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
34,894 found- UnratedDrug
G & W Laboratories, Inc. recalls Ciclopirox Olamine Cream USP, 0.77%, packaged in a) 15 g tubes (NDC 0713-0638-15); b) 30 g tubes (NDC 0713-0638-31);
G & W Laboratories recalls specific lots of Ciclopirox Olamine Cream USP, 0.77% due to intermittent yellow discoloration. Check your tube's lot number and expiration date.
G & W LaboratoriesJan 19, 2018 - UnratedDrug
Flawless Beauty LLC recalls Ling Zhi capsules
Flawless Beauty LLC recalls all Ling Zhi capsules sold individually or in kits due to being marketed without FDA approval. This unapproved drug poses health risks and requires immediate attention.
Flawless BeautyJan 19, 2018 - Stop using nowFood
National Frozen Foods Corporation--Seattle recalls IQF Green beans, sold as Not Ready To Eat (NRTE) product for use in foodservice or manufacturing applications. The
National Frozen Foods Corporation recalls IQF green beans for foodservice use due to potential Listeria monocytogenes contamination. Consumers should not use these products as they pose a risk of serious illness.
National Frozen Foods CorporationJan 19, 2018 - Use cautionFood
Wegmans Food Markets, Inc. recalls Wegmans Ready To Cook Lobster & Shrimp Steam Pot, Sold by the lb. UPC: 2-16326-00000
Wegmans recalls Ready To Cook Lobster & Shrimp Steam Pots due to undeclared soy lecithin. Check your UPC and dates for details.
WegmansJan 19, 2018 - Lower riskFood
Wienke LLC recalls Wienke's Market Strawberry Raspberry Jam, Net Wt. 8 oz (226g), UPC 14106-00235. Refrigerate after opening. Ingredients:
Wienke recalls strawberry raspberry jam produced before January 17, 2018 due to butter not being declared on labels. Consumers should check UPC 14106-00235 and refrigerate after opening.
WienkeJan 19, 2018 - Stop using nowConsumer product
Panasonic Recalls Flat Screen Televisions and Swivel Stands Due to Tip-Over Hazard
Panasonic recalls 55-inch LED televisions with swivel stands due to risk of tipping over, potentially causing injury or death to children. Consumers must detach the stand and contact Panasonic for a repair kit.
PanasonicJan 19, 2018 - Use cautionMeat & poultry
Café Spice GCT Inc., Recalls Ready-To-Eat Chicken Salad Products Due to Misbranding and an Undeclared Allergen
Café Spice recalls ready-to-eat chicken salad products due to misbranding and an undeclared milk allergen. Consumers are urged not to consume these products.
Café SpiceJan 18, 2018 - Lower riskMeat & poultry
Duke Sandwich Productions, Inc. Recalls Ready-To-Eat Chicken Salad Products Due to Misbranding
Duke Sandwich Productions recalls chicken salad products from Dec. 2017 with misbranding issues. Products were packaged with two different names and may be sold in Alabama, Georgia, North Carolina, South Carolina, Tennessee, and Virginia.
Duke SandwichJan 18, 2018 - Lower riskMedical device
Neuropro Spinal Jaxx recalls Spinal Jaxx Interbody Fusion Device, Model: 100001-511, Size: 9 H x 10 W x 25 L Product Usage: The Spinal Jaxx
Neuropro Spinal Jaxx recalls Spinal Jaxx Interbody Fusion Device Model 100001-511 due to incorrect implant size etching. The box size is correct but the implant itself has a wrong size marking.
Neuropro Spinal JaxxJan 18, 2018 - Lower riskMedical device
Beckman Coulter Inc. recalls AutoMate 2550 "High Speed" Catalog Number ODL25255; AutoMate 1250 "Standard" Catalog Number ODL25125. Chemistry
Beckman Coulter recalls AutoMate 2550 and 1250 chemistry analyzers due to pipette tip sensor misalignment causing cross-contamination of patient samples.
Beckman CoulterJan 18, 2018 - Lower riskMedical device
Angiodynamics Inc. (Navilyst Medical Inc.) recalls Fluid Management Convenience Kits (Angioplasty Kits) intended to be used in Fluid Management and/or Invasive Pressure
Angiodynamics recalls fluid management kits with specific lot numbers due to assembly issues causing minor procedure delays. Affected kits may not function properly during medical procedures.
AngiodynamicsJan 18, 2018 - Use cautionConsumer product
Hillsdale Furniture Recalls Bar Stools Due to Fall Hazard (Recall Alert)
Hillsdale Furniture recalls Polston and Collin bar stools due to risk of seat loosening or breaking, causing falls. Consumers should stop using and get a refund.
Hillsdale FurnitureJan 18, 2018 - Use cautionConsumer product
Bed Bath & Beyond Recalls Hudson Comforters by UGG Due to Risk of Mold Exposure
Bed Bath & Beyond recalls Hudson comforters by UGG due to mold exposure risk. Affected items sold in garnet, navy, gray, and oatmeal colors. Return for full refund to avoid respiratory issues in vulnerable users.
UGGJan 18, 2018 - Stop using nowConsumer product
Bassinets Recalled Due to Violation of Bassinet & Cradle Standard; Made By Multipro (Recall Alert)
Multipro Baby Cradle N Swings recalled due to fall and entrapment risks. Stop using immediately and dispose of product.
MultiproJan 18, 2018 - Use cautionMedical device
Spacelabs Healthcare Inc recalls Spacelabs Healthcare Xhibit Telemetry Receiver, Model 96280, software version 1.1, physiological patient monitor (with
Spacelabs Healthcare recalls Model 96280 telemetry receivers with software version 1.1 due to telemetry beds dropping off the central station, causing loss of patient monitoring.
Spacelabs HealthcareJan 17, 2018 - UnratedMedical device
Olympus Corporation of the Americas recalls Uretero-reno fiberscope URF-P6RP6
Olympus recalls URF-P6RP6 ureterorenal fiberscopes due to potential breakage during surgery, which could cause injury. All units with serial numbers are affected.
OlympusJan 17, 2018 - UnratedMedical device
Olympus Corporation of the Americas recalls Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
Olympus recalls URF-V2 and URF-V2R uretero-reno videoscopes due to potential breakage during surgery. All units are affected. No remedy specified in recall notice.
OlympusJan 17, 2018 - Stop using nowDrug
Magno Humphries Laboratories, Inc recalls Senna Laxative (sennosides) tablets, 8.6 mg, 100-count bottles, Manufactured for: Basic Drugs, Inc., Vandalia, Ohio
Magno Humphries recalls Senna Laxative bottles due to a label mix-up. Bottles labeled as Senna may contain Naproxen Sodium tablets.
Magno Humphries LaboratoriesJan 17, 2018 - Lower riskFood
Palmer and Company recalls Sea Salt Caramel Hearts, Net Wt 12 OZ (340 g), Made by Palmer Candy Company, Sioux City, Iowa. UPC 77232-17091
Palmer and Company recalls Sea Salt Caramel Hearts (12 oz) due to undetected peanuts. This poses a risk for people with peanut allergies. Consumers should check the UPC 77232-17091 label for affected items.
Palmer and CompanyJan 17, 2018 - Lower riskFood
Empresas Barsan, Inc. recalls TITAN, 24 rellenos de papas, (potato puffs), Net WT 6.75 LB (pounds)
Empresas Barsan recalls 24-pack TITAN potato puffs due to missing sodium bisulfite ingredient label on product packaging. Consumers should check for expiration dates on yellow labels.
Empresas BarsanJan 17, 2018 - Lower riskFood
CHOBANI recalls Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogurt with Graham Crackers & White Chocolate, 4-packs, 4/5.3 oz
Chobani recalls 4-packs of Flip Key Lime Crumble yogurt due to incorrect 'No Gluten' label despite wheat ingredients. Consumers should check for wheat in ingredients and contact Chobani for details.
ChobaniJan 17, 2018 - Use cautionVehicle
INDIAN ROADMASTER (2017) recall — Electrical System
Indian recalls 2015-2017 Roadmaster motorcycles with brake light that stays on when brakes aren't applied, causing potential crashes. Owners must get free wiring harness fix.
IndianJan 16, 2018 - Use cautionVehicle
FORD EXPEDITION (2018) recall — Visibility
Ford is recalling 2018 Expedition vehicles with second row window control modules that may stop moving, increasing injury risk if a finger is pinched. Owners must have windows inspected and replaced if needed.
FordJan 16, 2018 - UnratedMedical device
Medtronic Perfusion Systems recalls Medtronic AFFINITY NT, Cardiotomy/Venous Reservoir (CVR) with Filter, 540 The AFFINITY(R) NT Cardiotomy/Venous
Medtronic recalls AFFINITY NT Cardiotomy/Venous Reservoirs with Filter due to possible sterile barrier breach in the pouch. This could lead to infection during surgery. Affected units include all lots of the 540 model.
MedtronicJan 16, 2018 - UnratedDrug
Sun Pharmaceutical Industries, Inc. recalls DOXOrubicin Hydrochloride Liposome Injection, 20 mg/10 ml (2 mg/mL), 10 mL Single Use Vial, Distributed by: Sun
Sun Pharmaceutical recalls DOXOrubicin Hydrochloride Liposome Injection vials due to lack of sterility assurance. This could lead to infections if the product is not properly sterilized during manufacturing.
Sun PharmaceuticalJan 16, 2018 - UnratedDrug
Fresenius Kabi USA, LLC recalls Vecuronium bromide for Injection, 10 mg vials, Rx only, Mfd. for: Fresenius Kabi, Lake Zurich, IL 60047, Made in India,
Fresenius Kabi recalls 10mg Vecuronium bromide vials (NDC 63323-781-10, Lot ZG603) due to impurities detected in stability testing. This medication is for injection only and requires immediate action.
Fresenius KabiJan 16, 2018 - Use cautionFood
Ottogi America Inc recalls Ottogi Rice Cake Soup, 6.4oz. UPC 6 45175 89093 52; Item Number 29409101; Ingredients: 1. Rice Cake: Rice Water, Salt,
Ottogi America Inc recalls 6.4oz Rice Cake Soup due to undeclared milk (sodium caseinate). Check your UPC and expiration date.
OttogiJan 16, 2018 - Lower riskFood
Frog Holler Ltd. recalls Cherry Tomatoes, packaged in a pint sized plastic clamshell, no labeling
Frog Holler Ltd. recalls cherry tomatoes in pint plastic clamshells without labeling due to potential Salmonella contamination. Products distributed from Jan 2018 may be unsafe.
Frog HollerJan 16, 2018 - Stop using nowConsumer product
Fujifilm Recalls Power Adapter Wall Plugs Sold with Digital Cameras Due to Shock Hazard
Fujifilm recalls AC-5VF power adapter wall plugs with digital cameras XP90, XP95, XP120, XP125, X-A3 and X-A10 due to risk of cracking and shock hazards. Stop using immediately and get a free replacement.
FujifilmJan 16, 2018 - Lower riskMedical device
Smith & Nephew, Inc. recalls LEGION(TM) HEMI STEP TIBIAL WEDGE RK/HK, 5 MM, SIZE 3-4 LT.MDL/RT-LAT, REF 71423432 Product Usage: The constrained knee
Smith & Nephew recalls Legion Hemi Step Tibial Wedge RK/HK implants due to incorrect screw packaging. This affects constrained knee surgery patients. Contact for replacement.
Smith & NephewJan 15, 2018
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