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
35,006 found- Lower riskMedical device
Boston Scientific Corporation recalls Captivator Polypectomy Snare, Single-Use Polypectomy Snare consists of a flexible wire cable and loop which can be
Boston Scientific recalls certain Captivator Polypectomy Snare devices due to potential inability to cut and remove polyps, which could lead to prolonged procedures, tissue damage, or bleeding. Affected units have specific lot numbers and expiration dates.
Boston ScientificJul 6, 2020 - Use cautionMedical device
OrthoPediatrics Corp recalls Orthopedics 6.0MM ROD, COCR, SINGLE HEX, 500MM LENGTH-The RESPONSE" 5.5/6.0 Spine System is intended for immobilization
OrthoPediatrics recalls 6.0MM spine rods with incorrect laser etching that could lead to unintended fractures. Affected models include 00-1300-6053 (Lot 108332-A).
OrthoPediatricsJul 6, 2020 - Lower riskMedical device
Gentueri Inc recalls Gentueri Viral Transport Medium Kit with 8cm Breakpoint Swab
Gentueri Inc recalls Viral Transport Medium Kits with 8cm Breakpoint Swab due to sterility testing failures and contamination evidence. Affected kits may pose infection risks.
Gentuer: IncJul 6, 2020 - Use cautionMedical device
TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device
Teleflex Medical recalls Rusch Greenlite laryngoscopes with specific product codes due to potential breaking at welded joints during use, which could lead to injury during tracheal intubation procedures.
Teleflex MedicalJul 6, 2020 - Lower riskMedical device
ICU Medical, Inc. recalls APPX 0.75ml, 6-Port NanoClave Manifold (Glow, Red, Blue, Purple, Yellow Rings)BCV. 1 unit per pouch, 50 pouches per
ICU Medical recalls 50 pouches of 0.75ml 6-Port NanoClave Manifolds due to potential seal failure with spikes. Affected units may not seal properly, risking infection during medical fluid administration.
ICU MedicalJul 6, 2020 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Clonazepam Orally Disintegrating Tablets, USP, 0.125 mg, 60-count bottle, Rx only, Mfg by: Sun Pharmaceutical
Sun Pharmaceutical recalls 0.125 mg Clonazepam orally disintegrating tablets due to cross contamination with clozapine during stability testing. Affected lots may pose health risks.
Sun PharmaceuticalJul 6, 2020 - Lower riskDrug
Allergan PLC recalls Skin Medica Acne System, Contains: Purifying Foaming Wash (Salicylic Acid 2.0%), 5 fl oz.; Purifying Toner (Salicylic
Allergan recalls Skin Medica Acne System products that failed drug assay tests at 12 and 24 months, potentially containing insufficient salicylic acid and benzoyl peroxide.
AllerganJul 6, 2020 - Stop using nowFood
Lamb Weston Inc recalls WinCo Foods Tater Bites Shaped, Shredded Potatoes, frozen product. Retail 32 oz. poly bag has UPC 0 70552 30303 4. The
WinCo Foods recalls frozen Tater Bites due to potential foreign material contamination. Check your UPC and lot numbers for details.
WinCo FoodsJul 6, 2020 - Use cautionVehicle
CHEVROLET SS (2016) recall — Steering
GM recalls 2016 Chevrolet SS vehicles due to potential loss of power steering assist, increasing crash risk. Owners must have steering gear assembly replaced free by dealers.
ChevroletJul 5, 2020 - Use cautionVehicle
AUTOCAR XPEDITOR (2019) recall — Traction Control System
Autocar is recalling 2016-2020 Xpeditor vehicles with faulty traction control ECUs that may malfunction without warning, increasing crash risk. Owners must contact Autocar for free reprogramming.
AutocarJul 5, 2020 - Use cautionVehicle
INTERNATIONAL LT (2020) recall — Engine
Navistar recalls 2018-2020 International LT trucks due to potential engine connecting rod failure causing unexpected shutdowns and crash risks. Owners must contact Navistar for free repairs.
NavistarJul 5, 2020 - Lower riskMedical device
Dynex Technologies, Inc. recalls DYNEX Agility, Agility Analyzer, Model No. 67000
Dynex recalls Agility Analyzer Model 67000 software v1.4.3 due to risk of using incorrect control samples, which may delay patient results. Affected units have specific serial numbers.
DynexJul 5, 2020 - Use cautionDrug
Granules Pharmaceuticals Inc recalls Metformin Hydrochloride Extended-Release Tablets USP, 750 mg, a) 100 ct. bottle (NDC 70010-492-01) and 500 ct. bottle
Granules Pharmaceuticals recalls specific lots of Metformin Hydrochloride Extended-Release Tablets due to N-Nitrosodimethylamine (NDMA) impurity levels exceeding FDA limits.
Granules PharmaceuticalsJul 3, 2020 - Use cautionMedical device
Whirlpool Corporation recalls PAPR (Powered Air-Purifying Respirator) - Model# WLPAPR20W1
Whirlpool recalls PAPR model WLPAPR20W1 with potential loose headband causing face shield to slip. Affected units sold in 2020 week 20. Stop using immediately.
WhirlpoolJul 2, 2020 - Lower riskDrug
Edge Pharma, LLC recalls Vancomycin HCL 1.5 mg Edge Pharma, LLC 856 Hercules Dr. Colchester, VT 05446 NDC 05446-1458-01
Edge Pharma recalls Vancomycin HCL 1.5mg (NDC 05446-1458-01) due to labeling error on declared strength. Affected units may have incorrect dosage information.
Edge PharmaJul 2, 2020 - Stop using nowDrug
AAA Cosmetica, SA de CV recalls bio aaa Advance Hand Sanitizer Ethyl Alcohol 70%, Unscented, 16.23 Oz (480 mL), Distributed By: Payless Janitorial
AAA Cosmetica recalls unscented 70% ethyl alcohol hand sanitizer due to methanol contamination. This chemical can cause serious health risks if ingested or absorbed through skin. Consumers should stop using the product immediately.
AAA CosmeticaJul 2, 2020 - UnratedDrug
Lupin Pharmaceuticals Inc. recalls Cefdinir for Oral Suspension USP, 250 mg/5mL, packaged in 60 mL bottles, Rx only, Manufactured for: Lupin
Lupin Pharmaceuticals recalls Cefdinir oral suspension (250mg/5mL) due to potential superpotent drug levels. This prescription medication was manufactured in India and distributed in the US. Consumers should contact Lupin for details.
LupinJul 2, 2020 - Use cautionDrug
MasterPharm LLC recalls Formula 82M (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone acetonide 0.01%), a) 0.5 FL OZ (15 mL), b) 2 FL OZ (60 mL)
MasterPharm LLC recalls Formula 82M (Minoxidil/Tretinoin/Fluocinolone) bottles due to lack of processing controls. Check lot numbers and expiration dates.
MasterPharmJul 2, 2020 - Lower riskFood
Hostess Brands, LLC recalls Hostess Raspberry Zingers, Raspberry Iced Cake With Creamy Fillling, packaged in the following ways: 1) in boxes
Hostess recalls Raspberry Zingers and Iced Cake products with mold risk before best by date. Consumers should check UPCs and discard if mold present.
HostessJul 2, 2020 - Stop using nowConsumer product
Polaris Recalls Ranger and General Utility Vehicles Due to Crash Hazard (Recall Alert)
Polaris recalls 2019-2020 Ranger and General UTVs due to throttle failure after engine restarts, which can cause sudden acceleration and crashes. Owners must stop using and contact a dealer for repair.
PolarisJul 2, 2020 - Stop using nowConsumer product
Polaris Recalls Phoenix 200 All-Terrain Vehicles ATVs Due to Crash Hazard (Recall Alert)
Polaris recalls 2018-2020 Phoenix 200 ATVs due to potential throttle lever stop failure causing crashes. Owners must stop using and contact a dealer for free inspection or repair.
PolarisJul 2, 2020 - Use cautionConsumer product
Edens Garden Recalls Wintergreen and Birch Essential Oils Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Poisoning (Recall Alert)
Edens Garden recalls wintergreen and birch essential oils due to non-child-resistant packaging, risking poisoning if young children swallow. Consumers should store out of reach and get free replacements.
Edens GardenJul 2, 2020 - Stop using nowConsumer product
Avalon Furniture Recalls Cottage Town Bedroom Furniture Sold at Rooms To Go Due to Violation of Federal Lead Paint Ban; Risk of Poisoning (Recall Alert)
Avalon Furniture recalls Cottage Town Bedroom Furniture sold at Rooms To Go due to lead paint exceeding federal standards. Risk of poisoning for young children. Consumers must stop using and get free replacement.
Avalon FurnitureJul 2, 2020 - Stop using nowConsumer product
A Better You! Recalls Belecoo Strollers Due to Violation of Federal Stroller and Carriage Safety Standard; Fall, Entrapment and Strangulation Hazards (Recall Alert)
A Better You! recalls Belecoo 535-S baby strollers due to fall, entrapment and strangulation hazards from design flaws. Consumers must stop using and get refunds.
A Better You!Jul 2, 2020 - Use cautionMedical device
ICU Medical, Inc. recalls REF MC330209 6' (15 cm) Appx 0.09 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, 0.2 Micron Filter, 1.2 Micron
ICU Medical recalls specific IV sets with incorrect 0.2 micron filters that may cause infections during medical use. Affected units include model MC330209 with lot numbers 4447222, 4536285, 4572773, 4603405.
ICU MedicalJul 1, 2020 - UnratedDrug
Spartan Chemical Co Inc recalls Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1% - antimicrobial), For Institutional and Industrial Use Only,
Spartan Chemical recalls Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1%) for microbial contamination. Products sold for industrial use only.
Spartan ChemicalJul 1, 2020 - UnratedDrug
Preferred Pharmaceuticals, Inc. recalls Lidothol Patch, Lidocaine 4.5% & Menthol 5%, In each patch: lidocaine 4.5% topical anesthetic, menthol 5% topical
Preferred Pharmaceuticals recalls Lidothol Patches due to lost batch records. Check lot numbers H0218Z, H1518J, I2018L, J2918C, L1018Q, A0419M, G0519G.
LidotholJul 1, 2020 - Use cautionConsumer product
Boy Scouts of America Recalls Cub Scout Activity Pins Due to Violation of the Federal Lead Content Ban
Boy Scouts of America recalls Cub Scout activity pins due to lead content exceeding federal safety limits. These pins pose health risks if ingested by young children. Consumers should stop using and return items for refunds or credits.
Boy Scouts of AmericaJul 1, 2020 - Use cautionVehicle
VOLVO S60 (2018) recall — Seat Belts
Volvo recalls 2018 S60 models with seat belt anchor cable that may fatigue, increasing crash injury risk. Owners must have seat belt cable replaced by dealers.
VolvoJun 30, 2020 - Use cautionMedical device
Philips North America, LLC recalls IntelliVue MX800 patient monitor, model no. 865240
Philips recalls IntelliVue MX800 patient monitors with model 865240 due to defective power supplies that may energize metal parts or cause monitor failure if grounding instructions aren't followed.
PhilipsJun 30, 2020
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