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
35,021 found- Lower riskFood
Art Of Tea recalls Art Of Tea - Feel Better tea; Produced and Distributed by: Art of Tea LLC, Monterey Park, CA Directions: 1 Tbsp of tea
Art Of Tea recalls Feel Better tea products due to potential Salmonella contamination from supplier. Consumers should check product labels for affected SKUs and lot numbers.
Art Of TeaOct 28, 2020 - Stop using nowFood
Russ Davis Wholesale, LLC recalls J&O Mixed Veggie Cup with Dip, Net Weight 5.0 oz. (128 g), UPC 95631-85818. Mfg By: RDW, Pueblo CO 81001
Russ Davis Wholesale recalls J&O Mixed Veggie Cup with Dip due to undeclared egg. Check your UPC and sell-by date for details.
J&OOct 28, 2020 - Lower riskFood
National Food Trading Corporation recalls Frozen French Cut Green Beans. Packaged in 20.5 lb boxes. Expiration date 11/25/2022
National Food Trading Corporation recalls frozen green beans from 20.5 lb boxes with expiration 11/25/2022 for possible Listeria monocytogenes contamination. Consumers should check lot numbers.
National Food Trading CorporationOct 28, 2020 - Lower riskFood
Homestead Creamery, Inc. recalls Lemonade 1/2 gallon glass bottle. UPC:7525200265. "10% Real Juice Lemonade"
Homestead Creamery recalls 10% Real Juice Lemonade 1/2 gallon glass bottles (UPC 7525200265) due to possible chlorine sanitizer contamination. Consumers should check best buy dates (Dec 19-20, 2020) and contact the company for details.
Homestead CreameryOct 28, 2020 - Stop using nowConsumer product
Schneider Electric Recalls Surgeloc™ Surge Protection Devices Due to Fire Hazard
Schneider Electric recalls Surgeloc surge protectors from 2013-2020 due to fire risk. Affected devices have green plastic rimmed meters and specific catalog numbers. Consumers must stop using and get free replacements.
Schneider ElectricOct 28, 2020 - Lower riskConsumer product
Porter World Trade Recalls Ron Jon Surf Shop Sippy Cup Due to Violations of Federal Lead Content and Phthalates Bans
Porter World Trade recalls 13.5-ounce Ron Jon Surf Shop Sippy Cups due to lead and banned phthalates exceeding federal limits. These toxins can harm children's health if ingested.
Ron Jon Surf ShopOct 28, 2020 - Use cautionVehicle
WINNEBAGO ERA (2017) recall — Seat Belts
Winnebago recalls 2012-2021 Era 170X vehicles with seat belt upper anchorage that may not protect passengers in crashes. Owners must have seat belt inspected and fixed free of charge by dealers.
WinnebagoOct 27, 2020 - Use cautionVehicle
JEEP CHEROKEE (2021) recall — Suspension
Chrysler recalls 2021 Jeep Cherokee Latitude/Limited models due to potential front lower control arm fracture causing loss of steering control. Owners must have vehicles inspected by dealers for free replacement.
ChryslerOct 27, 2020 - Use cautionVehicle
FREIGHTLINER CASCADIA (2020) recall — Suspension
Daimler Trucks North America recalls 2020-2021 Freightliner Cascadia and related trucks for potential wheel separation due to missing or improperly installed snap rings.
DTNAOct 27, 2020 - Use cautionVehicle
AUDI Q7 (2020) recall — Structure
Audi is recalling certain 2018-2020 Q7 models due to potential head injury risk from C-pillar padding in crashes. Owners must have C-pillar deformation elements replaced at dealerships.
AudiOct 27, 2020 - Use cautionMedical device
Mani, Inc. - Kiyohara Facility recalls MANI Infusion Cannula 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials
Mani recalls 23G S infusion cannulas for eye surgery due to potential fluid leakage and disconnection risks. Affected units have specific lot codes and expiration dates.
ManiOct 27, 2020 - Lower riskMedical device
Philips Ultrasound Inc recalls All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G, EPIC 5C, EPIQ 5W, EPIQ 7G, EPIC 7C, EPIQ 7W, EPIQ
Philips recalls EPIQ and Affiniti ultrasound systems with certain software versions due to potential incorrect patient data display and saving. Affected models include EPIQ 5G, EPIQ 7G, Affiniti 30, 50, and 70. No immediate action required but check software versions.
PhilipsOct 27, 2020 - Lower riskMedical device
GE Healthcare, LLC recalls MAC VU360, Electrocardiograph
GE Healthcare recalls MAC VU36: Electrocardiograph model 2030360 001 due to incorrect patient identification and demographic errors. Affected users should contact GE Healthcare for details.
GE HealthcareOct 27, 2020 - UnratedDrug
Zydus Pharmaceuticals (USA) Inc recalls Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg, 100-count carton (10 x10 unit-dose), Rx only,
Zydus Pharmaceuticals recalls 15mg Lansoprazole Delayed-Release tablets due to failed dissolution specification. Rx-only product with NDC 68382-771-77, lot M005681, exp 3/2022. No specific remedy stated in recall notice.
Zydus PharmaceuticalsOct 27, 2020 - UnratedDrug
Sunstar Americas, Inc. recalls Paroex (chlorhexidine gluconate) Oral Rinse, USP 0.12%, Alcohol Free, Rx only, packaged in: a) 1 pint (473 mL) NDC
Sunstar recalls Paroex (chlorhexidine gluconate) oral rinse due to Burkholderia lata contamination. This prescription rinse may cause infection if used. Consumers should contact Sunstar for details.
SunstarOct 27, 2020 - Lower riskFood
CELTRADE CANADA recalls Pacific Jade Indian Curry Sauce Starter With Fenugreek and Cardamom, wholesale case with 2, 39 oz. plastic tubs, case
CELTRADE Canada recalls Pacific Jade Indian Curry Sauce Starter with Fenugreek and Cardamom due to incorrect anchovy ingredient listed on shipping case. This mismatch may cause confusion about product contents.
CELTRADEOct 27, 2020 - Lower riskFood
Vitamin Cottage Natural Foods Market, Inc DBA Natural Grocers recalls Natural Grocers, Elderberries Whole Organic, 4 oz. (113g), plastic bag, UPC 0-0082-00304-3
Natural Grocers recalls elderberry products due to potential Salmonella contamination. Consumers should check product codes and follow safety steps.
Natural GrocersOct 27, 2020 - Lower riskFood
Whole Foods Market recalls Fried Chicken Meal with Mac & Cheese, packaged in clear plastic container with printed label product code begins with
Whole Foods Market recalls Fried Chicken Meal with Mac & Cheese products with potential undeclared egg. Check product codes beginning with 247257 or 237444 for affected items.
Whole Foods MarketOct 27, 2020 - Use cautionVehicle
FOREST RIVER CARDINAL (2021) recall — Equipment
Forest River recalls 2021 Cardinal trailers due to short furnace intake sleeve causing carbon monoxide poisoning risk. Owners must have intake sleeve installed by dealers to prevent exhaust from entering the trailer.
Forest RiverOct 26, 2020 - Use cautionVehicle
FOREST RIVER CHEROKEE (2020) recall — Electrical System
Forest River recalls 2019-2021 Cherokee trailers due to potential fire risk from poor electrical connections. Owners must contact customer service for free repairs.
Forest RiverOct 26, 2020 - Use cautionVehicle
FOREST RIVER PALOMINO (2020) recall — Equipment
Forest River recalls 2019-2021 Palomino trailers due to antenna that may detach while moving, creating road hazards. Owners should contact customer service for free repair or replacement.
Forest RiverOct 26, 2020 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica IM 1300 Analyzer - Product Usage: automated, immunoassay analyzers designed to perform in vitro diagnostic
Siemens recalls Atellica IM 1300 analyzers with software version V1.23.1 or lower that may reset custom settings causing false test results. Affected units have Siemens Material Number 11066001.
Siemens HealthcareOct 26, 2020 - Lower riskDrug
Ascent Pharmaceuticals, Inc. recalls Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325mg 100-count bottles, Rx Only, Manufactured for : Camber
Ascent Pharmaceuticals recalls 100-count hydrocodone/acetaminophen tablets with foreign losartan tablets. Consumers should check product details and contact the company for guidance.
Ascent PharmaceuticalsOct 26, 2020 - Lower riskDrug
Jubilant Cadista Pharmaceuticals, Inc. recalls Olanzapine Orally Disintegrating Tablets, 5 mg, 30 count (3x10 unit dose) blister pack, Rx only, Manufactured by:
Jubilant Cadista Pharmaceuticals recalls 5mg Olanzapine orally disintegrating tablets due to subpotent risk. This may affect prescription medication safety. Contact for details.
Jubil: CadistaOct 26, 2020 - Lower riskFood
Sunnyside Farms recalls Dole Brands, Savory Spinach Dijon, 4.9 oz,
Sunnyside Farms recalls Dole Brands Savory Spinach Dijon salad due to mislabeled product with incorrect 'Candied Walnut Salad' on top label. Check labels for 4.9oz, 6 or 8 per case.
Sunnyside FarmsOct 26, 2020 - Lower riskMedical device
Ethicon, Inc. recalls PROCEED Surgical Mesh Hernia Mesh Oval, 15 cm x 20 cm
Ethicon recalls hernia mesh oval (15cm x 20cm) due to hair found in packaging. Consumers should check product codes and contact Ethicon for details.
EthiconOct 23, 2020 - Use cautionMedical device
Becton Dickinson & Company recalls BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for parenteral administration of a drug from a cartridge
Becton Dickinson recalls BD Ultra-Fine Pen Needles due to incorrect labeling. The cartons are labeled for the Latin American market, missing US compatibility info.
BDOct 23, 2020 - Use cautionMedical device
HUBO INTERNATIONAL INC recalls VGlove NITRILE *** Protect Your Life 100 Patient examination gloves
HUBO International recalls 100-patient examination gloves labeled as nitrile but contain latex. This poses allergy risks for sensitive users. Stop using immediately to avoid allergic reactions.
HUBOOct 23, 2020 - Stop using nowMedical device
Biomeme, Inc. recalls The Biomeme SARS-CoV-2 Real-Time RT-PCR Test is a molecular in vitro diagnostic test that is based on widely used
Biomeme recalls its SARS-CoV-2 test due to false positive results from software errors. Users should stop using the test immediately to avoid incorrect health decisions.
BiomemeOct 23, 2020 - UnratedMedical device
Coloplast Manufacturing US, LLC recalls Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are
Coloplast recalls Titan Pump devices for men with erectile dysfunction implants due to potential increased fracture risk over time. No remedy specified in official notice.
ColoplastOct 23, 2020
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