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
35,021 found- Stop using nowFood
Tim Campbell Farm LLC recalls Tim Campbell Farm flat parsley in wooden crate. Neither Net weight nor quantity stated on label; product is 30 count.
Tim Campbell Farm recalls flat parsley in wooden crates due to Listeria monocytogenes contamination. Product sold without net weight or quantity on label, 30-count items. Consumers should avoid use.
Tim Campbell FarmSep 2, 2020 - Use cautionConsumer product
IMMI Recalls Harnesses Made for Polaris, Can-Am, and Kawasaki UTVs Due to Injury Hazard
IMMI recalls SubZero and Click6 harnesses for Polaris, Can-Am, and Kawasaki UTVs due to missing stitching that could cause injury in crashes. Affected units include 2015-2020 models with specific part numbers.
IMMISep 2, 2020 - Use cautionConsumer product
Hanamint Recalls Swivel Rockers, Club Swivel Rockers and Club Swivel Gliders Due to Fall Hazard
Hanamint recalls swivel rockers and gliders due to risk of fall from chair post separating from base. Consumers must stop using and contact for free repair.
HanamintSep 2, 2020 - Stop using nowConsumer product
Advantus Recalls Fluorescent Computer Task Lamps Due to Burn Hazard
Advantus recalls LEDU Black Fluorescent Computer Task Lamps (Model L283MB) due to a burn hazard. Unplug immediately and contact Advantus for a full refund.
LEDUSep 2, 2020 - Stop using nowVehicle
NISSAN VERSA (2011) recall — Air Bags
Nissan is recalling 2011 Versa models with non-desiccated passenger air bag inflators that may explode due to propellant degradation, risking serious injury or death. Owners must have inflators replaced free of charge.
NissanSep 1, 2020 - Use cautionVehicle
FERRARI 458 ITALIA (2011) recall — Air Bags
Ferrari recalls 2011 458 Italia vehicles with potentially explosive air bag inflators. Replace with safer model to prevent serious injury or death.
FerrariSep 1, 2020 - Use cautionMedical device
Medline Industries Inc recalls ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended
Medline recalls ClearPro Closed Suction Catheter Model DYNCPDS14T due to reports of it breaking during use, which could cause injury. Affected units were sold in specific lots.
MedlineSep 1, 2020 - Use cautionMedical device
Fresenius Medical Care Holdings, Inc. recalls AquaBplus and AquaBplus B2 Water Purification System. For use with a hemodialysis system to remove organic and
Fresenius recalls AquaBplus and AquaBplus B2 water purification systems for hemodialysis use due to electrical safety risks from loose crimp connections that could cause shock to staff.
FreseniusSep 1, 2020 - Stop using nowDrug
The Protein Shoppe recalls Red-E Tablet, Proprietary Blend 3000 mg**, packaged in 1-count plastic bag stapled with cardboard labeling.
The Protein Shoppe recalls Red-E Tablets containing unapproved sildenafil, posing safety risks due to lack of FDA approval. Consumers should stop using these products immediately.
The Protein ShoppeSep 1, 2020 - Stop using nowMeat & poultry
Ukrop's Homestyle Foods Recalls Chicken Salad Product Due to Misbranding and an Undeclared Allergen
Ukrop's Homestyle Foods recalls ~1,202 lbs of chicken salad due to undeclared almonds. Check your fridge and do not consume.
Ukrop'sAug 31, 2020 - Lower riskMedical device
Cook Inc. recalls Pediatric Nephrostomy Stent Set, Reference Part Numbers 080208-S6 and 080208-S7, Order Numbers G15034 and G15035. The
Cook recalls pediatric nephrostomy stent sets with reference part numbers 080208-S6/S7 and order numbers G15034/G15035 due to reduced indwell time from 4 months to 4 weeks. The current instructions for use are being updated.
CookAug 31, 2020 - Lower riskMedical device
Ultradent Products, Inc. recalls PermaFlo Flowable Composite REF-UP 948 Shade: A2 - Product Usage: is a light cured, radiopaque, methacrylate based,
Ultradent recalls PermaFlo Flowable Composite REF-UP 948 Shade A2 due to potential cross contamination causing non-homogeneous material. Affected units have specific lot numbers and UPC codes.
Ultrad: a dental brandAug 31, 2020 - UnratedMedical device
Olympus Corporation of the Americas recalls Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to be used with an Olympus TV camera system, light
Olympus recalls CHF-CB30S choledoscope due to potential metal breakage and rubber displacement during surgery. Affected units lack 510(k) clearance and may cause injury.
OlympusAug 31, 2020 - Stop using nowMedical device
Roche Diagnostics Operations, Inc. recalls DISCOVERY ULTRA Advanced Staining System (RUO-Research Use Only) Material Number: 05987750001
Roche recalls all Discovery Ultra Advanced Staining Systems (RUO) due to potential fluid leaks causing electrical shorts, heat, smoke, and fire. No remedy specified in official notice.
RocheAug 31, 2020 - Lower riskMedical device
Vascular Solutions, Inc. recalls Langston Dual Lumen Catheter.
Vascular Solutions recalls Langston Dual Lumen Catheters with specific model numbers due to risk of inner lumen separating from hub during pressure injection. Affected units include lots 643376 to 673021.
Vascular SolutionsAug 31, 2020 - Lower riskMedical device
Olympus Corporation of the Americas recalls Olympus Medical Systems Corporation (OMSC) Evis Exera II Bronchovideoscope Olympus BF Type Q180 (BF-Q180) All serial
Olympus recalls all Evis Exera II Bronchovideoscopes (BF-Q180) due to higher patient infection rates compared to other OMSC models. No 510(k) clearance was issued for this device.
OlympusAug 31, 2020 - Lower riskMedical device
Encore Medical, LP recalls AltiVate Reverse Small Socket Insert, 44mm Semi Constrained - E-Plus, Part Number: 509-03-044 - Product Usage: Per IFU,
Encore Medical recalls AltiVate Reverse Small Socket Insert (Part 509-03-044) due to mislabeling that may delay or stop surgery. Affected units sold with lot number 964W100:1000.
Encore MedicalAug 31, 2020 - Lower riskMedical device
Biomet 3i, LLC recalls BELLATEK TITANIUM ABUTMENT 4.1MM Reference Number: EDAT4
Biomet recalls Bellatek Titanium Abutment 4.1mm (EDAT4) due to manufacturing misalignment risk. This may cause improper placement during dental procedures.
BiometAug 31, 2020 - Lower riskMedical device
Brainlab AG recalls Ultrasound Navigation Software 1.0 and Ultrasound Integration Software for Cranial/ENT Navigation 3.0.x and 3.1.x -
Brainlab recalls ultrasound navigation software versions 1.0 and 3.0.x/3.1.x due to inability to modify probe image width. This may affect surgical precision during minimally invasive procedures. Affected units include specific model numbers and subscription packages.
BrainlabAug 31, 2020 - Use cautionMedical device
ICU Medical, Inc. recalls 30" (76 cm) Appx 3.3 ml, 20 Drop Admin Set w/Integrated ChemoLock Drip Chamber, Spiros w/Red Cap, Hanger, REF: CL3011;
ICU Medical recalls specific IV sets with potential spinning luer leaks causing fluid contamination, exposure to hazardous medications, or blood loss. Affected models include CL3011 and others listed in the recall notice.
ICU MedicalAug 31, 2020 - Lower riskFood
Fresco Foods recalls Ancient Grain Jackfruit Bowl with Chickpeas & Edamame in a Thai Coconut Sauce, Eat Fresco, Keep Refrigerated, NET WT
Fresco Foods recalls Ancient Grain Jackfruit Bowl with Chickpeas & Edamame in Thai Coconut Sauce due to undisclosed anchovies. Check packaging for best by date (09/15/2020 or earlier).
Fresco FoodsAug 31, 2020 - Use cautionVehicle
PJ TRAILERS DE (2021) recall — Equipment
PJ Trailers is recalling certain 2020-2021 DE trailers due to potential dump box drop after attachment bolts fail, risking injury. Owners should contact customer service for free replacement of hydraulic units and bolts.
PJ TrailersAug 28, 2020 - Use cautionVehicle
HEARTLAND CYCLONE (2020) recall — Equipment
Heartland is recalling 2020 Cyclone trailers due to front landing legs that may buckle while parked, risking property damage or injury. Owners must contact Heartland for free repairs.
HeartlandAug 28, 2020 - Stop using nowVehicle
GRAND DESIGN SOLITUDE (2020) recall — Equipment
Grand Design is recalling 2017-2021 Solitude RVs due to LP gas leaks near refrigerator burners that could cause fire. Owners must have lines inspected and repaired free.
Grand DesignAug 28, 2020 - Lower riskMedical device
Smiths Medical ASD Inc. recalls Bivona Mid-Range Aire-Cuf Adult Tracheostomy Tube This tube is intended to provide direct airway access for a
Smiths Medical recalls Bivona Mid-Range Aire-Cuf Adult Tracheostomy Tubes due to incorrect size labeling on the label, which could lead to improper fitting.
Smiths MedicalAug 28, 2020 - Lower riskMedical device
Greiner Bio-One North America, Inc. recalls VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator, Item Number: 456018P - Product Usage: are used to collect,
Greiner Bio-One recalls 5mL CAT serum separator blood collection tubes with clotting problems. Affected lots may cause inaccurate blood test results. Contact for replacement.
Greiner Bio-OneAug 28, 2020 - Lower riskMedical device
Siemens Healthcare Diagnostics Inc recalls Siemens epoc BGEM Test Card-In vitro diagnostic device for the quantitative testing of samples of heparinized or
Siemens recalls specific lot of epoc BGEM Test Card for inconsistent glucose results, potentially delaying hyperglycemia diagnosis or causing unnecessary hypoglycemia treatment.
Siemens HealthcareAug 28, 2020 - Stop using nowFood
Hometown Food Company recalls Arrowhead Mills Organic Yellow Popcorn, 28oz bag, UPC: 0 7433347665 8, 6 retail bags per wholesale case, case item code
Hometown Food Company recalls Arrowhead Mills Organic Yellow Popcorn due to potential glass contamination. Check your UPC and lot numbers.
Arrowhead MillsAug 28, 2020 - Use cautionFood
Preferred Popcorn recalls Organic Yellow Popcorn packaged in the following ways: 1) Great Northern Organic Popcorn, Net Wt. 5 Pounds (2.26
Preferred Popcorn recalls organic yellow popcorn products that may contain tempered glass pieces between 3-7mm in size. Consumers should check UPCs and packaging details to identify affected items.
Preferred PopcornAug 28, 2020 - Stop using nowFood
EAGLE FAMILY FOODS GROUP LLC recalls 365 Whole Foods Market Organic Reduced fat &Sodium Popcorn, 6 oz. bag, UPC 099482435349, 10 retail units per wholesale
Eagle Family Foods recalls specific lots of 365 Whole Foods Market organic popcorn due to potential glass contamination. Check your UPC and best-by dates.
365 Whole Foods MarketAug 28, 2020
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