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
FORD RANGER (2019) recall — Exterior Lighting
Ford recalls 2019 Ranger trucks with faulty rear light connectors that may cause tail lights to stop working, increasing crash risk. Owners should contact Ford for free repairs.
FordNov 21, 2019 - Use cautionVehicle
INTERNATIONAL HV (2020) recall — Service Brakes, Air
Navistar recalls 2020 International HV trucks with non-Quick Release Modulator Valves that may cause brake or tire fires. Owners must have the valve replaced free by dealers.
NavistarNov 21, 2019 - Use cautionVehicle
INTERNATIONAL HV (2020) recall — Engine
Navistar recalls 2019-2020 International HV vehicles with feature codes 12VXT/12VXU due to unintended vehicle movement when parking brake is engaged, increasing crash risk. Owners must update Engine Control Module free of charge.
NavistarNov 21, 2019 - Stop using nowVehicle
CADILLAC ESCALADE (2020) recall — Fuel System, Gasoline
GM recalls certain 2020 vehicles, including the Cadillac Escalade, due to a fuel pump missing a pressure regulator that can cause leaks and fire.
CadillacNov 21, 2019 - Lower riskMedical device
3M Company - Health Care Business recalls 3M Durapore Advanced, Surgical Tape, Model Numbers: 1590-0, 1590-1, 1590-2, 1590-3, 1591-0, 1591-1, 1591-2, 1591-3,
3M recalls Durapore Advanced Surgical Tape models 1590-0 to 1591-3 due to moisture exposure causing bond failure and potential fiber fraying. Affected items may not perform as intended or pose ingestion risk.
3MNov 21, 2019 - Lower riskMedical device
STANLEY BLACK & DECKER INC. recalls The products involved are DeWALT laser distance measurers, model numbers DW0165, DW0165S, DW0330S and Stanley Fatmax
Stanley Black & Decker recalls DeWALT and Stanley laser distance measurers with specific model numbers due to potential excessive laser radiation emissions exceeding Class II safety limits.
Stanley Black & DeckerNov 21, 2019 - Use cautionMedical device
Stryker GmbH recalls Stryker Pin To Rod Coupling External Fixation System Hoffmann II Compact - Pin To Rod Coupling 5/3-4mm Catalog #:
Stryker recalls a pin-to-rod coupling for fracture treatment. The device may not clamp pin and rod as intended, risking improper fixation. Affected units include specific model and lot numbers.
StrykerNov 21, 2019 - Use cautionMedical device
DeRoyal Industries Inc recalls DeRoyal KNEE BRACE, WARRIOR RECOVERY: 1) REF KB9000-01 2) REF 11-450A-00 3) REF 1150UTPP
DeRoyal recalls Warrior Recovery Knee Braces with specific lot numbers due to risk of hinge breaking. Consumers should check their product details to determine if affected.
DeRoyalNov 21, 2019 - UnratedMedical device
Caire, Inc. recalls CAIRE MODEL: FreeStyle Comfort Oxygen Concentrator - Product Usage: The FreeStyle Comfort Oxygen Concentrator is
Caire recalls four specific European model FreeStyle Comfort oxygen concentrators sold in the US that were not cleared for US use. These devices may not be safe for home use without proper medical clearance.
CaireNov 21, 2019 - Use cautionMedical device
Medtronic Inc. recalls Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and
Medtronic recalls specific MiniMed 630G System models with SmartGuard due to potential loose reservoir causing insulin delivery issues. Affected units may lead to hypoglycemia or hyperglycemia.
MedtronicNov 21, 2019 - Lower riskMedical device
Radiometer Medical ApS recalls ABL90 FLEX, model no. 393-090; and Spare Part Hemolyzer Units (902-980): R0526 - R0941 - Product Usage: are intended
Radiometer recalls ABL90 FLEX blood analyzers and spare hemolyzer units due to potential measurement errors in blood tests. Affected units may provide inaccurate results for certain blood measurements.
RadiometerNov 21, 2019 - Use cautionDrug
Preferred Pharmaceuticals, Inc recalls Ibuprofen Oral Suspension USP, 100 mg/5mL, 4 fl.oz. 118 mL, Rx only, Preferred Pharmaceuticals, Inc., Anaheim, CA. Mfg:
Preferred Pharmaceuticals recalls ibuprofen oral suspension with possible plastic particles. Consumers should check lot numbers and contact the company for details.
Preferred PharmaceuticalsNov 21, 2019 - Lower riskDrug
Pacira Pharmaceuticals, Inc. recalls EXPAREL, Bupivicaine Liposome Injectable Suspension, 1.3%, 266 mg/20 mL (13 mg/mL), Sterile, 20 mL vial, Rx only,
Pacira Pharmaceuticals recalls EXPAREL (bupivicaine) vials due to potential sub-potent drug levels. This affects certain 20mL vials manufactured in 2019. Contact for return instructions.
PaciraNov 21, 2019 - Lower riskFood
Frog Hollow Farm recalls Frog Hollow Holiday Fruitcake Incorrect ingredients: Organic butter, organic flour, organic sugar, organic eggs,
Frog Hollow Farm recalls Holiday Fruitcake from June 2019 with incorrect ingredients listed on labels. The product was sold with walnuts missing from the ingredient list.
Frog Hollow FarmNov 21, 2019 - Lower riskFood
Endorphin Farms, Inc. recalls Tobago Keys brand Coral Ridge Seafood Dipping Sauce 12 FL.OZ. (355 ml) and Peruvian Gold Grilling Sauce 12 FL.OZ (355
Endorphin Farms recalls Tobago Keys Coral Ridge Seafood Dipping Sauce and Peruvian Gold Grilling Sauce due to undeclared fish allergen in labels.
Endorphin FarmsNov 21, 2019 - Lower riskFood
Givaudan Flavours Corp recalls Nat Cashew Flavor Type, 11.34 kg in each 4.2 gallon blue HDPE jerri-can, UPC: 20355428593
Givaudan recalls 11.34 kg Nat Cashew Flavor Type in blue HDPE jerri-cans due to metal contamination in raw ingredients.
GivaudanNov 21, 2019 - Stop using nowConsumer product
SCARPA North America Recalls Ski Boots Due to Fall Hazard
SCARPA recalls Fall 2017 Maestrale RS and Men's Ski Boots due to shell cracking causing fall hazards. Consumers must stop using and return for free shell repair.
SCARPANov 21, 2019 - Use cautionConsumer product
RESURRECTIONbeauty Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
RESURRECTIONbeauty recalls Wintergreen Essential Oil due to non-child-resistant packaging, risking poisoning if young children swallow. Consumers should store out of reach and get free child-resistant caps.
RESURRECTIONbeautyNov 21, 2019 - Use cautionVehicle
CHEVROLET 5500HD (2019) recall — Wheels
Chevrolet 2019 5500HD vehicles with loose rear wheel lug nuts may cause wheel separation and crash risk. Owners must have rear lug nuts inspected and tightened by dealers free of charge.
ChevroletNov 20, 2019 - Lower riskMedical device
Datascope Corporation recalls Reinforced Introducer Sets Maquet 8 Fr., Part Number: 068400040310. It is an accessory to be used for percutaneous
Datascope Corporation recalls specific lots of Maquet Reinforced Introducer Sets due to potential for compromised sterility in breached pouches. Affected units may pose infection risks if used improperly.
MaquetNov 20, 2019 - Use cautionMedical device
Philips North America, LLC recalls ProxiDiagnost N90
Philips recalls ProxiDiagnost N90 medical imaging devices due to potential increased radiation exposure during scans. Affected units may require repair or replacement to ensure patient safety.
PhilipsNov 20, 2019 - Lower riskMedical device
B. Braun Medical, Inc. recalls Y-Type Blood Set, Catalog Number 490425
B. Braun recalls Y-Type Blood Set (Catalog 490425) due to potential leakage at blood filters and tubing joints. Affected units have specific lot numbers and expiration dates.
B. BraunNov 20, 2019 - Lower riskDrug
AuroMedics Pharma LLC recalls Mirtazapine Tablets, USP, 15 mg, 500-count tablets, Rx only, Distributed by: Aurobindo Pharma USA, Inc. Dayton, NJ
AuroMedics Pharma LLC recalls 500-count Mirtazapine 15mg tablets labeled as 7.5mg due to a labeling error. This could lead to incorrect dosing if used without proper medical guidance.
AuroMedicsNov 20, 2019 - Lower riskDrug
American Health Packaging recalls Ranitidine Tablets, USP, 150 mg, 100 Tablets (10 tablets x 10 blister card), Rx Only, Packaged and Distributed by:
American Health Packaging recalls 150mg Ranitidine Tablets due to potential N-Nitrosodimethylamine (NDMA) levels above FDA limits. Affected lots expired by December 2020.
American Health PackagingNov 20, 2019 - Lower riskDrug
Idelle Labs recalls SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant, Net Wt. 2.6 oz (73g) NDC# 41595-5509-2 UPC
Idelle Labs recalls SURE 48 hr Confidence Unscented invisible solid deodorant due to undeclared active ingredient. Consumers should check product labels and contact the company for details.
Idelle LabsNov 20, 2019 - Stop using nowFood
Lamb Weston Inc recalls Lamb Weston Grown In Idaho Crispy Hash Brown Dices, packaged in 28 ounce poly retail bags, 6 or 12 bags packaged in a
Lamb Weston recalls Grown In Idaho Crispy Hash Brown Dices because they may contain pieces of hard rubber. Check your lot numbers and UPCs.
Lamb WestonNov 20, 2019 - Lower riskFood
Kerry, Inc recalls DaVinci Gourmet, Classic Caramel Flavored Sauce, 128 FL OZ (1 GAL), in plastic jugs
Kerry recalls 128 fl oz caramel sauce due to undeclared milk allergen on back label. Consumers should check UPC 7-37384-06401-3 and lot number 0829950901 for affected products.
KerryNov 20, 2019 - Lower riskFood
WORLDWIDE SEAFOOD PRODUCTS LLC recalls 103200 - TIDAL SEAFOOD YELLOWFIN TUNA 10 lb, 2x10 lb cases and 103205 - TIDAL SEAFOOD YELLOWFIN TUNA 10 lb, 2x10 lb
Tidal Seafood is recalling yellowfin tuna products due to potentially elevated histamine levels. Consumers should check product codes and contact the company for details.
Tidal SeafoodNov 20, 2019 - Stop using nowConsumer product
Grace Digital Recalls EcoBoulder Speakers That Can Overcharge and Burst; Impact Hazard
ECOXGEAR recalls EcoBoulder Bluetooth speakers that can overcharge and burst, posing an impact hazard. Affected models include GDI-EXBM900 series with specific UPC codes. Consumers must stop using and get a free battery replacement kit.
ECOXGEARNov 20, 2019 - Stop using nowConsumer product
Deck Source Recalls Cutek Proclean Due to Violation of FHSA Labeling Requirements; Risk of Poisoning
Deck Source recalls Cutek Proclean Professional Wood Restoration due to missing 'poison' label on product, risking child poisoning. Consumers must stop using, move away from children, and get a free replacement label.
Deck SourceNov 20, 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.