcareNov 15, 2019 - Stop using nowMedical device
Arrow International Inc recalls Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J
Arrow recalls 60cm angiographic catheters with potential balloon extension line leaks that could cause slow deflation or contrast injection into vascular tissue, risking serious injury or death.
ArrowNov 15, 2019 - UnratedMedical device
Tytek Medical Inc recalls PneumoDart, 14 ga x 3.25in., REF TM-317 A compact, sterile, device intended for the introduction into the body to
Tytek Medical recalls PneumoDart 14-gauge needles due to a defect that may cause occlusion during use. Affected units were sold with specific lot numbers and expiration dates.
Tytek MedicalNov 15, 2019 - Lower riskDrug
Glenmark Pharmaceuticals Inc., USA recalls Clobetasol Propionate Foam, 0.05%, a) 50 g pack (NDC 68462-608-27) and b) 100 g pack (NDC 68462-608-94), Rx only,
Glenmark Pharmaceuticals recalls 0.05% Clobetasol Propionate Foam due to defective delivery system causing it to not foam or leak liquid. Rx only products with specific NDCs and expiration dates are affected.
GlenmarkNov 15, 2019 - Lower riskDrug
Grato Holdings, Inc. recalls Colostat, Homeopathic Remedy, 1 fl. oz. (30 mL) per bottle, 20% Ethanol, Dist. by Energique, Inc., 201 Apple Blvd.,
Grato Holdings recalls Colostat homeopathic remedy due to incorrect labeling. This may cause confusion about intended use. Consumers should check product details and contact the manufacturer for clarification.
Grato HoldingsNov 15, 2019 - Lower riskDrug
Akorn, Inc. recalls MYORISAN (isotretinoin capsules, USP), 20mg, packaged in 30-count Capsules (3 x 10 Prescription Packs) per box, Rx
Akorn recalls Myorisan 20mg capsules (NDC 61748-302-13) after customer reports a carton contained one 40mg blister pack mistakenly with two 20mg packs. This could lead to incorrect dosing.
AkornNov 15, 2019 - Lower riskDrug
Rising Pharmaceuticals, Inc. recalls Timolol Maleate USP, 0.5%, 5 mL, Sterile Opthalmic Solution, Rx Only, For Topical Application in the Eye, Distributed
Rising Pharmaceuticals recalls Timolol Maleate 0.5% eye drops due to label mix-up with 0.25% solution. This could lead to incorrect dosing if used without proper labeling.
Rising PharmaceuticalsNov 15, 2019 - Lower riskFood
SARA LEE FROZEN FOODS recalls Chef Pierre 37 Ounce Pumpkin Spice Latte Pie, in foil pie pan with dome lid, frozen, 4 pies per wholesale case, with
Sara Lee recalls 4-packs of frozen Pumpkin Spice Latte Pie with undeclared FD&C Red 40 dye. Consumers should check lot codes and contact for details.
Sara LeeNov 15, 2019 - Stop using nowFood
Kraft Foods Global Inc recalls CHEESE NIPS (11 oz. BOX), Retail UPC - 0 44000 03453 5, Best When Used By Date - 18MAY20, 19MAY20, 20MAY20
Kraft Foods recalls 11oz Cheese Nips boxes with UPC 044000034535 from May 18-20, 2020 due to small yellow plastic pieces. Consumers should stop using affected products.
KraftNov 15, 2019 - Lower riskFood
THE KRAFT HEINZ COMPANY recalls Breakstones 4% Milkfat Small Curd Cottage Cheese, in 24 oz. Plastic Tub, with UPC 0 21000 12284 4, 12 packages per case
Kraft Heinz recalls 24oz cottage cheese tubs with UPC 021000122844 due to potential red plastic and metal pieces from production. Consumers should check packaging and contact for details.
Kraft HeinzNov 15, 2019 - Use cautionVehicle
DODGE DURANGO (2013) recall — Electrical System
Chrysler recalls 2013 Dodge Durangos with electrical issues that may cause sudden stalling, increasing crash risk. Owners must replace fuel pump relay and wire harness to prevent vehicle stalls.
ChryslerNov 14, 2019 - Use cautionVehicle
RAM 1500 (2019) recall — Steering
Chrysler recalls 2019 RAM 1500 trucks with potential power steering loss causing inconsistent steering, especially at low speeds. Owners must have EPS gear assembly replaced free by dealers.
ChryslerNov 14, 2019 - Use cautionVehicle
CHEVROLET SILVERADO 2500 (2020) recall — Seat Belts
GM recalls 2020 Chevrolet Silverado 2500s with carpet floor covering due to fire risk from seat belt pretensioner bracket openings. Owners must have dealers close the opening free of charge.
ChevroletNov 14, 2019 - Lower riskMedical device
Medtronic Perfusion Systems recalls Medtronic Affinity, 38um Arterial Filter, Catalog number REF 351
Medtronic recalls Affinity 38um Arterial Filters with excess plastic (flash) that could cause blockages. Affected units have specific catalog and lot numbers.
Medtronic Perfusion SystemsNov 14, 2019 - Lower riskMedical device
Hardy Diagnostics recalls HardyCHROM MRSA,REF; G307, LOT: 447694, A selective and differential chromogenic medium for the qualitative direct
Hardy Diagnostics recalls HardyCHROM MRSA G307 lot 447694 due to false positive results from MSSA breakthrough. This medium may misidentify MRSA in nasal tests.
Hardy DiagnosticsNov 14, 2019 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis zee/ zeego Interventional Fluoroscopic X-Ray System, Model Number: 10094142, Software Version: VC21C
Siemens recalls Artis zee floor Interventional Fluoroscopic X-Ray Systems with model 10094142 and software VC21C due to collision sensor causing tabletop movement delays during procedures.
SiemensNov 14, 2019 - Lower riskMedical device
Cardinal Health Inc. recalls Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent System devices are designed to deliver a
Cardinal Health recalls PRECISE Nitinol Stent Systems with incorrect MRI labeling. The devices are labeled "MRI Safe" instead of "MRI Conditional". This could cause issues with MRI scans. Consumers should check their product codes.
Cardinal HealthNov 14, 2019 - Use cautionMedical device
Abbott Diabetes Care, Inc. recalls Precision Xtra Blood Glucose & Ketone Monitoring System, UDI: 00093815715023, 00093815988144
Abbott recalls Precision Xtra meters due to uncleared disinfection instructions that may cause infection. Check your device UDI and follow safety guidelines.
AbbottNov 14, 2019 - UnratedDrug
Wisconsin Pharmacal Company, LLC recalls Yeast Arrest, Homeopathic Formula, Vaginal Support suppositories, packaged in a) 14-count carton (NDC 68093-0730-1 and
Wisconsin Pharmacal recalls Yeast Arrest vaginal suppositories due to cGMP violations. Products sold in 14-count and 28-count cartons with specific lot numbers. No remedy provided in official notice.
Wisconsin PharmacalNov 14, 2019 - UnratedDrug
AVKARE Inc. recalls AVKARE Ranitidine Tablets, USP 150 mg Rx Only Manufactured for: AvKARE, Inc. Pulaski, TN 38478 Manufactured by: Amneal
AVKARE recalls 1000, 180, and 60-count ranitidine tablets with impurity N-nitrosodimethylamine (NDMA) that may pose health risks. Consumers should check NDC numbers and expiration dates.
AVKARENov 14, 2019 - Stop using nowConsumer product
Quest Products Recalls ALOCANE Emergency Burn Pads Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning
Quest Products recalls ALOCANE Emergency Burn Pads due to non-child-resistant packaging. Young children could poison themselves by putting the pads in their mouths. Return for free child-safe gel or refund.
Quest ProductsNov 14, 2019 - Stop using nowConsumer product
Kenmore Microwave Ovens Recalled Due to Burn Hazard; Made by Guangdong Galanz; Sold Exclusively at Sears and Sears Hometown and Outlet Stores
1,000-watt Kenmore Elite microwaves made in April 2017 with serial numbers starting 170427 have incorrect wiring that can cause exterior temperatures over 183°F, posing burn risk. Consumers must stop using and contact Sears for repair.
KenmoreNov 14, 2019 - Stop using nowConsumer product
Briggs & Stratton Recalls Snapper Rear Engine Riding Mowers Due to Injury Hazard
Briggs & Stratton recalls Snapper rear-engine mowers with a faulty blade engagement lever that can keep the blade engaged after releasing the disengagement pedal, causing injury. Consumers must stop using and get a free repair.
Briggs & StrattonNov 14, 2019 - Use cautionMeat & poultry
Creative Food Processing Recalls Poultry Products Due to Misbranding and Undeclared Allergens
USDA recalls 1,941 lbs of raw chicken products with undeclared wheat allergen. Consumers urged to discard items purchased between April 2019 and November 2019.
Creative Food ProcessingNov 13, 2019
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.