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
34,956 found- Use cautionVehicle
JEEP GRAND CHEROKEE (2018) recall — Equipment
Chrysler recalls 2018 Jeep Grand Cherokee floor mats that may stick accelerator pedal, causing crash risk. Owners must replace mats free of charge by November 15, 2018.
ChryslerOct 29, 2018 - Use cautionVehicle
JEEP GRAND CHEROKEE (2018) recall — Equipment
Chrysler recalls 2018 Jeep Grand Cherokee models with floor mats that may prevent accelerator pedal from returning to idle, risking crashes. Owners must replace mats free of charge by November 15, 2018.
ChryslerOct 29, 2018 - Use cautionVehicle
HEARTLAND PIONEER (2019) recall — Equipment
Heartland is recalling 2019 Pioneer trailers with a flexible LP hose that can overheat and cause fire. Owners must replace with rigid metal hose.
HeartlandOct 29, 2018 - UnratedDrug
Akorn, Inc. recalls Clindamycin Phosphate Topical Solution USP, 1% (10 mg/mL clindamycin), 60 pledget applicators per jar, Rx only.
Akorn recalls Clindamycin Phosphate Topical Solution 1% (Rx only) due to impurities. Products with NDC 61748-0201-60 and specific lot numbers from 2018-2019 are affected. No remedy provided in official notice.
AkornOct 29, 2018 - Stop using nowDrug
Westminster Pharmaceuticals Llc recalls Westminster Irbesartan Tablets, USP 75 mg Rx Only Manufactured by: ScieGen Pharmaceuticals, Inc. Hauppauge, NY 11788
Westminster Pharmaceuticals recalls 75mg Irbesartan tablets with traces of NDEA impurity found in specific batches. FDA testing confirmed contamination in certain lots.
Westminster PharmaceuticalsOct 29, 2018 - Lower riskDrug
GE Healthcare Inc. Life Sciences recalls Omnipaque (iohexol) Injection, 180mgI/mL, 20 mL Single-Dose Vial, packaged in 10 x 20 mL Vials per carton, Rx only,
GE Healthcare recalls Omnipaque 180mg injection vials due to potential container defects that could compromise sterility and cause glass particles. Affected products include specific lot numbers and packaging.
GE HealthcareOct 29, 2018 - UnratedDrug
Sciegen Pharmaceuticals Inc recalls Westminister Irbesartan Tablets, USP, 75 mg (a) 30-count bottle (NDC 69367-119-01), (b) 90-count bottle (NDC
Sciegen Pharmaceuticals recalls Westminster Irbesartan 75mg tablets due to FDA-confirmed NDEA impurity. Stop using affected bottles immediately.
Sciegen PharmaceuticalsOct 29, 2018 - Stop using nowFood
J&J Snack Foods Handheld Corp recalls Fit & Active Southwest Veggie Stuffed Sandwiches NET WT 9 oz (255 g) KEEP FROZEN Distributed by ALDI Inc. Batavia, IL
ALDI distributes Fit & Active Southwest Veggie Stuffed Sandwiches recalled due to possible Listeria and Salmonella contamination. Check your freezer.
Fit & ActiveOct 29, 2018 - Lower riskFood
Feast Mode Blending & Filling recalls Feast Mode Flavors Garlic Beer Seasoning, Nt. Wt. 5 oz, plastic bottles
Feast Mode Blending & Filling recalls Garlic Beer Seasoning (5oz plastic bottles) due to being mislabeled as gluten-free. Consumers should check labels for accurate allergen information.
Feast Mode Blending & FillingOct 28, 2018 - Lower riskMeat & poultry
Red Square Foods, Inc., Recalls Frozen Not-Ready-To-Eat Meat and Poultry Products due to Misbranding and Undeclared Allergens
Red Square Foods recalls frozen meat and poultry products due to undeclared allergens like eggs, milk, and wheat. Consumers are urged not to consume these products and should discard or return them.
Red Square FoodsOct 27, 2018 - Use cautionMeat & poultry
Suzanna's Kitchen, Inc., Recalls Poultry Products due to an Unapproved Substance
USDA FSIS recalls 15,408 pounds of Suzanna's Kitchen organic gluten-free grilled chicken strips due to thallium contamination. Consumers urged not to consume or dispose of recalled products.
Suzanna's KitchenOct 26, 2018 - Use cautionVehicle
PIERCE SABER (2017) recall — Exterior Lighting
Pierce is recalling 2017-2018 models with Whelen brake lights that may illuminate without braking, risking crashes. Owners must contact Pierce for free brake light replacement.
PierceOct 26, 2018 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis Zee and Zeego, model no. 10272462 AXIOM Artis zee/Zeego is a family of dedicated angiography systems developed
Siemens recalls Artis Zee and Zeego angiography systems with serial numbers 910045-09 to 911354-27 due to possible cooling hose leaks causing overheating and potential procedure delays.
SiemensOct 26, 2018 - Lower riskMedical device
Merit Medical Systems, Inc. recalls Custom Procedure Kit, Custom Kit, REF/Product Code: K12T-03688, single use, RX Only, Sterile EO, LATEX FREE, UDI:
Merit Medical recalls Custom Procedure Kit (K12T-03688) due to incorrect latex labeling. This may cause confusion about whether the kit is latex-free, but does not pose a safety risk.
Merit Medical SystemsOct 26, 2018 - Lower riskMedical device
Implant Direct Sybron Manufacturing, LLC recalls Implant Direct, REF654311U, simply InterActive Implant, Surface: SBM, Qty 1, 4.3mmD x 11.5mmL, 3.4mmD Platform, RX
Implant Direct recalls specific dental implants due to possible packaging error with incorrect healing collar. Affected units include REF654311U, SBM surface, 4.3mmD x 11.5mmL, sterile. No remedy stated in official notice.
Implant DirectOct 26, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Levetiracetam in 0.54 % Sodium Chloride Injection 1,500/mg/100mL (15mg/mL), For intravenous Infusion Only, 1 x 100 mL
Dr. Reddy's recalls Levetiracetam injection due to label error showing incorrect strength. The product may be mislabeled as 0.75% Sodium Chloride (1000 mg/100 mL) when it's actually 0.54% Sodium Chloride (1500 mg/100 mL).
Dr. Reddy'sOct 26, 2018 - UnratedDrug
RemedyRepack Inc. recalls Metoprolol Tartrate Injection, USP 5mg/5mL, vials, Rx only, MFG: Claris Lifesciences Inc., North Brunswick, NJ 08902,
RemedyRePack recalls Metoprolol Tartrate Injection vials due to pH instability. This may affect medication safety. Check your vial lot numbers for affected batches.
RemedyRePackOct 26, 2018 - Use cautionDrug
S.C. Johnson Professional recalls Alcohol Free Foaming Hand Sanitizer (benzalkonium chloride), 0.13%, 1 L (33.8 fl. oz.) cartridge packaged in 8
S.C. Johnson Professional recalls Alcohol Free Foaming Hand Sanitizer cartridges due to manufacturing deviations before microbiological testing.
S.C. Johnson ProfessionalOct 26, 2018 - Lower riskFood
Maribel's Sweets, Inc. recalls Cacao Market by MarieBelle Rosemary Truffle Salt 60% Dark Chocolate Bar, NET WT. 2.8 oz. (80g). UPC code: 877708004841.
Maribel's Sweets recalls 60% dark chocolate bars containing undeclared milk. Consumers should check UPC 877708004841 for affected products.
Maribel's SweetsOct 26, 2018 - Stop using nowConsumer product
Children's Toy Instrument Sets Recalled Due to Violation of the Federal Lead Paint Ban; Made by Creative Sto and Sold Exclusively at Amazon.com (Recall Alert)
Creative Sto recalls INNOCHEER children's musical instrument sets due to lead paint exceeding federal safety limits. Lead ingestion risks health issues for young children. Consumers should stop using and return items for refund.
Creative StoOct 26, 2018 - Lower riskMeat & poultry
Recall Notification Report 104-2018 (Smoked Whole Chicken Products)
All Peoples Food recalls ~3,904 lbs of smoked whole chicken due to undeclared MSG. Check your freezer for bulk boxes produced Sept 4-25, 2018.
All Peoples FoodOct 25, 2018 - Use cautionVehicle
BMW X3 (2017) recall — Engine And Engine Cooling
BMW is recalling certain 2017 X3 models with a risk of fire due to melting intake manifold from EGR cooler leaks. Owners must contact BMW for free repairs.
BMWOct 25, 2018 - Use cautionVehicle
KIA STINGER (2018) recall — Electrical System
Kia recalls 2018 Stinger vehicles with damaged wiring harness that could cause fire. Owners must have wiring inspected by dealers; free repairs if needed. Recall started December 20, 2018.
KiaOct 25, 2018 - Use cautionVehicle
TOYOTA 4RUNNER (2019) recall — Equipment
Southeast Toyota is recalling certain 2017-2019 Toyota 4Runners with TRD wheel packages due to potential incorrect Gross Vehicle Weight Rating labels, which could lead to vehicle overload and crash risk.
Southeast ToyotaOct 25, 2018 - Use cautionVehicle
FOREST RIVER CHEROKEE (2019) recall — Equipment
Forest River recalls 2018-2019 Cherokee Alpha Wolf and Arctic Wolf trailers due to potential awning arm detachment causing injury or crash risk. Owners must have awnings inspected and fasteners replaced free of charge.
Forest RiverOct 25, 2018 - Lower riskMedical device
The Magstim Company Limited recalls HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
Magstim recalls HORIZON Ez Arm devices with specific serial numbers due to potential stray stainless-steel cable protrusion from heat shrink sleeving.
MagstimOct 25, 2018 - Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO 10000-USA#QUADROX-i Neo.+Reservoir), Part
Maquet recalls Quadrox-i Neonatal without integrated arterial filter and VHK 11000 units with potential blood leakage at blood inlet connector using reducing screw adapter 1/4 x 3/16.
MaquetOct 25, 2018 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci SP Instrument Arm Drape. REF 430013-12 QTY 1 Pouch
Intuitive Surgical recalls da Vinci SP Instrument Arm Drape (REF 430013-12) due to potential tear during use, risking sterile barrier breaches. Affected units include all lots of this pouch.
Intuitive SurgicalOct 25, 2018 - Lower riskFood
Valley Processing Inc. recalls Apple juice concentrate and organic apple juice concentrate in 52 gallon drums, 5 gallon pails, 4 gallon pails, and 260
Valley Processing recalls apple juice concentrates with high inorganic arsenic levels. Products distributed for non-fermentation use are affected. Consumers should check lot numbers for recall.
Valley ProcessingOct 25, 2018 - Lower riskFood
Barcelona Nut Company recalls Barcelona Nut Company, Roasted and Salted Select Inshell Pistachios 21/25, flexible package, shelf life of one year.
Barcelona Nut Company recalls roasted and salted select inshell pistachios (2019) due to salmonella contamination. Consumers should avoid these products.
Barcelona Nut CompanyOct 25, 2018
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