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
35,004 found- Stop using nowConsumer product
Polaris Recalls Model Year 2018 to 2020 Ranger XP 1000 Off-Road Vehicles Due to Fire Hazard (Recall Alert)
Polaris recalls 2018-2020 Ranger XP 1000 and CREW XP 1000 off-road vehicles due to fire risk from clutch belt failure. Owners must stop using and get repairs.
PolarisApr 16, 2020 - Stop using nowConsumer product
MTD Southwest Recalls Trimmers and Polesaws Due to Laceration Hazard
MTD Southwest recalls Troy-Bilt and Craftsman trimmers and Remington polesaws with rotating heads that can cause lacerations when throttle is released. Consumers must stop using and get free replacements.
MTD SouthwestApr 16, 2020 - Use cautionConsumer product
Dr. Adorable Recalls Sweet Birch Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning; Sold Exclusively on Amazon.com (Recall Alert)
Dr. Adorable recalls sweet birch essential oil bottles due to non-child-resistant packaging, risking poisoning if young children swallow. Consumers should store out of reach and get refunds.
Dr. AdorableApr 16, 2020 - Lower riskMedical device
C.R. Bard Inc recalls SureStep Foley Tray System - Product Usage: Intended for use in the drainage and/or collection and/or measurement of
C.R. Bard recalls SureStep Foley Tray System due to potential white paper residue on catheters. Affected units have specific lot numbers and expiration dates. Consumers should contact for details.
C.R. BardApr 15, 2020 - Use cautionMedical device
Cook Inc. recalls Formula 418 Renal Balloon-Expandable Stent, RPN FOR418-18-80-6-12, Order Number (GPN) G56611 Balloon-expandable stent
Cook Inc. recalls Formula 418 Renal Balloon-Expandable Stents (lot 10153876) due to potential dislodgement during deployment, which may require additional intervention. Learn if your stent is affected and what to do.
Cook Inc.Apr 15, 2020 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Cefixime for Oral Suspension USP, 100mg/5mL, Rx Only, Manufactured for: Lupin Pharmaceutical, Inc. Baltimore, Maryland
Lupin Pharmaceuticals recalls Cefixime oral suspension (100mg/5mL) due to low potency from stability testing. Affected lots may not contain full active ingredient.
LupinApr 15, 2020 - UnratedDrug
H J Harkins Company Inc dba Pharma Pac recalls Acetaminophen and Codeine Phosphate 300/30 mg tablet, packaged in: a) 10-count bottle (NDC 52959-0003-10), b) 12-count
Pharma Pac recalls acetaminophen-codeine tablets due to cGMP deviations. Products sold in 10-60 count bottles with specific NDC numbers. No remedy provided in official notice.
Pharma PacApr 15, 2020 - Stop using nowDrug
Summitt Labs recalls KORE ORGANIC CBD Oil Watermelon 15mg*, 30 mL dropper bottles, Handcrafted By Summitt Labs, UPC 8 5765000812 8,
Summitt Labs recalls KORE ORGANIC CBD Oil Watermelon 15mg due to elevated lead levels. Check your lot and batch numbers for details.
KORE ORGANICApr 15, 2020 - Lower riskDrug
Amneal Pharmaceuticals of New York, LLC recalls Nizatidine Oral Solution, 15 mg/mL (75 mg/5mL) USP 480 mL bottles, Rx Only Distributed by: Gemini Laboratories, LLC
Amneal recalls Nizatidine Oral Solution bottles with potential N-Nitrosodimethylamine (NDMA) levels above FDA limits. This medication is prescription-only and distributed by Gemini Laboratories.
AmnealApr 15, 2020 - Lower riskFood
Dole Fresh Vegetables Inc recalls Hearts of Romaine. Product is fresh and packaged in 9 ounce (255g) plastic bags.
Dole recalls Hearts of Romaine lettuce due to potential low chlorine wash levels in some shipments. This may affect food safety. Check your product for the batch codes B104020 or B104021.
DoleApr 15, 2020 - Lower riskFood
Absorb Health LLC recalls Absorb Health Advanced Joint Relief Joint Health; 510mg; 90 CAPSULES; Manufactured for: Absorb Health, 106 Countryside
Absorb Health recalls 90-count joint relief capsules due to missing shellfish allergen label. This affects consumers with shellfish allergies.
Absorb HealthApr 15, 2020 - Use cautionVehicle
FREIGHTLINER BUSINESS CLASS M2 (2020) recall — Exterior Lighting
Daimler Trucks North America recalls certain 2020 Freightliner Business Class M2 trucks with rear reflective tape partially covered by mudflap hanger bracket, reducing rear visibility and crash risk. Free inspection and repositioning by dealers.
Daimler Trucks North AmericaApr 14, 2020 - Lower riskMedical device
Becton Dickinson & Co. recalls BD BBLTM Gram Crystal Violet 250mL-- IVD Primary stain for Staining Microorganisms, Catalog Number: 212525 - Product
Becton Dickinson recalls BD BBLTM Gram Crystal Violet 250mL IVD primary stain for false-positive Gram stains. Affected lots from 05/12/20 to 07/31/21 may cause misdiagnosis of bacteria.
Becton DickinsonApr 14, 2020 - Lower riskDrug
MasterPharm LLC recalls Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle, Compounded Product Not for Resale,
MasterPharm recalls 30-count and 90-count Finasteride Plus 1.25mg capsules that contain minoxidil due to cross contamination. This may cause unintended side effects. Consumers should contact the manufacturer for details.
MasterPharmApr 14, 2020 - UnratedDrug
B & B Pharmaceuticals, Inc. recalls Estradiol, USP (Non-Micronized) (Hemihydrate), packaged in: a) 500 grams (NDC 63275-9900-8), b) 100 grams (NDC
B & B Pharmaceuticals recalls estradiol products containing foreign Teflon material from specific lots. Consumers should contact the company for details on affected products and next steps.
B & B PharmaceuticalsApr 14, 2020 - Lower riskMedical device
Philips North America, LLC recalls Magnetic Resonance Imaging Diagnostic Device accessory - Product Usage: The chest pneumograph (also referred to as the
Philips recalls chest pneumographs made since 1996 due to missing natural rubber latex warning on labels. Healthcare users should check if their device contains latex.
PhilipsApr 13, 2020 - Lower riskMedical device
Ivoclar Vivadent AG recalls Ivoclar Vivadent IPS e.max ZirCAD CER/inLab Start.Kit LT - ceramic for dental use, intended for IPS e.max ZirCAD
Ivoclar Vivadent recalls IPS e.max ZirCAD CER/inLab Start.Kit LT ceramic for dental use due to restorations cracking during sintering. Affected units have specific product numbers and lot numbers.
Ivoclar VivadentApr 13, 2020 - Use cautionMedical device
K2M, Inc recalls K2M, ALEUTIAN Interbody Spacer Systems, EN AN Lordotic Spreader, Stainless Steel, Non-Sterile, Qty 1, Catalog #
K2M recalls Aleutian Anatomically Narrow Lordotic Spreader systems due to risk of spreader tip breaking during spinal procedures. Affected units include specific catalog numbers and lot numbers. Contact K2M for details.
K2MApr 13, 2020 - UnratedMedical device
American Contract Systems recalls Sterile Custom Packs to be used in surgical procedures.
American Contract Systems recalls sterile surgical gowns made in an unregistered FDA facility. These packs may not meet safety standards for surgical use. Affected kits include specific tray numbers and expiration dates.
American Contract SystemsApr 13, 2020 - Use cautionMedical device
Philips North America, LLC recalls Philips HeartStart XL Defibrillator/Monitor (Model number M4735A) - Product Usage: is for use in the hospital by
Philips recalls HeartStart XL Defibrillators (Model M4735A) for potential incorrect shock delivery due to a faulty therapy switch. All units are affected and have been discontinued.
PhilipsApr 13, 2020 - Use cautionVehicle
TOYOTA COROLLA (2020) recall — Fuel System, Gasoline
Toyota is recalling 2020 Corollas with a faulty fuel pump that can cause engine stalling while driving, increasing crash risk. Owners will receive free fuel pump replacements by late March 2021.
ToyotaApr 11, 2020 - Use cautionVehicle
BMW X5 (2020) recall — Suspension
BMW is recalling certain 2020 X5 models due to potential weld separation in front suspension, which could affect vehicle handling and increase crash risk. Owners should contact BMW for free replacement.
BMWApr 11, 2020 - Lower riskFood
DSD Merchandisers, Inc. recalls Roasted/Salted Deluxe Mixed Nuts; Net Wt. 10 oz./284 g, Clear plastic container UPC 65143370994 Cashews, Almonds,
DSD Merchandisers recalls 10oz mixed nuts for not listing peanuts in labeling. This affects products sold with UPC 65143370994. No action needed as peanuts are tree nuts.
DSD MerchandisersApr 11, 2020 - Stop using nowMeat & poultry
Conagra Brands, Inc. Recalls Frozen Not-Ready-to-Eat Chicken Bowl Products Due to Possible Foreign Matter Contamination
Conagra recalls frozen chicken bowl products from 2020 due to possible small rock contamination. Consumers are urged not to eat these items and should discard them immediately.
ConagraApr 10, 2020 - Lower riskMeat & poultry
Jowett Farms Corporation Recalls Pork Products Produced without Benefit of Import Inspection
USDA recalls 42,587 pounds of raw pork trimmings from Jowett Farms that were not inspected before import into the US. Consumers urged not to eat these products.
Jowett FarmsApr 10, 2020 - UnratedMedical device
Philips North America, LLC recalls HeartStart MRx Processor Board PCA Replacement Kits 453563478461, a component of the Philips HeartStart MRx
Philips recalls HeartStart MRx Processor Board PCA Replacement Kits with damaged ESD bags that could cause injury during medical device use. Affected units have specific serial numbers.
PhilipsApr 10, 2020 - Use cautionMedical device
Philips North America, LLC recalls Philips Zenition 70, System code 718133 - Product Usage: The devices are used for radiological guidance and
Philips recalls Zenition 70 systems with serial numbers starting 3537562050278101213476734193145863059512154. Cable strain may cause electrical exposure or video loss.
PhilipsApr 10, 2020 - Use cautionMedical device
Medtronic Inc. recalls Medtronic Implantable Insulin Pump System, REF: MMT-2007D, Sterile EO, CE 0459 UDI: 00763000043001
Medtronic recalls insulin pumps with specific serial numbers due to potential endotoxin levels that could cause fever, hypotension, or life-threatening reactions. Affected pumps were produced from May 21, 2019 onward.
MedtronicApr 10, 2020 - Lower riskFood
Champlain Chocolate Company recalls Lake Champlain CHOCOLATES, COIN DARK BULK ORG, NET WT 48 OZ (1.3 kg), APPROX 186 PIECES, INGREDIENTS: DARK CHOCOLATE
Champlain Chocolate Company recalls Lake Champlain CHOCOLATES due to undeclared milk content. Consumers should check product labels for the UPC 7 69933 02301 1.
Champlain Chocolate CompanyApr 10, 2020 - Lower riskFood
Whole Foods Market recalls Whole Foods Market Minestrone Soup PLU code printed on the product scale labels beginning with 248529 for soup sold in
Whole Foods Market recalls Minestrone Soup with PLU codes starting 248529 or 246691 sold before April 17, 2020. Product may contain undeclared milk.
Whole Foods MarketApr 10, 2020
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83,592 recalls tracked · 72,039 explained in plain English · 10,976 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.