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
35,025 found- Lower riskMedical device
Ortho Clinical Diagnostics Inc recalls VITROS Chemistry Products CKMB Slides: (1)VITROS CKMB Slides (60 Slide cartridge) Product Code:8058232 (2)VITROS CKMB
Ortho Clinical Diagnostics recalls VITROS CKMB Slides that may cause falsely elevated results due to CK-MM interference. Affected products include 60-slide and 18-slide cartridges with specific product codes and lot numbers.
Ortho Clinical DiagnosticsDec 11, 2020 - Lower riskMedical device
Qiagen Sciences LLC recalls therascreen PIK3CA RGQ PCR Kit (23) US IVD product- aid clinicians in identifying breast cancer patients who may be
Qiagen recalls PIK3:3CA RGQ PCR Kit (23) US IVD product due to potential false positive results for breast cancer mutation testing. Affected kits may misidentify patients for PIQRAY treatment.
QiagenDec 11, 2020 - Lower riskFood
Dreyers Grand Ice Cream, Inc. recalls Outshine Fruit & Cream Bars - Creamy Pineapple Coconut 6 fruit and dairy bars, 14.7 fl. oz. UPC: 41548 91817 4
Dreyers recalls 6-pack of Outshine Fruit & Cream Bars (Creamy Pineapple Coconut) due to foreign material complaints. Consumers should check UPC 41548 91817 4 and batch code 0230580204.
DreyersDec 11, 2020 - Lower riskFood
Netuno USA, Inc. recalls NETUNO Caribbean Red Snapper, Net Weight 10 Lbs (4.54 Kg), Item 101229, Product Must be Fully Cooked Prior to
Netuno USA recalls Caribbean Red Snapper (10 lbs) potentially contaminated with Salmonella. Product must be fully cooked before consumption. Learn if your item is affected and what to do.
NetunoDec 11, 2020 - Lower riskMedical device
Clerio Vision recalls Clerio Vision, extreme H2O monthly, MED, DIA 14.0 PWR -2.25, UPC 675506803334 (6 count) and UPC 675506804478 (12 count)
Clerio Vision recalls specific contact lens lots (UPC 675506803334 and 675506804478) due to incorrect lens power. These lenses may cause vision issues if used.
Clerio VisionDec 10, 2020 - UnratedMedical device
Accuray Incorporated recalls TomoTherapy Treatment Delivery System with iDMS - Product Usage: used as an integrated system for the planning and
Accuray recalls TomoTherapy Treatment Delivery System with iDMS due to potential dose rotation error during radiation therapy. Affected units have specific product codes and serial numbers. Contact Accuray for remedy details.
AccurayDec 10, 2020 - Use cautionMedical device
SenTec AG recalls SenTec Digital Monitor, Model SDM, is a portable stand-alone patient monitor indicated for continuous, noninvasive
SenTec recalls SDM patient monitors sold without isolation transformers for home use. These devices may not meet safety standards, risking electrical hazards. Affected units have specific serial numbers listed.
SenT:ecDec 10, 2020 - Lower riskMedical device
Remel Inc recalls Remel Blood Agar/MacConkey Agar Bi-Plate, REF: R02049
Remel recalls Blood Agar/MacConkey Agar Bi-Plates (Lot 150237) due to potential failure to grow patient isolates or QC organisms. Affected users should contact Remel for details.
RemelDec 10, 2020 - Use cautionMedical device
Argon Medical Devices, Inc recalls Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18C, 1/18 GA Flexcore Biopsy Needle, 1/7F
Argon Medical Devices recalls TLAB liver biopsy kits with potential sheath separation during use, risking surgical intervention. Affected kits have specific lot numbers.
Argon Medical DevicesDec 10, 2020 - Use cautionMedical device
GE Healthcare, LLC recalls GE Healthcare Precision 600FP, Classical R&F (radiographic and fluoroscopic) System - Product Usage: Intended for use
GE Healthcare recalls Precision 600FP radiographic systems due to potential monitor suspension detachment causing patient or operator injury.
GE HealthcareDec 10, 2020 - Use cautionMedical device
GE Healthcare, LLC recalls GE NM/CT 870 CZT system Model Number H3906CW - Product Usage: intended for general Nuclear Medicine imaging procedures
GE Healthcare recalls NM/CT 870 CZT system model H3906CW due to loose rotor bearing screws that may cause a bearing to release during use. Affected units have specific serial numbers listed.
GE HealthcareDec 10, 2020 - Lower riskDrug
Fresenius Kabi USA, LLC recalls Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection, USP), 0.5%, 150 mg per 30 mL (5 mg per mL), 30 mL Single
Fresenius Kabi recalls Sensorcaine-MPF injections with low epinephrine levels that may cause ineffective anesthesia. Patients should contact their doctor for alternatives.
Fresenius KabiDec 10, 2020 - Use cautionConsumer product
Thermo Tents Recalls Mór Series Tents Due to Fire Hazard; Tents are Mislabeled as Fire Retardant (Recall Alert)
Recalled Crua Mór Series tents (Crua Tri, Loj, Cottage) are mislabeled as fire retardant. Consumers must stop using near flames and replace labels with new non-fire-retardant labels to prevent fire hazards.
Crua OutdoorsDec 10, 2020 - Stop using nowConsumer product
Scentsy Recalls Electrical Oil Warmers Due to Fire Hazard (Recall Alert)
Scentsy recalls Luminary Jack and Bless This Home oil warmers due to fire hazards from corroded electrical components. Stop using immediately for a refund.
ScentsyDec 10, 2020 - Stop using nowConsumer product
Homfa Cabinets Recalled Due to Tip-Over and Entrapment Hazards; Made by Shenzhen Luosi Ge Trading Co. (Recall Alert)
Homfa recalls HPB-087 and HPB-106 cabinets due to tip-over risks. Stop use, return drawer slides for refund, and discard the rest.
HomfaDec 10, 2020 - Use cautionVehicle
JAGUAR XJ (2011) recall — Air Bags
Jaguar recalls 2010-2011 XJ vehicles with faulty air bag software that may not deploy properly in frontal crashes. Owners must contact Jaguar for free RCM software updates.
JaguarDec 9, 2020 - Lower riskMedical device
Becton Dickinson & Company recalls BD Regional Block Needles 22G x 1.50in (50 units/cs.). Indicated for administration of medications to affect anesthesia
Becton Dickinson recalls 50-unit packs of 22G regional block needles for updated safety instructions to prevent medication errors during anesthesia procedures.
Becton DickinsonDec 9, 2020 - Use cautionMedical device
Riverpoint Medical, LLC recalls Covidien CV-9590 Velosorb Fast Braided Fast absorbable Suture 14 Metric 36" 90 cm, GS-24 Taper 1/2 40 mm, undyed, UDI:
Riverpoint Medical recalls Covidien CV-9590 Velosorb sutures with potential weak strength that could cause breaks during surgery or wound separation. Affected units have specific lot numbers and sizes.
Riverpoint MedicalDec 9, 2020 - UnratedDrug
Morton Grove Pharmaceuticals, Inc. recalls Hydroxyzine Hydrochloride Oral Solution, USP (Syrup), 10 mg/5 mL, packaged in a) 4 fl oz (118 mL) bottle, NDC
Morton Grove Pharmaceuticals recalls Hydroxyzine syrup due to impurities that may cause health risks. Affected lots have specific expiration dates and NDC numbers.
Morton Grove PharmaceuticalsDec 9, 2020 - UnratedDrug
Akebia Therapeutics dba Keryx Biopharmaceutials, Inc recalls Auryxia (ferric citrate) tablets, 210 mg, 200-count bottles, Rx only, Manufactured for and distributed by: KERYX
Keryx Biopharmaceuticals recalls 200-count Auryxia (ferric citrate) tablets with CGMP deviations. This prescription medication may have manufacturing issues affecting quality.
KeryxDec 9, 2020 - UnratedDrug
Biogen MA Inc. recalls Vumerity (diroximel fumarate) delayed-release capsule, 231 mg, packaged in a) 106-count bottle, b)120-count bottle, Rx
Biogen recalls Vumerity (diroximel fumarate) 231mg capsules due to failed dissolution testing. Affected bottles: 106-count and 120-count, Rx only. No remedy specified in recall notice.
BiogenDec 9, 2020 - Stop using nowConsumer product
Washington Shoe Company Recalls Western Chief Toddler Boots Due to Choking Hazard; Sold Exclusively at Target
Western Chief recalls toddler light-up rain boots due to choking hazard. Rivets can detach. Stop use and return to Target for a refund.
Western ChiefDec 9, 2020 - Stop using nowConsumer product
Spirit Halloween Recalls Children's Flashlights Due to Fire and Burn Hazards
Spirit Halloween recalls children's flashlights with batteries that can overheat, causing burns and fires. Consumers should stop using, remove batteries, and get a refund.
Spirit HalloweenDec 9, 2020 - Stop using nowConsumer product
Neptune Benson Recalls Delta Ultra-Violet Generators For Pools and Spas Due to Fire Hazard
Neptune Benson recalls Delta UV EA-4H-10 pool UV generators due to fire risk from water leaks causing overheating at power connections. Unplug and contact for free repair or replacement.
Neptune BensonDec 9, 2020 - Stop using nowConsumer product
L G Sourcing Recalls to Repair Electric Fireplaces Due to Fire Hazard; Sold Exclusively at Lowe's Stores
Allen + Roth 62-inch electric fireplaces recalled due to fire hazard from overheating wiring connectors. Consumers must stop using and contact LG Sourcing for free repair.
allen + rothDec 9, 2020 - Stop using nowConsumer product
GrillBlazer Recalls Propane Torch Guns Due to Fire Hazard
GrillBlazer recalls Su-VGun and GrillGun propane torch guns due to propane gas leaks causing fire hazards. Consumers must stop using and contact for free repair or replacement.
GrillBlazerDec 9, 2020 - Stop using nowConsumer product
Goal Zero Recalls Power Supplies Due to Fire Hazard
Goal Zero recalls Yeti 25A Fast Charge power supplies with model 98080 due to fire risk from loose connections. Consumers must stop using and contact for free repair.
Goal ZeroDec 9, 2020 - Stop using nowConsumer product
Fiskars Brands Recalls 16 Foot Pole Saw/Pruners Due to Laceration Hazard
Fiskars recalls 16-foot pole saws/pruners with model numbers 9463, 9440, 9441 due to telescoping poles separating and causing lacerations. Consumers must stop using and return for refund.
FiskarsDec 9, 2020 - Stop using nowConsumer product
Burley Recalls Child Bicycle Seats Due to Crash Hazard
Burley recalls Dash X FM child bicycle seats due to a crash hazard. Stop using immediately and contact Burley for a free replacement.
BurleyDec 9, 2020 - Stop using nowConsumer product
Black & Decker Recalls CRAFTSMAN 10-Inch Corded Chain Saws Due to Laceration Hazard
Black & Decker recalls Craftsman 10-inch corded chain saws with extension poles that can start unexpectedly when the cord adaptor is upside down, posing laceration risk. Affected models have date codes 2019-40 to 2020-35.
CraftsmanDec 9, 2020
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