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- Lower riskDrug
Sun Pharmaceutical Industries, Inc. recalls Sumatriptan Succinate Tablets, 100 mg packaged in 9 (1X9) Unit-of-use blister card, (62756-0522-69), Rx only, Sun
Sun Pharmaceutical recalls 100mg Sumatriptan tablets due to impurities. These prescription migraine meds may have harmful substances that could cause health issues. Check your blister packs for the specific lot numbers listed.
SunDec 26, 2019 - Lower riskFood
Bay State Milling Co. recalls SimplySafe Sesame Seed Hulled; 49lbs bag; Lot #PBAT10025110
Bay State Milling Co. recalls SimplySafe Sesame Seed Hulled (49lb bags, Lot #PBAT10025110) due to possible Salmonella contamination. Consumers should check product labels for the lot number and take appropriate action if affected.
Bay State Milling Co.Dec 26, 2019 - Stop using nowFood
Veggie Noodle Co recalls Cece's Veggie Co. brand Fresh Veggie Ramen with Chicken Broth (11.5 oz, UPC 5228700653) packaged in a plastic tray
Veggie Noodle Co recalls Cece's Veggie Co. Fresh Veggie Ramen with Chicken Broth (11.5 oz) due to potential Listeria monocytogenes contamination. Consumers should avoid use.
Veggie Noodle CoDec 26, 2019 - Lower riskMedical device
Flowonix Medical Inc recalls Prometra II 20mL Pump. Catalog No. 13827 The device is an implantable infusion pump. GTIN-14 00810335020228
Flowonix Medical recalls Prometra II 20mL implantable infusion pumps with firmware version 0.26 manufactured from 2012 onward. The pump may not send error codes or emit alarms during valve system issues, potentially leading to undetected problems. Affected units have specific serial numbers listed in the recall.
Flowonix MedicalDec 24, 2019 - Lower riskFood
Sprouts Unlimited Inc recalls Clover sprouts packaged in 4 oz packages, Sprouts Unlimited, Inc. Marion, IA
Sprouts Unlimited recalls Clover sprouts from 2019 with E. coli O103 outbreak linked to Iowa illnesses. Consumers should avoid these products.
Sprouts UnlimitedDec 24, 2019 - UnratedFood
The H.T. Hackney Co. LLC recalls Fresh Location Protein Snack Tray 6.44oz, UPC: 8-5511000804-6
Fresh Location Protein Snack Tray 6.44oz (UPC 8-5511000804-6) recalled due to potential Listeria monocytogenes contamination. Consumers should check best-by dates and contact the company for details.
Fresh LocationDec 24, 2019 - Lower riskFood
Dierbergs Markets, Inc Corporate Office recalls Dierbergs Kitchen Remoulade packaged in 12 OZ containers, UPC 2393330149 and 24616200000
Dierbergs recalls 12oz remoulade containers with UPCs 2393330149 and 24616200000 due to potential Listeria monocytogenes contamination in hardboiled eggs used for salad and deli products.
DierbergsDec 24, 2019 - Use cautionVehicle
DYNAMAX REV (2018) recall — Engine And Engine Cooling
Forest River recalls 2016-2018 Dynamax Rev motorhomes with overheated fan motors that could cause fire. Owners must contact customer service for free replacement of the engine cooling fan module.
Forest RiverDec 23, 2019 - Use cautionVehicle
RIVERSIDE INTREPID (2020) recall — Equipment
Riverside is recalling 2020 Intrepid RVs with a stove flame inversion hazard that could cause fire. Owners must have a panel installed to shut off air flow between furnace and stove.
RiversideDec 23, 2019 - Lower riskMedical device
Philips North America, LLC recalls VesselNavigator application used with Philips Azurion (Azurion 7 Series) Software R1.2 and R2.0, and Philips Allura
Philips recalls Azurion 7 Series and Allura Xper R9 software versions R1.2 and R2.0 due to a defect causing digital subtraction angiography images to display without subtraction.
PhilipsDec 23, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00
Zimmer Biomet recalls Jamshidi Bone Marrow Aspiration Needles with potential expiration date mismatch between outer and inner labels. Affected lot numbers: 62754464, 62904: 63060634. Contact for remedy.
Zimmer BiometDec 23, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner
GE Healthcare recalls SIGNA Architect MRI systems that may record incorrect image dates due to installation workflow issues. Affected units need verification and correction to prevent inaccurate medical records.
GE HealthcareDec 23, 2019 - Lower riskMedical device
Carroll-Baccari, Inc. recalls LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP)
Carroll-Baccari recalls LemonPrep Tubes and Single-use cups due to Burkholderia cepacia contamination found in FDA samples. Consumers should check product labels for model numbers MD0019-T or MD0019-SUP.
Carroll-BaccariDec 23, 2019 - Lower riskMedical device
Nikon Metrology recalls Nikon Metrology XTH cabinet x-ray Systems which includes variations STH225, XTH225ST, and MCT225.
Nikon Metrology recalls XTH cabinet x-ray systems (STH225, XTH225ST, MCT225) due to potential x-ray emission failures from improper shielding attachment. No injuries reported; repair involves adding a bracket to secure shielding.
Nikon MetrologyDec 23, 2019 - Lower riskMedical device
Jjgc Industria E Comercio De Materials Dentarios Sa recalls Neodent Tapered Guided Surgery Drill, Article No. 103.436. UDI 07899878030041. The device is a dental burr.
Neodent recalls a dental burr with incorrect laser engraving that labels it as 4.3+ instead of 4.3 Tapered Guided Surgery Drill. This may cause confusion in dental procedures.
NeodentDec 23, 2019 - Lower riskDrug
GSK Consumer Health, Inc recalls Theraflu Cough Relief, Dextromethorphan HBr and Guaifensin, 6 packets per carton. Distributed by: GSK Consumer
GSK recalls Theraflu Cough Relief due to missing warning for sodium-restricted diets. Check labels for NDC codes and expiration dates to determine if your product is affected.
GSK Consumer HealthDec 23, 2019 - Use cautionFood
Sauer Brands, Inc. - New Century recalls Royal Farms Barbecue Dipping Sauce, Net Wt. 1.5 OZ Distributed by Royal Farms, Baltimore MD packaged in plastic cups,
Royal Farms recalls 1.5 oz barbecue dipping sauce due to undeclared soy. Check your plastic cups for lot code 19259SS.
Royal FarmsDec 23, 2019 - Stop using nowFood
Reichel Foods Inc. recalls Pro2Snax To The Max snack tray containing Sweet Gala Apples, Hard Boiled Egg, White Cheddar Cheese, and Dried
Reichel Foods recalls Pro2Snax To The Max snack trays with Listeria monocytogenes contamination. Consumers should avoid using these products to prevent potential foodborne illness.
Reichel FoodsDec 23, 2019 - Stop using nowFood
Great American Deli, LLC recalls Egg Salad Sandwich
Great American Deli recalls egg salad sandwiches with specific lot numbers due to potential Listeria monocytogenes contamination from a supplier. Consumers should check their lot numbers and contact the company for guidance.
Great American DeliDec 23, 2019 - Lower riskFood
Bakkavor Foods USA Inc. recalls TRADER JOE'S OLD FASHIONED Potato Salad NET WT. 20 OZ (1 LB 4 OZ) 567g DIST. & SOLD EXCLUSIVELY BY: TRADER JOE'S
Trader Joe's recalls potato salad potentially contaminated with Listeria monocytogenes. Consumers should check expiration dates and avoid using if expired.
Trader Joe'sDec 21, 2019 - Stop using nowMeat & poultry
Advance Pierre Foods Recalls Ready-to-Eat Ground Beef Products Due to Possible Foreign Matter Contamination
Advance Pierre Foods recalls ~15,739 lbs of RTE beef patties due to possible green soft plastic contamination. Discard or return immediately.
Advance Pierre FoodsDec 20, 2019 - Use cautionMeat & poultry
Ashland Sausage Co. Recalls Sausage Products Due to Possible Foreign Matter Contamination
Ashland Sausage Co. recalls pork sausages from Nov. 2019 with possible hard dark plastic contamination. Consumers are urged not to eat these products and should discard or return them.
Ashland Sausage Co.Dec 20, 2019 - Use cautionVehicle
PETERBILT 520 (2019) recall — Steering
PACCAR recalls 2018-2019 Peterbilt 520 trucks with improperly mounted steering bracket that may lock up steering, increasing crash risk. Owners must have bracket checked by dealer.
PeterbiltDec 20, 2019 - Use cautionVehicle
MERCEDES-BENZ GLC350E (2019) recall — Equipment
Mercedes-Benz recalls 2019 GLC350e models with foreign language airbag warnings that may prevent parents from knowing risks to children in front seats during crashes.
Mercedes-BenzDec 20, 2019 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls ADVIA Chemistry Lipase, Ref. No. 01984894 B01-4840-01, Siemens Material No. 10311896, UDI 00630414482446 - Product
Siemens Healthcare recalls ADVIA Chemistry Lipase products due to failed calibrations and imprecise patient sample results. Affected units may cause inaccurate pancreatic disease diagnoses.
Siemens HealthcareDec 20, 2019 - Lower riskMedical device
Custom Healthcare Systems, Inc. recalls Custom Healthcare Systems, Inc. Inpatient Dialysis Kit PAK-19244. Single use. Dialysis kit
Custom Healthcare Systems recalls inpatient dialysis kits PAK-19244 with latex in a component that wasn't labeled. This may cause allergic reactions. Contact for replacement.
Custom Healthcare SystemsDec 20, 2019 - Lower riskMedical device
Physio-Control, Inc. recalls LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an
Physio-Control
Physio-ControlDec 20, 2019 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Siemens ARTIS pheno, Model # 10849000. Interventional Fluoroscopic X-Ray System - Product Usage: Angiography system for
Siemens recalls ARTIS pheno model 10849000 interventional fluoroscopy systems due to risk of collision sensor blocking system movement. Affected units have specific serial numbers.
SiemensDec 20, 2019 - Lower riskMedical device
Arrow International Inc recalls Arrow StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1
Arrow recalls StimuCath Continuous Nerve Block Kit ASK-050:13F18A0547 due to incorrect expiration date on product lidstock. This may lead to improper use of the medical device.
ArrowDec 20, 2019 - Lower riskDrug
Island Kinetics, Inc. d.b.a. CoValence Laboratories recalls PCA Skin Blemish Control Bar, 3.2 oz/90g, Salicylic acid 2% - Acne cleanser, For external use only, Distributed by PCA
CoValence Laboratories recalls PCA Skin Blemish Control Bar (3.2 oz) due to excessive salicylic acid content. This may cause skin irritation or other adverse effects. Consumers should check product details and contact the company for guidance.
CoValence LaboratoriesDec 20, 2019
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