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
W.L. Gore & Associates, Inc. recalls GORE VIBIL Biliary Endoprosthesis: stents, drains and dilators for the biliary ducts. Catalogue numbers: VH1008040,
Gore recalls biliary endoprosthesis stents and drains that may be shorter than labeled, potentially causing improper placement in bile ducts. Affected units include specific catalog and serial numbers.
GoreApr 5, 2021 - Use cautionFood
REDCON1 LLC recalls MRE LITE Animal Based Protein, Oatmeal Chocolate Chip, Animal Protein Powder Drink Mix, Net Wt. 30.69 oz (1.92lb) (870g)
REDCON1 LLC recalls MRE LITE Animal Based Protein, Oatmeal Chocolate Chip flavor due to undeclared wheat and soy allergens.
REDCON1Apr 5, 2021 - Use cautionVehicle
INFINITI Q50 (2021) recall — Engine And Engine Cooling
INFINITI is recalling 2021 Q50 vehicles with potential engine stall risk from fuel supply issues. Owners will receive free software updates to prevent crashes.
INFINITIApr 4, 2021 - Use cautionVehicle
NISSAN ALTIMA (2020) recall — Steering
Nissan recalls certain 2020-2021 Altima vehicles due to potential tie rod ball joint detachment causing loss of steering control. Owners must contact Nissan for free repairs.
NissanApr 3, 2021 - Use cautionVehicle
KIA SPORTAGE (2020) recall — Service Brakes, Hydraulic
Kia recalls certain 2017-2021 Sportage vehicles due to potential engine compartment fire from electrical short circuits in brake system. Free repairs available.
KiaApr 3, 2021 - Stop using nowFood
Hi Tech Pharmaceuticals recalls ISOMORPH 28 PURE WHEY iSOLATE COOKIES N CREAM DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89836 8 & 5lb, UPC 6 49241
Hi Tech Pharmaceuticals recalls ISOMORPH 28 Whey Isolate Cookies N Cream dietary supplement due to undeclared milk, wheat, and soy. Check your UPC and expiration date.
Hi Tech PharmaceuticalsApr 3, 2021 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Raw Ground Chorizo Sausage Products Due to Possible Foreign Matter Contamination
FSIS public health alert: 39 pounds of raw ground chorizo sausage from Lonely Lane Farms may contain hard crystalline material. Do not consume these products as they should be discarded or returned.
Lonely Lane FarmsApr 2, 2021 - Stop using nowFood
Starwest Botanicals, Inc recalls Starwest Botanicals Item#: 209617-34, Item# 209617-31 Wood Betony Herb C/S Organic Stackys Officinalis Origin: Croatia
Starwest Botanicals recalls specific lots of Wood Betony Herb tea due to potential E. coli contamination. Check your lot numbers immediately.
Starwest BotanicalsApr 2, 2021 - Lower riskMeat & poultry
Rong Shing Trading Inc. Recalls Ineligible Beef Products Imported from China
USDA FSIS recalls 3,365 pounds of Chinese-style hot pot beef bases imported from ineligible country. Products contain beef tallow and must not be consumed. Consumers should discard or return items.
Rong Shing Trading Inc.Apr 1, 2021 - Lower riskMedical device
Stryker Leibinger GmbH & Co. KG recalls DirectInject consists of a sterile dual paste system which is calcium phosphate based. Upon injection through the
Stryker Leibinger recalls DirectInject cement paste system due to inability to inject paste into target location. Affected units have specific lot numbers and product codes.
Stryker Leib:ingApr 1, 2021 - Lower riskMedical device
Merits Holdings Co. dba Merits Health Products, Inc. recalls Power Wheelchair
FDA Class II recall for Merits Health Digital Thermometers (Model TMU200900766, etc.) due to potential inaccurate temperature readings. Distributed nationwide and to Canada.
Merits HealthApr 1, 2021 - Lower riskMedical device
CLINICAL LASERTHERMIA SYSTEMS AB recalls Tranberg MR Stylet, 1.8mm/15G, 230mm, REF: 4013-06, Rx Only, Sterile EO - Product Usage: used with the Tranberg¿ MR
CLINICAL LASERTHERMIA SYSTEMS AB recalls Tranberg MR Stylets (REF: 4013-06) due to potential inadequate sterilization. These single-use sterile devices may not be properly sterilized, risking infection.
CLINICAL LASERTHERMIA SYSTEMS ABApr 1, 2021 - Lower riskDrug
Jubilant Cadista Pharmaceuticals, Inc. recalls Itraconazole Capsules, 100 mg, 30-count bottles, Rx only, Manufactured by: Jubilant Generics Ltd., Roorkee - 247661,
Jubilant Cadista recalls 100mg itraconazole capsules (NDC 59746-282-30) due to failed dissolution specifications. This may affect medication effectiveness. Contact for return instructions.
Jubilant CadistaApr 1, 2021 - Stop using nowConsumer product
Infant Bath Seats Recalled Due to Drowning Hazard; Imported by BATTOP; Sold Exclusively on Amazon.com (Recall Alert)
BATTOP foldable infant bath seats (model BB2:2206) recalled due to drowning risk from tipping over. Consumers must stop using and return for full refund via Amazon.
BATTOPApr 1, 2021 - Use cautionConsumer product
doTERRA Recalls 1.3 Million Bottles of Deep Blue, PastTense, and Deep Blue Touch Essential Oils Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
doTERRA recalls 1.3 million bottles of Deep Blue, PastTense, and Deep Blue Touch essential oils due to non-child-resistant packaging, posing poisoning risk to young children. Consumers should store out of reach and contact for free replacement.
doTERRAApr 1, 2021 - Use cautionVehicle
PORSCHE MACAN (2021) recall — Suspension
Porsche recalls certain 2:021 Macan models for potential brake damage and loss of control. Affected vehicles may need suspension repairs to prevent crashes.
PorscheMar 31, 2021 - Use cautionVehicle
HARLEY-DAVIDSON XL883N (2020) recall — Exterior Lighting
Harley-Davidson recalls 2020 XL883N motorcycles with potential headlight beam failure causing reduced visibility and crash risk. Owners must get free bulb shield installed by dealers.
Harley-DavidsonMar 31, 2021 - Lower riskMedical device
Soft Computer Consultants, Inc. recalls SoftCytogenetics
Soft Computer Consultants recalls SoftCytogenetics software versions 4.1.11.20, 4:1.12.11, and 4.1.15.6 due to incorrect test results from reruns. Affected users should contact the company for details.
Soft Computer ConsultantsMar 31, 2021 - Lower riskMedical device
Smiths Medical ASD Inc. recalls ACE MDI Spacer with Small Mask - Product Usage: designed to assist with the delivery of aerosolized medications from
Smiths Medical recalls ACE MDI Spacers with Small Masks due to potential incorrect shipping box labels. This may affect product identification but does not pose a safety risk.
Smiths MedicalMar 31, 2021 - Lower riskMedical device
Soft Computer Consultants, Inc. recalls SoftGenomics version 4.1.15.6 SoftGenomics is a laboratory workflow and information management system to be used in a
Soft Computer Consultants recalls SoftGenomics version 4.1.15.6 due to software showing wrong results and PDF mismatch with HIS. Affected users should contact for remedy.
Soft Computer ConsultantsMar 31, 2021 - Lower riskMedical device
Welch Allyn Inc Mortara recalls Surveyor S12/S19 Bedside Patient Monitor, with AM12M Acquisition Module accessory. Impacted software version of the
Welch Allyn recalls Surveyor S12/S19 bedside patient monitors with AM12M acquisition module software version 1.5.1 that do not meet IEC 60601-2-27 safety standards. Affected units have specific serial numbers and part numbers listed in the recall notice.
Welch AllynMar 31, 2021 - Use cautionMedical device
Smiths Medical ASD Inc. recalls Tubing with male luer lock adapter (Component) a. 76 cm, REF 601280 b. 122 cm, REF 607281. component of extravascular
Smiths Medical recalls specific lots of tubing with male luer lock adapters due to potential insufficient welds in high-pressure adaptors, which could lead to device failure during use.
Smiths MedicalMar 31, 2021 - UnratedDrug
Apotex Corp. recalls Guanfacine Extended-Release Tablets 2 mg,100-count bottles, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario
Apotex recalls 2mg Guanfacine Extended-Release Tablets due to trace quetiapine fumarate contamination. Affected lots expire Nov 2022. No action needed per official notice.
ApotexMar 31, 2021 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Riomet (metformin hydrochloride oral solution) 500 mg/5 mL Cherry Flavor, 16 fl. oz., 473 mL bottles Rx Only,
Sun Pharmaceutical recalls Riomet (metformin hydrochloride oral solution) 500mg/5mL Cherry Flavor bottles due to microbial contamination. This poses a risk of infection from non-sterile product. Consumers should check NDC 10631-206-02 and lot numbers listed.
Sun PharmaceuticalMar 31, 2021 - UnratedDrug
QMart recalls IMPERIAL GOLD 2000, Male Sexual Performance Enhancement, 1 Capsule, UPC 718122040702
QMart recalls Imperial Gold 2000 male performance capsules due to unapproved drug ingredients. FDA found tadalafil or sildenafil without proper FDA approval.
QMartMar 31, 2021 - Use cautionVehicle
PIERCE SABER (2017) recall — Exterior Lighting
Pierce is recalling 2016-2018 Saber vehicles with bright rear LED lights that may cause crashes. Owners must install a free filter kit by April 26, 2021.
PierceMar 30, 2021 - Use cautionVehicle
ALFA ROMEO STELVIO (2021) recall — Air Bags
Chrysler is recalling 2021 Alfa Romeo Stelvio vehicles with a risk of incomplete side air bag deployment during crashes. Owners must have the air bag assembly replaced free by May 19, 2021.
Alfa RomeoMar 30, 2021 - Use cautionVehicle
LINCOLN AVIATOR (2020) recall — Back Over Prevention
Ford is recalling 2020-2021 Lincoln Aviators with backup camera issues that may cause crashes due to distorted or blank images. Owners must update software to fix the problem.
FordMar 30, 2021 - Lower riskMedical device
Omnia SRL recalls Omnia Soft Tissue Punch is a dental instrument designed to remove with precision a circular section of oral soft tissue
Omnia recalls specific dental instruments due to inadequate sterilization processes at a contracted facility since 2016, posing infection risks. Affected models and lots listed.
OmniaMar 30, 2021 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis systems - Product Usage: an angiography systems developed for single and biplane diagnostic imaging and
Siemens recalls Artis angiography systems due to corrosion from improper cleaning, which may cause C-Arm malfunctions and patient safety risks. Affected models include Artis FC, FA, MP, and others with specific serial numbers.
SiemensMar 30, 2021
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