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
34,893 found- Stop using nowConsumer product
Homestar North America Recalls Three-Drawer TV Chests Due to Serious Tip-Over and Entrapment Hazards; Sold Exclusively at Target.com (Recall Alert)
Homestar recalls three-drawer TV chests sold at Target due to serious tip-over and entrapment risks. Unanchored units can cause injuries or death to children. Consumers must stop using and secure units properly.
HomestarJun 28, 2017 - Use cautionVehicle
BUICK ENVISION (2017) recall — Equipment
GM recalls 2016-2017 Buick Envisions with improperly installed tablet holders that could cause head restraints to loosen in crashes. Owners must have head restraints inspected by dealers.
BuickJun 27, 2017 - Use cautionMedical device
Terumo Cardiovascular Systems Corporation recalls TERUMO(R) Overpressure Safety Valve, REF: (a) LH130 (b) LH130J
Terumo recalls overpressure safety valves (LH130/LH130J) with no flow reported. Affected units have specific lot codes and distribution dates. Stop using if no flow occurs.
TerumoJun 27, 2017 - Lower riskMedical device
Cardinal Health 200, LLC recalls Converters(R) Tiburon(R) Arthroscopy Drape, REF 9414, STERILE EO, Qty. 1, Cardinal Health, Waukegan, IL A surgical
Cardinal Health recalls some Tiburon Arthroscopy Drapes due to mismatched labels between product and packaging. Affected units have specific lot numbers and may not be sterile. Consumers should contact Cardinal Health for details.
Cardinal HealthJun 27, 2017 - Lower riskMedical device
NOVADAQ TECHNOLOGIES INC. recalls NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH2000 (single drape), Sterile, Rx. Manufactured for: Novadaq
Novadaq recalls sterile surgical drapes with potential pinholes that could breach sterile barriers during medical procedures. Affected units include specific model and lot numbers.
NovadaqJun 27, 2017 - Lower riskMedical device
Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables recalls Safety Deluxe Bone Marrow Biopsy/Aspiration Tray, Catalog # 986 Product Usage: Surgical procedure
Busse Hospital Disposables recalls Safety Deluxe Bone Marrow Biopsy/Aspiration Trays (Catalog #986) due to potential loose polypropylene foreign matter. Affected units include specific lot numbers with expiration dates.
Busse Hospital DisposablesJun 27, 2017 - Lower riskMedical device
Hologic, Inc recalls Tomcat Instrument, REF ASY-07379, Hologic Incorporated, automated laboratory sample processing instrument.
Hologic recalls Tomcat laboratory instruments with software anomaly that may cause incorrect patient results. Affected units include specific model numbers listed in the recall notice.
HologicJun 27, 2017 - Stop using nowFood
Primavera Nueva recalls Black Beans Bonanza Tamales with black beans. No Dairy:
Primavera Nueva recalls Black Beans Bonanza Tamales sold in CA. The product contains undeclared milk, posing a risk to those with dairy allergies.
Primavera NuevaJun 27, 2017 - Lower riskFood
Peanut Butter holdings, LLC recalls PB Crave, Coconut Milk Chocolate Peanut Butter Spread, NET WT 16 OZ (1 LB) -454 g. Plastic jars, 6 per case.
Peanut Butter holdings, LLC recalls PB Crave Coconut Milk Chocolate Peanut Butter Spread due to failure to list coconut as an allergen in labeling. This may cause allergic reactions for those with coconut allergies.
PB CraveJun 27, 2017 - Stop using nowConsumer product
Fireworks Recalled By American Promotional Events Due to Burn and Injury Hazards
TNT Red, White & Blue Smoke fireworks recalled due to risk of unexpected explosions after lighting, causing burn and injury hazards. Consumers must stop using and get a refund.
TNTJun 27, 2017 - Use cautionVehicle
FORD ESCAPE (2016) recall — Air Bags
Ford is recalling 2016 Escape vehicles with driver knee airbags that may not inflate properly during crashes, risking injury. Owners must have the airbag replaced free by August 8, 2017.
FordJun 26, 2017 - Use cautionVehicle
FREIGHTLINER BUSINESS CLASS M2 (2017) recall — Service Brakes, Air
Daimler Trucks North America recalls 2015-2017 Freightliner M2 Business Class trucks with potential air pressure loss in brakes, risking sudden parking brake activation and crashes.
Daimler Trucks North AmericaJun 26, 2017 - Use cautionVehicle
FORD TRANSIT (2017) recall — Power Train
Ford is recalling 2017 Transit vehicles with a faulty flexible coupling that may cause the vehicle to stop moving and roll if not properly secured, increasing crash risk. Owners must have the coupling replaced by dealers.
FordJun 26, 2017 - Use cautionVehicle
AUDI Q3 (2017) recall — Exterior Lighting
Volkswagen recalls certain 2016-2017 Audi Q3 vehicles where brake lights may not activate during emergency braking, increasing crash risk. Owners must contact Audi for free software update.
AudiJun 26, 2017 - Lower riskMedical device
Ameditech Inc recalls Alere iScreen Dx Urine Drug Screen Card, 20 Drug Detection, Kit Contents include 26 individually pouched devices and 1
Ameditech recalls Alere iScreen Dx Urine Drug Screen Cards due to incorrect labeling of PCP instead of TCA in the kit. This may cause misidentification of drugs in urine tests.
AmeditechJun 26, 2017 - Lower riskMedical device
Implant Direct Sybron Manufacturing, LLC recalls Spectra-System/Legacy Guided Surgery Handle Kit, Device Listing Number D245883. The Guided Handle Kit (G-HK) allows
Spectra-System recalls Legacy Guided Surgery Handle Kit (Device Listing D245883) due to small drill guide inserts potentially not fitting drills correctly. Affected units include Lot 65249, Sequence Number HE G-HKRev01.
Spectra-SystemJun 26, 2017 - Stop using nowMedical device
Certified Safety Mfg Inc recalls Burn Sheet, sterile - 60" x 96". Included in First Aid Kits: 36M - Delmarva Power/ACE - w/Logo, Certified Safety
Certified Safety recalls sterile burn sheets (60" x 96") that may shred, causing injury. Affected items include specific first aid kits. Stop using immediately.
Certified SafetyJun 26, 2017 - Lower riskMedical device
Encore Medical, Lp recalls Cobalt HV with Gentamicin, Cobalt Bone Cement 40GM, REF 402283, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS
Encore Medical recalls Cobalt HV with Gentamicin bone cement (REF 402283) due to potential packaging seal loss. This could compromise sterility during medical procedures. Affected patients should contact their doctor for guidance.
Encore MedicalJun 26, 2017 - Lower riskMedical device
Stryker Neurovascular recalls Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN
Stryker Neurovascular recalls some Stroke Fast Packs due to mismatched carton sleeve labels and physical contents. Affected units include specific lot numbers and model codes. Consumers should check their packaging for the listed identifiers.
Stryker NeurovascularJun 26, 2017 - Lower riskMedical device
Beckman Coulter Inc. recalls Coulter HmX CP and Coulter HmX AL Analyzers The purpose of the HmX Hematology Analyzer is to separate the normal
Beckman Coulter recalls HmX CP and HmX AL Analyzers that may fail to detect blasts in some blood samples, requiring additional testing for certain diagnoses.
Beckman CoulterJun 26, 2017 - UnratedDrug
VistaPharm, Inc. recalls Lactulose Solution, USP, 10 g/15 mL, dose cups delivers 15 mL packaged in 50-unit dose cups per case, Manufactured by
VistaPharm recalls Lactulose Solution due to microbial contamination. Product failed yeast/mold count tests. Affected units have specific NDC and lot numbers. No remedy stated in recall notice.
VistaPharmJun 26, 2017 - UnratedDrug
PharMedium Services, Llc recalls Succinylcholine Chloride Injection (Preserved) 20 mg per mL, 200 mg per 10 mL, 10 mL Total Volume in BD Syringe, For IV
PharMedium Services recalls specific lots of IV succinylcholine chloride injection due to lack of sterility assurance from manufacturing media fill failure.
PharMedium ServicesJun 26, 2017 - Lower riskFood
NatureBox, Inc. recalls NatureBox Mini Crispy Snickerdoodles: Cinnamon-sugar cookies made with whole wheat. Contains: Wheat, Milk and Egg.
NatureBox recalls Mini Crispy Snickerdoodles due to a cashew found in one product. This snack contains wheat, milk, and egg. Check lot numbers for affected items.
NatureBoxJun 26, 2017 - Lower riskFood
Shatto Milk Co recalls Cookin' Unsalted Butter, packaged in 8 oz plastic tubs. Plant # 29-685 Osborn, MO.
Shatto Milk Co recalls Cookin' Unsalt: Butter tubs from Osborn, MO with undeclared milk and wheat allergens. Consumers should check best by dates before November 2017.
Shatto Milk CoJun 26, 2017 - Stop using nowMeat & poultry
Overhill Farms, Inc. Recalls Chicken Products Due To Possible Foreign Matter Contamination
Overhill Farms recalls chicken bites products from 2016-2018 that may contain bone. Consumers are urged not to eat these items and should discard or return them.
Overhill FarmsJun 24, 2017 - Stop using nowMeat & poultry
Maxi Canada, Inc. Recalls Breaded Chicken Products Due to Misbranding and Undeclared Allergens
Maxi Canada recalls over 4 million lbs of Yummy breaded chicken products due to undeclared milk. Check your freezer for affected lots and barcodes.
YummyJun 24, 2017 - Lower riskMeat & poultry
The Wornick Company Recalls Beef Ravioli Products Due To Misbranding and Undeclared Allergens
USDA recalls 61,538 pounds of Wornick beef ravioli products due to undeclared milk allergen. Consumers urged not to consume; products should be thrown away or returned.
WornickJun 23, 2017 - Use cautionVehicle
HONDA ODYSSEY (2018) recall — Seat Belts
Honda recalls 2018 Odyssey vehicles with third row seat belt that may not latch securely during crashes, risking occupant injury. Owners must have seat belt inspected and replaced if needed.
HondaJun 23, 2017 - Lower riskMedical device
Xintec Corp recalls OptiLITE(TM) Products for Laser Surgery, Catalog Numbers: HTM1020F, HTM1040F, HTM1060F, HTM1010F; Manufactured by
Xintec Corp recalls OptiLITE laser surgery products (catalog numbers HTM1020F, HTM1040F, HTM1060F, HTM1010F) due to potential insufficient reprocessing instructions for cleaning and sterilization, which may not meet new standards.
Xintec CorpJun 23, 2017 - Use cautionMedical device
Exactech, Inc. recalls Truliant Tibial Trial Handle. To assist the surgeon in the implantation of Truliant Knee system components according to
Exactech recalls Trul:iant Tibial Trial Handle (Catalog 02-029-29-1000) due to risk of pin disassociation during surgery. Affected surgeons should contact Exactech for details.
ExactechJun 23, 2017
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