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- Use cautionMedical device
Transonic Systems Inc recalls Transonic ADT1018 Flow QC Clear Advantage Tubing, Catalog No. ADT1018, ADT1018-40 The device is indicated for use as
Transonic recalls ADT1018 Flow QC Clear Advantage Tubing (Lots B151130E2, B161115E0) due to potential infection risk from unsterile device. Affected hemodialysis patients should contact Transonic for details.
TransonicFeb 15, 2018 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls SOMATOM Spirit Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission
Siemens recalls SOMATOM Spirit CT scanners that may calculate incorrect radiation doses for head scans, potentially leading to unnecessary exposure. Affected units may need correction to ensure safe imaging.
SiemensFeb 15, 2018 - Lower riskDrug
Apollo Care recalls Vancomycin 1g added to 250mL of 0.9% Sodium Chloride IV bag, Rx only, APOLLOcare, 3801 Mojave Ct., Suite 101, Columbia,
Apollo Care recalls Vancomycin 1g IV bags due to stability concerns beyond 90 days from use date. This affects prescription-only products sold in Columbia, MO. Contact for details.
Apollo CareFeb 15, 2018 - Use cautionDrug
Medline Industries Inc recalls PVP Scrub Solution, Povidone Iodine, 7.5% (equivalent to 0.75% available iodine), 4 FL OZ bottle, Manufactured in USA
Medline recalls 67,104 bottles of PVP Scrub Solution because the iodine content may be lower than labeled. Check your lot number.
MedlineFeb 15, 2018 - Lower riskFood
Seggiano Usa Inc. recalls Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g, 7.1 oz, packaged in Glass jar, UPC Code: 812603020381
Seggiano Artichoke & Garlic Sauce & Spread (200g) was mislabeled as不含 cashews, containing undeclared cashews. Consumers should check UPC 812603020381.
SeggianoFeb 15, 2018 - Stop using nowConsumer product
Specialized Bicycle Components Recalls Bicycles Due to Crash Hazard
Specialized recalls 2018 Allez road bikes due to fork breakage causing crashes. Affected models include Allez Base, Sport, and Elite with specific color combinations. Consumers must stop using and get a free fork replacement.
SpecializedFeb 15, 2018 - Stop using nowConsumer product
Rural King Recalls Electric Blankets and Throws Due to Fire and Burn Hazards
Rural King recalls electric heated blankets and throws with fire and burn risks due to overheating cords. Affected models sold in cream and brown colors, sizes 50x60 and 84x90 inches. Customers should stop using and get a refund.
Rural KingFeb 15, 2018 - Use cautionMeat & poultry
Saker ShopRites, Inc. Recalls Empanadas due to Misbranding and an Undeclared Allergen
USDA FSIS recalls 19,757 pounds of pork and chicken empanadas due to undeclared egg allergen. Consumers urged not to consume; products should be thrown away or returned for refund.
Saker ShopRitesFeb 14, 2018 - Use cautionMeat & poultry
FSIS Issues Public Health Alert For Poultry Products due to Possible Salmonella Contamination
FSIS recalls Fareway chicken salad products sold in Iowa, Illinois, Minnesota, Nebraska, and South Dakota from Dec. 15, 2017 to Feb. 13, 2018 due to possible Salmonella contamination. Consumers are urged not to consume these products.
FarewayFeb 14, 2018 - Use cautionVehicle
LEXUS RC F (2017) recall — Fuel System, Gasoline
Toyota is recalling 2017 Lexus RC F vehicles with a fuel pump cover crack risk. This could cause fuel leaks near ignition sources, increasing fire risk. Owners must get free fuel pump replacements by April 2018.
LexusFeb 14, 2018 - Use cautionVehicle
TOYOTA CAMRY (2018) recall — Fuel System, Gasoline
Toyota is recalling 2018 Camry vehicles with V6 engines due to potential fuel leaks from improperly connected fuel pipes, which could cause fire if near ignition sources. Owners should contact Toyota for free repairs.
ToyotaFeb 14, 2018 - Use cautionVehicle
LANCE 2295 (2018) recall — Equipment
Lance is recalling certain 2018 recreational trailers with Smart-Jack power tongue jacks due to risk of unintentional retraction or extension causing injury or crash. Owners must return the jack for free replacement.
LanceFeb 14, 2018 - Use cautionMedical device
Brainlab AG recalls ExacTrac versions 6.5 through 6.5 intended to be used to place patients at an accurately defined point within the
Brainlab recalls ExacTrac software versions 6.0-6.5 for possible misinterpretation of beam authorization when used with certain radiation therapy systems, requiring users to follow specific safety steps.
BrainlabFeb 14, 2018 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls PRIMUS HI, Digital Linear Accelerator, Model No. 04504200 Product Usage: The intended use of the device is to deliver
Siemens recalls PRIMUS HI digital linear accelerators with model 0450420: updated software reduces collision risk during automatic cancer treatment movements. Affected units have specific serial numbers.
Siemens Medical SolutionsFeb 14, 2018 - Lower riskDrug
LEADIANT BIOSCIENCES, INC recalls Cystaran (cysteamine ophthalmic solution) 0.44%, 15 mL bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co. Inc.,
Leadiant Biosciences recalls Cystaran 0.44% ophthalmic solution due to subpotent cysteamine hydrochloride. Affected units have specific NDC and lot numbers. Contact for remedy details.
Leadi:ant BiosciencesFeb 14, 2018 - Stop using nowDrug
Bella All Natural recalls Bella Capsules, 600mg, 30-count bottles, Manufactured for: Bella All Natural 304 E 11th Street, Los Angeles, CA 90015
Bella All Natural recalls 32 bottles of Bella Capsules 600mg due to undeclared sibutramine. Check your lot number and expiration date for details.
Bella All NaturalFeb 14, 2018 - UnratedDrug
Fagron, Inc recalls SyrSpend SF Suspending Base, a) 500 mL (NDC 51552-1079-5) and b) 4 L (NDC 51552-1079-9), Rx Only, Manufactured by
Fagron recalls SyrSpend SF Suspending Base (500mL and 4L) due to yeast and mold contamination. This drug product poses a microbial risk to patients using it for medical purposes.
FagronFeb 14, 2018 - Lower riskFood
Springside Cheese Corp recalls Springside Monterey Jack Caribbean Red Hot Cheese Packaged in the following sizes: Net Wt. 1 lb. and 40 lbs.
Springside Cheese Corp recalls Monterey Jack Caribbean Red Hot Cheese (1 lb and 40 lb packages) due to potential pasteurization issue with milk. Consumers should check lot numbers and contact the company for details.
Springside Cheese CorpFeb 14, 2018 - Stop using nowConsumer product
ISO Beauty Recalls Hair Dryers Due to Burn Hazard
ISO Beauty recalls Ionic Pro 2000 and 2000W hair dryers due to brittle cord near base causing burn hazards. Affected units sold in multiple colors with model HD-1820.
ISO BeautyFeb 14, 2018 - Lower riskMedical device
Inpeco S.A. recalls FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2), Laboratory Automation System
Inpeco recalls specific lab equipment models due to potential freezing of modules without warning, which may delay test results for patients. Affected units include FlexLab (FLX), Accelerator a3600 (ACP), and Aptio Automation (AP2) with listed serial numbers.
InpecoFeb 13, 2018 - Lower riskMedical device
Stanbio Laboratory, LP recalls RaPET¿ RF Latex Reagent used as a component in the following kits: RaPET RF (1155-100, Control# 173201 expiry
Stanbio recalls RaPET RF Latex Reagent used in rheumatoid arthritis tests due to weakly positive results in patient serum samples. Affected kits include RaPET RF (1155-100) and others with specific expiry dates.
StanbioFeb 13, 2018 - Use cautionMedical device
Michigan Instruments, Inc. recalls Thumper Cardiopulmonary Resuscitator, Model 1007CCV, Catalog No. 15370 Product Usage: The device is used to perform
Michigan Instruments recalls Thumper Cardiopulmonary Resuscitator Model 1007CCV due to potential failure in delivering consistent chest compression depth during CPR. Affected units sold from 2017-2018.
Michigan InstrumentsFeb 13, 2018 - Lower riskMedical device
Tosoh Bioscience Inc recalls ST AIA-PACK¿ PROG III, Progesterone III Assay, Part Number: 025240
Tosoh Bioscience recalls ST AIA-PACK PROG III assay (part 025240) due to false high progesterone readings from DHEA-S cross-reactivity. Affected units may give inaccurate test results.
Tosoh Biosc: IncFeb 13, 2018 - Lower riskMedical device
Becton Dickinson & Company recalls BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5.0ml PLBL Gold, Catalog No. 367986
Becton Dickinson recalls BD VACUTAINER PLUS SST Tubes with HEMOGARD closure 13x100mm 5.0ml PLBL Gold (Catalog 367986) due to risk of stopper detachment. Affected units have specific lot numbers and expiration dates.
Becton DickinsonFeb 13, 2018 - Lower riskMedical device
Pentax of America Inc recalls Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled: 04961333232420) These instruments are
Pentax recalls ED-3490TK duodenoscopes due to potential infection risk from outdated design. Replace with updated model per manufacturer instructions.
PentaxFeb 13, 2018 - Lower riskDrug
Nostrum Laboratories Inc recalls Calcium Acetate Capsules, 667 mg, 200 Capsules per bottle, Rx Only. Manufactured by Nostrum Laboratories, Inc. Kansas
Nostrum Laboratories recalls 667mg Calcium Acetate Capsules (Rx Only) due to foreign tablets. This prescription medication may contain unsafe materials.
Nostrum LaboratoriesFeb 13, 2018 - Lower riskDrug
Hetero Labs Limited Unit V recalls Valacyclovir Tablets USP 1 gram, 30-count bottle, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ
Hetero Labs Limited recalls Valacyclovir 1g tablets due to potential temperature exposure during shipping. This may affect safety if stored improperly. Check your NDC # 31722-705-30 and lot number.
Hetero Labs LimitedFeb 13, 2018 - Stop using nowConsumer product
West Elm Recalls Glass Tables Due to Risk of Injury (Recall Alert)
West Elm recalls Jensen rectangular glass tables with SKU 4737003 or 7912629 due to unexpected shattering that could cause lacerations. Consumers must stop using and get a free replacement.
West ElmFeb 13, 2018 - Stop using nowConsumer product
Tea Collection Recalls Children's Rompers Due to Choking Hazard
Tea Living is recalling two styles of children's rompers (sizes 0-3m and 18-2:24m) due to snaps near the collar that can detach, posing a choking hazard to young children. Consumers should stop using and contact for a full refund.
Tea LivingFeb 13, 2018 - UnratedMedical device
Mesa Laboratories Bozeman Manufacturing Facility recalls SporAmpule Biological Indicator Catalog Number SPS5-100
Mesa Laboratories recalls SporAmpule Biological Indicator (SPS5-100) lots SPS-696, SPS-697, SPS-698 due to bromocresol purple concentration not meeting specifications. Affected users should contact Mesa Laboratories for details.
Mesa LaboratoriesFeb 12, 2018
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