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
Ad-Tech Medical Instrument Corporation recalls Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for the purpose of connecting these electrodes to third
Ad-Tech recalls lightweight cables with incorrect labels that could lead to improper connections. Affected items have specific lot numbers. Contact Ad-Tech for details.
Ad-TechAug 9, 2021 - Lower riskFood
Mane Inc recalls BBQ Seasoning Packaged in 50lb poly bag/cardboard box combo and kraft paper bags
Mane Inc recalls BBQ seasoning products with batch numbers 0000700205, 0000700206, and 0000682167 due to Salmonella contamination. Consumers should check their products and contact the company for details.
Mane IncAug 9, 2021 - Lower riskFood
Jimmy's Cookies, LLC recalls Marketside Chocolate Candy Cookie Cake, 24 oz. 12 x 12 black tray with clear lid.
Jimmy's Cookies recalls 24oz Marketside Chocolate Candy Cookie Cake with peanuts. Undeclared allergen poses risk for peanut allergy sufferers. No remedy specified in recall notice.
Jimmy's CookiesAug 9, 2021 - UnratedFood
CB DISTRIBUTION LLC recalls Cotton Blues Cheesecake Co. Strawberry Swirl Single Slice 6oz plastic container 36 packages per case
CB Distribution LLC recalls Cotton Blues Strawberry Swirl cheesecakes due to incorrect ingredient labeling. Check lot numbers and best-by dates.
Cotton Blues Cheesecake Co.Aug 9, 2021 - Lower riskFood
Able Groupe Inc recalls Lebenswert Anfangsmilch Stage 1 Organic Infant Milk Formula
Able Groupe recalls Lebenswert Anfangsmilch Stage : Some products may not provide enough iron for infants, especially premature or low birth weight babies. All products lack required FDA labeling.
Able GroupeAug 8, 2021 - Use cautionVehicle
BMW X5 (2019) recall — Air Bags
BMW recalls one 2019 X5 xDrive 40i vehicle due to potential passenger air bag failure in crashes. Owners must have instrument panel replaced free by dealer.
BMWAug 7, 2021 - Use cautionVehicle
BMW X4 (2019) recall — Air Bags
BMW recalls 2019 X4 models with potential front air bag deactivation during crashes. Owners must have seat foam replaced free by dealers.
BMWAug 7, 2021 - Use cautionVehicle
CHEVROLET BOLT EV (2022) recall — Air Bags
Chevrolet is recalling 2022 Bolt EVs with potentially missing or improperly tightened driver air bag fasteners. This could increase injury risk in crashes. Free repairs available.
ChevroletAug 7, 2021 - Use cautionVehicle
KIA K5 (2021) recall — Fuel System, Gasoline
Kia recalls 2021 K5 vehicles with 2.5L turbocharged engines for potential fuel leaks that could cause fire. Owners must have fuel pipe inspected or replaced at no cost by dealers.
KiaAug 7, 2021 - Use cautionVehicle
THOR MOTOR COACH ARIA (2020) recall — Structure
Thor Motor Coach is recalling certain 2020 Aria models due to adhesive failure that may cause window vents to detach, increasing crash or injury risk. Affected vehicles will receive free window inspections and repairs.
Thor Motor CoachAug 7, 2021 - Use cautionVehicle
CHRYSLER 300 (2020) recall — Visibility
Chrysler recalls 2020-2021 300 models with potential windshield detachment during crashes. Affected vehicles may not meet federal safety standards. Owners should contact FCA US LLC for free windshield sealant replacement.
ChryslerAug 7, 2021 - Lower riskFood
Gem City Fine Foods, LLC recalls Flourless Chocolate Torte, 14 oz., in recyclable plastic circular container with black base and clear lid, Gem City
Gem City Fine Foods recalls 14oz Flourless Chocolate Torte for mislabeled pecans in ingredients despite no nut use since April 2018. Consumers should check for specific batch codes.
Gem CityAug 7, 2021 - Use cautionVehicle
LAND ROVER DEFENDER (2020) recall — Exterior Lighting
Land Rover is recalling 2020 Defender models with smoked rear lights that may fail during bright conditions, risking crashes. Owners must get free light assembly replacements.
Land RoverAug 6, 2021 - Lower riskMedical device
Philips Ultrasound Inc recalls Affiniti Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: Affiniti 30 795121 Affiniti 30
Philips recalls Affiniti Diagnostic Ultrasound Systems with software versions 5.0, 5.0.1, and 5.0.2 due to intermittent lock-ups during exams. Affected models include Affiniti 30, 50, and 70 series with specific serial numbers. No action is required for users but they should check their software version.
PhilipsAug 6, 2021 - Lower riskMedical device
Smiths Medical ASD Inc. recalls NORMOFLO Irrigation Warming administration set (disposable), Models IR-40, IR-500, IR-600, IRI-600, IRI-600B, IR-700
Smiths Medical recalls NORMOFLO Irrigation Warming sets (models IR-40, IR-500, IR-600, IRI-600, IRI-600B, IR-700) due to potential aluminum leaching with blood products and longer use. Consumers should check their product codes.
Smiths MedicalAug 6, 2021 - Lower riskMedical device
Heartware, Inc. recalls Medtronic HVAD Pump Implant Kits
Heartware recalls Medtronic HVAD Pump Implant Kits (product numbers 1100-1104JP, 1205, MCS1705PU) due to potential driveline repair complications during controller exchanges.
HeartwareAug 6, 2021 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Ion Flexison Biopsy Needle, 19G, Extension Range : 0-3 cm, Ref: 490104-09 and 49004-10, 5-pack, Sterile EO, Rx only,
Intuitive Surgical recalls 5-packs of 19G Ion Flexison Biopsy Needles with potential sheath tip separation. Affected lots include S90200303 to S90210414. Contact for remedy.
Intuitive SurgicalAug 6, 2021 - Lower riskMedical device
Medline Industries Inc recalls NAMIC Stopcocks: (1) NAMIC STOPCOCK, 200 psi (14 bar), REF 70015002, UPN H965700150021, Three-way Stopcock with
Medline recalls 13 types of sterile stopcocks with potential microscopic pinholes causing non-sterile conditions. Affected models include 200 psi and 400 psi variants with specific lot numbers. Consumers should check their product details and contact Medline for replacement.
MedlineAug 6, 2021 - Lower riskMedical device
Johnson & Johnson Surgical Vision Inc recalls TECNIS Eyhance IOLs are permanent intraocular implants intended for implantation in the capsular bag. The TECNIS
Johnson & Johnson Surgical Vision recalls TECNIS Eyhance IOLs with endotoxin levels exceeding safety limits. This nonconforming product was distributed in error during cataract surgery procedures.
Johnson & Johnson Surgical VisionAug 6, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity Universal Viewer and Viewer 6.0 - Product Usage: Is a device that displays medical images (including
GE Healthcare recalls Centricity Universal Viewer and Viewer 6.0 software versions 6.0 through 6.0 SP7.1 due to image acquisition failures and synchronization issues with the Centricity Enterprise Archive.
GE HealthcareAug 6, 2021 - Lower riskMedical device
ZOLL Circulation, Inc. recalls ZOLL, REF 8700-0793-40 (SL-2593AE) SOLEX 7, Intravascular Heat Exchange Catheter Kit with central venous infusion
ZOLL recalls SOLEX 7 Intravascular Heat Exchange Catheter Kit with central venous infusion due to potential leaks from catheter or start-up kit tubing. All lots affected.
ZOLLAug 6, 2021 - Lower riskDrug
XELLIA PHARMACEUTICALS USA, LLC recalls Micafungin for Injection, 100 mg/vial, Single-Dose Vial, Sterile, Rx Only, For Intravenous Infusion Only, Manufactured
Xellia Pharmaceuticals recalls Micafungin 100mg vials due to missing critical package insert sections. This could affect patient safety information. Consumers should contact the company for details.
Xellia PharmaceuticalsAug 6, 2021 - Lower riskDrug
The Harvard Drug Group recalls Carbamazepine 200mg Tablets, USP, 200 mg, 100 Count Unit Dose Cartons, Rx only, Manufactured by: Torrent
The Harvard Drug Group recalls Carbamazepine 200mg tablets due to failed dissolution specifications. This may affect medication effectiveness. Check your product details to see if you are affected.
The Harvard Drug GroupAug 6, 2021 - Lower riskFood
Ingredion recalls Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with a net weight of 5kg each and 2.5kg sample
Ingred: Fermentation-derived pepsin products with undeclared egg allergen in 5kg and 2.5kg bags. Consumers should check packaging for model numbers 20352B1, 20352B2, etc. to determine if affected.
IngredionAug 6, 2021 - Stop using nowMeat & poultry
Blount Fine Foods Corp. Recalls Chicken Soup Products Due To Possible Foreign Matter Contamination
Blount Fine Foods recalls chicken tortilla soup products from July 2021 that may contain pieces of gray nitrile gloves. Consumers are urged not to consume these products and should discard or return them to the store.
Blount Fine FoodsAug 5, 2021 - UnratedMedical device
Beckman Coulter Inc. recalls Access SARS CoV-2 IgG (1st IS) Assay: Access Immunoassay Systems REAGENT PACK, REF C74339 Access SARS-CoV-2 IgG (1st
Beckman Coulter recalls Access SARS-CoV-2 IgG (1st IS) Assay reagents due to insufficient evidence for Emergency Use Authorization. Affected units include specific lot numbers and UDI codes.
Beckman CoulterAug 5, 2021 - Use cautionMedical device
Armstrong Medical Services Limited recalls AMSORB PLUS PREFILLED G-CAN 1.0L; Carbon dioxide absorbent canister; Product codes AMAB3801 and AMAB3801GE. Used in
Armstrong Medical recalls AMSORB PLUS PREFILLED G-CAN 1.0L carbon dioxide absorbent canisters with product codes AMAB3801 and AMAB3801GE due to potential high resistance to gas flow during anesthesia, which could delay treatment. Affected units were sold from specific production lots.
Armstrong MedicalAug 5, 2021 - Lower riskMedical device
M.D.L. S.r.l. recalls Soft Tissue Biopsy Needles
M.D.L. recalls specific soft tissue biopsy needles due to potential sterility compromise. Affected models and lot numbers listed. Consumers should check their items and contact the manufacturer for details.
M.D.L.Aug 5, 2021 - Lower riskMedical device
C.R. Bard Inc recalls Catalog A319416AM, SureStep" Foley Tray, Bardex" I.C., Complete Care", Urine Meter, Temperature Sensing, StatLock"
C.R. Bard recalls SureStep Foley Trays with potential packaging defects that could compromise sterile barrier. Affected units have specific lot numbers and expiration dates. Consumers should check their product details to determine if recalled.
BardAug 5, 2021 - Lower riskDrug
DuPont Nutrition USA, Inc recalls Avicel, Mirocrystalline cellulose, packaged in bulk as PH101 NF, PH102 NF, PH200 NF, Manufactured by: DuPont Nutrition
DuPont Nutrition recalls bulk cellulose powder PH101 NF, PH102 NF, PH200 NF due to conductivity testing failures. These excipients may not meet quality standards for pharmaceutical use.
DuPont NutritionAug 5, 2021
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