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- Stop using nowMedical device
Nova Ortho-Med Inc recalls Star 8 Rolling Walker/Rollator, Items: 4258/ BK(Black)/ BL(Blue)/ DB(Sky Blue)/ PL(Purple)/ RD(Red)
Nova Ortho-Med recalls Star 8 rolling walkers due to front fork detachment risk. Check serial numbers and purchase date for details.
Nova Ortho-MedOct 7, 2019 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Software versions syngo CT VB20 running on the following Siemens SOMATOM CT Scanner. SOMATOM Force (Model #10742326),
Siemens recalls specific SOMATOM CT scanners with syngo CT VB20 software due to scan aborts and system crashes. Affected models include SOMATOM Force, Definition As, and others. Contact Siemens for remedy.
SiemensOct 7, 2019 - Lower riskMedical device
Implant Direct Sybron Manufacturing LLC recalls Legacy 3 Implant, Size: 4.2mmD x 13mmL, 3.5mmD Platform, REF: 864213
Sybron recalls Legacy 3 dental implants with incorrect sizes that could require surgery rescheduling. Affected units include specific dimensions and lot numbers.
SybronOct 7, 2019 - Lower riskMedical device
Beckman Coulter, Inc. recalls UniCel DxH Slidemaker Stainer (DxH SMS) and UniCel DxH Slidemaker Stainer II (DxH SMS II) - Product Usage: The intended
Beckman Coulter recalls UniCel DxH Slidemaker Stainer (DxH SMS) and UniCel DxH Slidemaker Stainer II (DxH SMS II) due to potential cell carryover causing erroneous lab results. Affected units have specific serial numbers and catalog numbers.
Beckman CoulterOct 7, 2019 - Lower riskMedical device
Baylis Medical Company Inc. recalls TorFlex Transseptal Guiding Sheath ; Model numbers: TF8-32-63-45, TF8-32-63-55, TF8-32-63-90, TF8-32-63-135,
Baylis Medical recalls TorFlex Transseptal Guiding Sheaths with specific model numbers due to potential packaging defects that could lead to infection if used in patients.
Baylis MedicalOct 7, 2019 - Lower riskDrug
Mylan Laboratories Limited (Sterile Products Division) recalls Rifampin for Injection, USP, 600 mg/vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103; NDC
Mylan recalls Rifampin injections for possible reduced effectiveness due to discoloration from impurities. Affected lots manufactured in 2019-2020.
MylanOct 7, 2019 - Lower riskFood
CTC Food International Inc recalls Orchids Dried Mushroom NET WT. 1 oz. (29G) Product of China UPC 0-74601-00947-2 Distributed by CTC Food International,
CTC Food International recalls Orchids Dried Mushroom (1 oz) due to undeclared sulfites. This may cause allergic reactions in sensitive individuals. Consumers should check UPC 0-74601-00947-2 and contact the company for details.
CTC Food InternationalOct 7, 2019 - Lower riskFood
Dole Packaged Foods, LLC recalls Dole Crushed Pineapple in 100% pineapple juice Manufactured For Dole Packaged Foods, LLC Westlake Village, CA 91361
Dole recalls crushed pineapple juice with potential plastic pieces. Consumers should check UPC 3890000613 and lot D18258 from The Philippines. No remedy specified.
DoleOct 7, 2019 - Use cautionVehicle
FORD ECONOLINE (2016) recall — Power Train
Ford is recalling certain 2016 Econoline vehicles with a risk of sudden power loss during transit, potentially increasing crash risk. Owners must contact Ford for free clutch replacement.
FordOct 6, 2019 - Use cautionVehicle
FORD EXPLORER (2017) recall — Suspension
Ford is recalling 2017 Explorer vehicles with potential rear suspension toe links that may fracture, causing sudden handling changes and crash risk. Owners can get free replacement parts at dealers.
FordOct 6, 2019 - Use cautionVehicle
AUDI E-TRON (2019) recall — Electrical System
Audi is recalling 2019 E-TRON models with a faulty seal that can let moisture into the high-voltage system, causing short circuits and fire risk. Owners must stop using the vehicle if warning lights appear with the message 'Electrical system: fault' and contact Audi Roadside Assistance.
AudiOct 6, 2019 - Use cautionVehicle
FOREST RIVER CHEROKEE (2019) recall — Equipment
Forest River is recalling 2018-2019 Cherokee travel trailers with incorrect federal placards that could lead to vehicle overload and instability. Owners should contact customer service for free replacement placards.
Forest RiverOct 5, 2019 - Use cautionVehicle
FOREST RIVER R-POD (2020) recall — Electrical System
Forest River is recalling 2019-2020 R-POD travel trailers due to a wiring issue that could cause fire if not fixed. Owners must have the wire moved from a 30A to 15A circuit.
Forest RiverOct 5, 2019 - Use cautionVehicle
MERCEDES-BENZ METRIS (2017) recall — Steering
Mercedes-Benz Metris 2017 vehicles with corroded power steering bolts may lose steering assist, increasing crash risk. Owners must have bolts replaced by dealers.
Mercedes-BenzOct 4, 2019 - Use cautionVehicle
CHEVROLET G4500 (2018) recall — Exterior Lighting
North Central is recalling certain 2016-2018 Chevrolet G4500 ambulances with Whelen brake lights that may illuminate without pressing the brake pedal, risking crashes.
North CentralOct 4, 2019 - Use cautionVehicle
FIAT 500X (2019) recall — Air Bags
Chrysler recalls certain 2019 Fiat 500X vehicles with software that may disable airbag safety features. Owners must contact dealers for free software updates to prevent injury risks in crashes.
ChryslerOct 4, 2019 - Use cautionVehicle
BMW X4 (2019) recall — Air Bags
BMW is recalling certain 2019 X4 models due to potential passenger air bag deployment issues. Owners may need to have the instrument panel assembly replaced to prevent injury risk in crashes.
BMWOct 4, 2019 - Use cautionMedical device
Cordis Corporation recalls Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Cordis recalls MAXI LD PTA Dilatation Catheters made with expired inner body. This could cause device failure during cardiovascular procedures. Affected units have specific catalog and lot numbers.
CordisOct 4, 2019 - Lower riskMedical device
Neocis Inc. recalls Neocis Guidance System Fiducial Array - Product Usage: The Neocis Guidance System (NGS) is a computerized navigational
Neocis recalls Fiducial Array units with serial numbers FA-0128-02, FA-0129-02, FA0130-02 due to potential failed landmark checks during dental implant surgery. Affected users should contact Neocis for guidance.
NeocisOct 4, 2019 - Lower riskMedical device
Roche Diagnostics Operations, Inc. recalls Roche Homocysteine-In vitro test for the quantitative determination of total L-homocysteine in human serum and plasma
Roche recalls homocysteine test kits for cobas c701/702 systems due to calibration failures. Affected lots may give inaccurate results. Contact Roche for details.
RocheOct 4, 2019 - Use cautionMedical device
Ventana Medical Systems Inc recalls Model Number: 06917259001 UDI: 04015630976010 - Product Usage: The System s intended use environment includes anatomic
Ventana Medical Systems recalls HE 600 histology instruments with model 06917259001 due to cleaning solution leaking into electrical wiring, risking burned components in lab settings.
VentanaOct 4, 2019 - Use cautionMedical device
Teleflex Medical recalls WECK Hem-O-Lok AutoEndo5, 5mm Automatic Endoscopie Hem-o-lok Applier, REF 543965 Automatic Endoscopic Surgical Ligating
Teleflex Medical recalls WECK Hem-O-Lok AutoEndo5 5mm clip appliers due to misloading/jamming risks that could cause clips to fall out or break.
Teleflex MedicalOct 4, 2019 - Stop using nowMedical device
ICU Medical, Inc. recalls REF: Z2812, 121" 10 Drop Primary Set w/5 MicroClave, Remv 2 Gang 4-Way Stopcocks, Rotating Luer, 2 Ext, Sterile R, UDI:
ICU Medical recalls 10-drop IV sets with potential 15-drop cannula causing under-delivery of critical medication. Affected units include specific lot numbers and model REF: Z2812. Stop using immediately to prevent serious health risks.
ICU MedicalOct 4, 2019 - Lower riskMedical device
Randox Laboratories, Limited recalls Randox Liquid Cardiac Controls Catalogue Numbers CQ5053.
Randox recalls Liquid Cardiac Controls with catalogue number CQ5053 due to reduced N-TproBNP recovery in recent batches. Affected units may have inaccurate cardiac test results.
RandoxOct 4, 2019 - Use cautionMedical device
Baxter Healthcare Corporation recalls Prismaflex Control Unit, software versions below 7.21
Baxter recalls Prisma: Control units with software versions below 7.21 due to communication errors that could interrupt therapy or cause blood loss. Affected units have specific product codes and lot numbers.
Baxter HealthcareOct 4, 2019 - Use cautionDrug
KVK-Tech, Inc. recalls Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK
KVK-Tech recalls 384 bottles of Methylphenidate Hydrochloride Oral Solution due to fiber particles. Check your batch and expiration date.
KVK-TechOct 4, 2019 - Lower riskFood
Gullah Gourmet, Inc. recalls Nana's Been a Nut Bread NET WT. 11oz/311.74g cloth bag CONTAINS WHEAT AND SOY. MADE ON EQUIPMENT THAT MAKES PRODUCTS
Gullah Gourmet recalls Nana's Been a Nut Bread due to missing walnut ingredient statement. The product was made on equipment that also handles tree nuts, posing a risk for people with nut allergies.
Gullah GourmetOct 4, 2019 - Use cautionConsumer product
Harbor Freight Tools Recalls Gordon Folding Knives Due to Laceration Hazard
Harbor Freight Tools recalls Gordon folding knives due to laceration risk from locking mechanism failure. Affected knives may cause cuts during use. Return for $5 gift card refund.
Harbor Freight ToolsOct 4, 2019 - Stop using nowConsumer product
fluidfreeride Recalls Mercane WideWheel Electric Scooters Due to Fall and Injury Hazards (Recall Alert)
Fluidfreeride recalls Mercane WideWheel electric kick scooters due to brake caliper failure risks causing falls and serious injuries. Affected models have gray aluminum alloy frames with four-inch wheels.
fluidfreerideOct 4, 2019 - Use cautionConsumer product
Fit For Life Recalls SPRI Ultra Heavy Resistance Bands Due to Injury Hazard
Fit For Life recalls SPRI Ultra Heavy Resistance Bands due to risk of injury from bands separating from handles. Affected units have specific model numbers and packaging details.
Fit For LifeOct 4, 2019
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