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
34,959 found- Use cautionVehicle
NISSAN ALTIMA (2019) recall — Exterior Lighting
Nissan recalls 2019 Altima vehicles with brake lights staying on when brakes aren't pressed, which could cause crashes. Owners must contact Nissan for free brake pedal repair.
NissanMar 25, 2019 - Use cautionVehicle
DUTCHMEN KODIAK (2019) recall — Tires
Keystone is recalling 2018-2019 Dutchmen Kodiak trailers with specific tire models due to potential tire failure causing loss of vehicle control. Owners should contact customer service for a free suspension lift kit installation.
KeystoneMar 25, 2019 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2020) recall — Steering
Daimler Trucks North America recalls 2019-2020 Thomas Built Saf-T-Liner C2 school buses with potential steering assist loss due to hose clamp issues. Affected vehicles may need immediate inspection and repair.
Thomas BuiltMar 25, 2019 - Use cautionMedical device
Hamilton Medical AG recalls HAMILTON-G5, with software versions less than or equal to 2.60 The HAMILTON-G5/S1 ventilators are designed for
Hamilton Medical recalls G5 ventilators with software versions 2.60 or older due to potential risk of unassisted breathing. Affected units have serial numbers 16192 and lower.
Hamilton MedicalMar 25, 2019 - Use cautionMedical device
Philips Medical Systems Nederlands recalls Ingenia Ambition S (781359), Ingenia Ambition X (781356) with Magnet Energization Device (MED), Philips MR systems are
Philips recalls Ingenia Ambition S and X MRI scanners with Magnet Energization Device (MED) due to potential electrical shocks during servicing. Affected units have specific serial numbers; contact Philips for details.
PhilipsMar 25, 2019 - Lower riskMedical device
Change Healthcare Israel Ltd. recalls McKesson Cardiology Hemo
McKesson Cardiology Hemo software version 13.x has medication data discrepancies between procedure screens and patient records. Affected healthcare providers should verify medication data accuracy to prevent errors.
McKesson Cardiology HemoMar 25, 2019 - Lower riskMedical device
Canon Medical System, USA, INC. recalls Canon Aquilion One, Model TSX-305A/3 V8.3 with FIRST 2.1
Canon recalls certain Aquilion One CT scanners (TSX-305A/3 V8.3 with FIRST 2.1) due to scanning interruptions and potential data loss if the system fails to shut down properly.
CanonMar 25, 2019 - Lower riskDrug
Glenmark Pharmaceuticals Inc., USA recalls Pravastatin Sodium Tablets USP, 20 mg, 500-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd. Plot
Glenmark Pharmaceuticals recalls 20mg Pravastatin tablets due to foreign tablets in some bottles. This may cause harm if taken. Check your bottle's NDC 68462-196-05 and lot number 17181491.
GlenmarkMar 25, 2019 - Lower riskDrug
Lohxa LLC recalls Bismuth Subsalicylate Oral Suspension 262mg/15mL, unit dose cups, OTC, Rpkg. By.: Lohxa Worcester, MA, NDC 70166-059-01
Lohxa recalls Bismuth Subsalicylate Oral Suspension 262mg/15mL unit dose cups due to incorrect expiration date on labels. Consumers should check labels for lot number M030042P and expiration date 01/2020.
LohxaMar 25, 2019 - Use cautionFood
Rice Valley recalls Rice Valley Ready Cooked Noodles and Instant Noodles, Net Wt, 14 oz. plastic bag - Perishable, Keep Refrigerate UPC 9
Rice Valley recalls 14 oz. Ready Cooked and Instant Noodles due to undeclared Yellow 5 & 6 dyes, posing allergy risks.
Rice ValleyMar 25, 2019 - Use cautionMeat & poultry
Tip Top Poultry, Inc. Recalls Fully Cooked, Diced Chicken Products due to Misbranding and Undeclared Allergens
USDA recalls 100 lbs of frozen diced chicken products from Tip Top Poultry due to undeclared soy allergen and misbranding as diced chicken instead of grilled strips.
Tip Top PoultryMar 23, 2019 - Use cautionMeat & poultry
North Country Smokehouse Recalls Ready-To-Eat Sausage Products due to Possible Foreign Matter Contamination
USDA FSIS recalls 2,686 pounds of ready-to-eat sausages from North Country Smokehouse that may contain metal fragments. Consumers are urged not to eat these products and should discard or return them.
North Country SmokehouseMar 23, 2019 - Lower riskMeat & poultry
Two Brothers Pork Skins Recalls Pork Skin Products Due to Misbranding and Failure to Produce Under A HACCP Plan
USDA FSIS recalls pork skin products from Two Brothers Pork Skins due to misbranding and failure to meet HACCP safety standards. Products were produced without proper safety controls and missing safe handling instructions.
Two Brothers Pork SkinsMar 22, 2019 - Use cautionVehicle
FORD TRANSIT CONNECT (2018) recall — Seats
Recall of 2018 Ford Transit Connects with Freedman seats due to potential seat cushion unlocking in crashes. Owners must contact Freedman for repair kit by December 19, 2019.
FORD TRANSIT CONNECTMar 22, 2019 - Use cautionVehicle
TIFFIN BUS (2019) recall — Electrical System
Tiffin recalls 2018-2019 Phaeton, Allegro Bus, and Zephyr motorhomes due to improperly secured electrical wires that may overheat and cause fire.
TiffinMar 22, 2019 - Use cautionVehicle
FORD F-550 (2019) recall — Exterior Lighting
Watts Manufacturing is recalling 2019 Ford F-550 vehicles with Whelen brake lights that may illuminate without pressing the brake pedal, potentially causing crashes. Owners should contact Watts Manufacturing for free replacement.
Watts ManufacturingMar 22, 2019 - Use cautionVehicle
FLEETWOOD FLAIR (2019) recall — Electrical System
REV is recalling 2019 Fleetwood Flair motorhomes due to a risk of fire from battery short circuits caused by metal battery straps contacting auxiliary battery terminals.
REVMar 22, 2019 - Use cautionVehicle
AUTOCAR XPEDITOR (2019) recall — Service Brakes
Autocar is recalling 2019-2020 Xpeditor vehicles with missing brake chamber clevis pin retainers that may increase stopping distance, risking crashes. Owners must contact Autocar for free brake repairs.
AutocarMar 22, 2019 - Use cautionMedical device
Microline Surgical, Inc. recalls TLS2 Thermal Ligating Shears, Catalog Number 132-131D
Microline Surgical recalls TLS2 Thermal Ligating Shears (Catalog 132-131D) due to high failure rates during surgery. Affected units may not function properly, risking procedure complications.
Microline SurgicalMar 22, 2019 - Use cautionMedical device
Stryker Communications recalls Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical lights are for usage in hospital treatment
Stryker recalls Berchtold Chromophare F628 surgical lights with serial numbers 83171-0017818 to 83171-0123938 due to risk of back cover detachment during use in hospitals.
Stryker CommunicationsMar 22, 2019 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Cios Alpha with software version VA30-mobile C-arm x-ray Material # 11105200 Product Usage: The Cios Alpha is a mobile
Siemens recalls Cios Alpha mobile X-ray systems with software version VA30-mobile due to potential premature failure of radiation components from continuous high-output use. Affected units may lose imaging capability.
SiemensMar 22, 2019 - Use cautionMedical device
Cardinal Health 200, LLC recalls ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and
Cardinal Health recalls ChemoPlus chemotherapy spill kits with natural rubber latex in safety goggles. This may cause allergic reactions. Affected kits have specific product codes and lot numbers listed.
Cardinal HealthMar 22, 2019 - UnratedDrug
Auro Pharmacies Inc. DBA Central Drugs recalls Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.
Central Drugs recalls Biotin 10 mg/mL injection vials due to failed pH specification. This may affect product safety and labeling accuracy.
Central DrugsMar 22, 2019 - Stop using nowDrug
InvaGen Pharmaceuticals, Inc. recalls Testosterone Cypionate Injection, USP, 1000 mg/10 mL (100 mg/mL), For intramuscular use only, 10 mL Vial,
InvaGen Pharmaceuticals recalls testosterone cypionate injections with particulate matter. Affected lots manufactured in India and shipped to US. Stop using immediately if you have the recalled product.
InvaGen PharmaceuticalsMar 22, 2019 - UnratedDrug
Lupin Pharmaceuticals Inc. recalls Fayosim (levonorgestrel and ethinyl estradiol) tablets USP, (0.15 mg/0.02 mg, 0.15 mg/0.025 mg, 0.15 mg/0.03 mg) and
Lupin Pharmaceuticals recalls Fayosim birth control tablets due to impurities detected in stability testing. These tablets may contain harmful substances that could cause serious health risks if used.
Lupin PharmaceuticalsMar 22, 2019 - Lower riskFood
Newport Ingredients recalls Maika'i Sweet Honey Nut Snack Mix, Honey Sesame Sticks, Almonds, Pumpkin Seeds, Peanuts, Pistachios & Pecans. NET WT. 8
Newport Ingredients recalls Maika'i Sweet Honey Nut Snack Mix and related products due to undeclared milk. This poses a risk for people with milk allergies. Consumers should check product labels and contact the manufacturer for details.
Newport IngredientsMar 22, 2019 - Stop using nowFood
Newly Weds Foods Inc recalls Commercial Breader Batter; B56666 BREADER X1; 50 pound bag
Newly Weds Foods recalls 2,800 lbs of Commercial Breader Batter (Lot CD032119B) due to potential plastic contamination. Check your inventory immediately.
Newly Weds FoodsMar 22, 2019 - Stop using nowMeat & poultry
Tyson Foods, Inc. Recalls Chicken Strip Products due to Possible Foreign Matter Contamination
Tyson Foods recalls ~69,093 lbs of frozen chicken strips due to possible metal contamination. Check your freezer for affected products and do not eat them.
Tyson FoodsMar 21, 2019 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls syngo.via syngo.CT Cardiac Function, Model Number 10496180 Product Usage: Syngo.CT Cardiac Planning and syngo CT.
Siemens recalls syngo.CT Cardiac Function software (model 10496180) due to potential wrong measurements during TAVI planning. Affected software versions VA20A, VA30A, VB10A may cause inaccurate annulus plane measurements.
SiemensMar 21, 2019 - Use cautionMedical device
Flowonix Medical Inc recalls Prometra Programmable Pump, Cat. No. 11827 For intrathecal infusion.
Flowonix recalls Prometra Programmable Pump (Cat. No. 11827) for intrathecal infusion due to unexpected shutdowns when Error 115 occurs, caused by software defects in specific programming scenarios.
FlowonixMar 21, 2019
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