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
34,956 found- Stop using nowMeat & poultry
Johnston County Hams Recalls Ready-To-Eat Ham Products Due to Possible Listeria Contamination
Johnston County Hams recalls ~89,096 lbs of ready-to-eat hams due to possible Listeria monocytogenes contamination. Check your fridge and discard immediately.
Johnston County HamsOct 3, 2018 - Use cautionMedical device
Medtronic Inc. recalls Medtronic MiniMed 630G 6025805-003_C, Rx Only Medtronic MiniMed 670G 6025805-005_B, Rx Only Medtronic MiniMed 640G
Medtronic recalls insulin pumps with version 4.10 software that may fail to make audio alerts for system notifications or glucose alerts, potentially causing users to miss critical warnings.
MedtronicOct 3, 2018 - Use cautionMedical device
GE Medical Systems, LLC recalls SIGNA Architect system Product Usage: The Signa Architect system is a whole body magnetic resonance scanner designed to
GE Medical Systems recalls Signa Architect MRI systems with specific serial numbers due to potential serious burns if patient touches warm bore surface without proper padding. Affected units may need safety adjustments.
GE Medical SystemsOct 3, 2018 - Stop using nowDrug
Pfizer Inc. recalls Magnesium Sulfate in Water for Injection (0.325 mEq Mg++/mL) 40 mg/mL, 20 g Total, 500 mL Single-Dose Container bag, Rx
Pfizer recalls 94,752 bags of Magnesium Sulfate in Water for Injection due to a mispack hazard involving Heparin. Check your lot numbers.
PfizerOct 3, 2018 - Lower riskDrug
InvaGen Pharmaceuticals, Inc. recalls Amlodipine Besylate USP 10 mg Tablets, 1000-count bottles, Rx Only, Manufactured by: Cipla Ltd., Verna Goa, India,
InvaGen Pharmaceuticals recalls 10 mg Amlodipine Besylate tablets due to subpotent drug quality. This means the medication may not be as effective as labeled, potentially requiring higher doses for treatment.
InvaGen PharmaceuticalsOct 3, 2018 - Lower riskDrug
Silver Star Brands recalls Native Remedies VaricoGo Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906.
Native Remedies VaricoGo Oral Spray (2 fl oz) recalled due to microbial contamination. Consumers should contact Silver Star Brands for details.
Native RemediesOct 3, 2018 - Lower riskFood
K.B. Pizza, Inc. recalls Son of Italy, Twin Pack Cheese Pizza Kit, 39 oz./2 pizzas per kit, Net Wt. 15.5 lbs. 6 pizza kits per case
K.B. Pizza Inc. recalls Son of Italy Twin Pack Cheese Pizza Kits that were left at room temperature for 24 hours, risking bacterial growth. Consumers should check use-by dates and contact the company for details.
Son of ItalyOct 3, 2018 - Stop using nowConsumer product
Yamaha Recalls Golf Cars, Personal Transportation and Specialty Vehicles Due to Crash Hazard (Recall Alert)
Yamaha recalls 2016-2018 golf cars and specialty vehicles due to accelerator pedal return spring that can break, causing crashes. Owners must stop using and contact dealers for free repairs.
YamahaOct 3, 2018 - Stop using nowConsumer product
Walmart Recalls Camp Axes Due to Injury Hazard
Walmart recalls Ozark Trail camp axes (model 60111140) due to risk of axe head detaching. Consumers should stop using and return for full refund.
Ozark TrailOct 3, 2018 - Lower riskMedical device
Straumann Manufacturing, Inc. recalls Neodent¿ GM Mini Conical Abutment - Product Usage: Mini Conical Abutments are intermediary prosthetic components to be
Straumann recalls Neodent GM Mini Conical Abutments due to laser engraved labels not matching the product in the package. This mismatch may cause incorrect installation. Affected units have specific model numbers and lot codes.
StraumannOct 2, 2018 - Lower riskMedical device
Randox Laboratories Ltd. recalls Liquid Cardiac Control, CQ5053
Randox recalls Liquid Cardiac Control CQ5053 due to unacceptable variation in Troponin T assay results. Affected units may cause inaccurate test results.
RandoxOct 2, 2018 - UnratedMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Medtronic CareLink Encore 29901 Programmer
Medtronic recalls CareLink Encore 29901 programmers due to potential cybersecurity risks allowing unauthorized software updates. All units are affected.
MedtronicOct 2, 2018 - Lower riskMedical device
Pfizer Inc. recalls Thermacare HeatWraps Menstrual a) UPC 0573302002 b) UPC 0573302044 Product Usage: Provides heat therapy for temporary
Pfizer recalls Thermacare HeatWraps Menstrual with UPCs 0573302002 and 0573302044 due to complaints of wraps coming apart and leaking granular material.
PfizerOct 2, 2018 - Use cautionMedical device
Arrow International Inc recalls AF w/AS 550 x 1-14ML/HR CPNB, Product code MVBXL- CPNB, Arrow AutoFuser Disposable Pain Control Pump
Arrow recalls disposable pain control pumps with possible cracks in fill port connectors that may cause leaks, leading to reduced pain relief and needing extra medication.
ArrowOct 2, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail 125 Deg 12x165mm, Item Number 816712165 The Affixus Hip Fracture Nail System, comprised of
Zimmer Biomet recalls Affixus Hip Fract: Set screw cannot advance or reverse, potentially causing improper fracture stabilization.
Zimmer BiometOct 2, 2018 - Lower riskDrug
Jubilant Cadista Pharmaceuticals, Inc. recalls Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg*, 90-count bottle, Rx only, Manufactured by: Jubilant Generics
Jubilant Cadista recalls 40mg Pantoprazole tablets with dark discoloration on edges. Stop using if you see brown spots. No remedy provided in official notice.
Jubilant CadistaOct 2, 2018 - Lower riskFood
CFS West Holdings Inc recalls Houlihan's Creamy Garlic Ranch Dressing potentially labeled as Horseradish Sauce, 1 gal containers Mfg. exclusively
Houlihan's Creamy Garlic Ranch Dressing may be mislabeled as horseradish sauce, hiding milk allergen. Consumers should check labels for potential allergic reactions.
Houlihan'sOct 2, 2018 - Lower riskFood
APOLLO FOOD INTERNATIONAL INC. recalls Mini Roll, The product comes in a 2.469 ounce pink plastic package marked with a production date of 2018.03.20 stamped
Apollo Food recalls Mini Roll snacks due to undeclared eggs. Products sold in pink 2.469 oz plastic packages with 2018.03.20 production date. Consumers should check for this specific packaging.
Apollo FoodOct 2, 2018 - Stop using nowConsumer product
AAA Innovations Recalls Promotional Cooler/Grills Due to Fire Hazard
AAA Innovations recalls promotional cooler/grills with wooden cabinets that can catch fire. Consumers should stop using and contact for $125 incentive or refund.
AAA InnovationsOct 2, 2018 - Stop using nowVehicle
NISSAN VERSA (2012) recall — Air Bags
Nissan is recalling certain 2012 Versa models due to passenger air bag inflator explosions that could cause serious injury or death. Owners must have the inflator replaced free of charge.
NissanOct 1, 2018 - Use cautionVehicle
KTM 1290 SUPER DUKE R (2018) recall — Service Brakes, Hydraulic
KTM recalls 2018 Super Duke R motorcycles with potential front brake master cylinder failure. Owners must contact KTM for free piston replacement.
KTMOct 1, 2018 - Use cautionMedical device
Mevion Medical Systems, Inc. recalls MEVION S250i
Mevion recalls S250i radiation therapy devices that may cause treatment interruptions if dDose1 interlock trips. Affected units have specific serial numbers and were sold in the U.S. Learn what to do.
MevionOct 1, 2018 - Lower riskMedical device
LeMaitre Vascular, Inc. recalls LeMaitre Vascular Pruitt F3¿-S Polyurethane Outlying Carotid Shunt, Sterile Model # 2014-10
LeMaitre Vascular recalls sterile polyurethane carotid shunt model 2014-10 (lot PFP1055) due to unsealed pouches risking infection. Affected units expire March 2020.
LeMaitre VascularOct 1, 2018 - Use cautionMedical device
Comet Technologies Usa Inc recalls YXLON Cougar Cabinet X-Ray System Product Usage: The products are generally used for non-destructive testing and
YXL:ON Cougar cabinet X-ray systems may fail to disconnect power when door opens, risking electrical hazards. Affected units were sold for non-destructive testing. Contact manufacturer for details.
YXLONOct 1, 2018 - Use cautionMedical device
Medical Components, Inc dba MedComp recalls C3 Wave App, v. 2.0.5
MedComp recalls C3 Wave App v. 2.0.5 due to ECG waves not appearing after iOS 12 update, risking incorrect PICC placement.
MedCompOct 1, 2018 - Use cautionMedical device
SVS LLC recalls PremierPro Aluminum Adjustable Walker
SVS LLC recalls PremierPro Model 7803 walkers due to FDA mandated stock recovery. Check lot CJH05041 and serial numbers J1805000577-J1805000864.
PremierProOct 1, 2018 - Lower riskFood
Pepsico Gatorade Plant recalls Gatorade Vanilla Protein Shake, 330-mL, Primary Package HDPE in a 12pk case
Pepsico Gatorade is recalling limited 12-packs of Vanilla Protein Shake due to potential Bacillus cereus bacteria contamination. Consumers should check for specific manufacture dates and use by dates.
Pepsico Gatorade PlantOct 1, 2018 - Lower riskFood
NUTRANEXT BUSINESS LLC recalls Internal Cleansing Kit Peppermint
NUTRANEXT recalls peppermint internal cleansing kits with elevated lead levels that may pose health risks. Consumers should check batch numbers and contact the company for details.
NUTRANEXTOct 1, 2018 - Use cautionConsumer product
UberScientific Recalls Topical Anesthetic Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning
UberScientific recalls topical anesthetic cream and spray due to non-child-resistant packaging. Risk of poisoning for young children if ingested or applied. Consumers should remove from reach and get free replacement or refund.
UberScientificOct 1, 2018 - Use cautionVehicle
KZRV SONIC (2018) recall — Equipment
KZRV is recalling 2017-2019 Sonic 190VRB travel trailers due to a risk of fire from a damaged LP manifold that can leak near the axle tube.
KZRVSep 28, 2018
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