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
34,894 found- Lower riskMedical device
Phadia US Inc recalls ImmunoCAP Allergen c5, Ampicilloyl (article number 14-4450-01). ImmunoCAP Specific IgE is an in vitro quantitative
Phadia recalls ImmunoCAP Allergen c5 Ampicilloyl (article 14-4450-01) due to stability problems. This affects specific IgE test kits with lot numbers 990DS through 990DY.
PhadiaDec 18, 2017 - Lower riskMedical device
Johnson & Johnson Consumer, Inc. recalls COACH¿ Self-Adhering Sports Wrap (size: 2in)
Johnson & Johnson recalls select COACH Self-Adhering Sports Wraps due to potential natural latex allergy from early manufacturing. Affected products may cause allergic reactions in sensitive individuals.
COACHDec 18, 2017 - UnratedDrug
Osmotica Pharmaceutical Corp recalls Methylphenidate Hydrochloride Extended-release Tablets, USP 27 mg, 100-count bottles, Rx Only, Trigen Laboratories,
Osmotica Pharmaceutical Corp recalls 27mg methylphenidate tablets due to subpotent drug levels. Affected products have NDC 13811-707-10 and lot 170027A. No remedy specified in recall notice.
Osmot: Trigen LaboratoriesDec 18, 2017 - Stop using nowFood
Meijer Distribution, Inc recalls Meijer Michigan Harvest Salad 10 Oz retail unit in plastic container UPC: 7-08820-68400-3 4 retail containers per
Meijer recalls 10 oz Michigan Harvest Salad containers with potential Listeria monocytogenes contamination. Consumers should check UPC 7-08820-68400-3 and discard if purchased between Dec 17-21, 2017.
MeijerDec 18, 2017 - Lower riskFood
Barlean's Fishery Inc. recalls REEF NET brand Wild Pacific Smoked Salmon. Product is Ready-To-Eat, hot smoked, vacuum packaged in 1 lb.; 1.5 lbs.; and
Barlean's recalls REEF NET Wild Pacific Smoked Salmon due to undeclared soy lecithin. The product may contain soy lecithin without labeling, posing an allergen risk for those with soy allergies.
Barlean'sDec 18, 2017 - Lower riskFood
Gel Spice Co, Inc. recalls Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) and NET WT. 3-1/2 OZ (98 g) 25 Count
Gel Spice recalls beef bouillon cubes containing undeclared soy and wheat allergens. Consumers should check product dates and stop using if they have allergies.
Gel SpiceDec 18, 2017 - Lower riskFood
Ingles Markets recalls Frozen Buttermilk Biscuits 25 oz. bag (12 count) and 44 oz. bag (20 count)
Ingles Markets is recalling frozen buttermilk biscuits due to Listeria monocytogenes contamination detected in samples. Consumers should check product UPCs and discard affected items.
Ingles MarketsDec 18, 2017 - Stop using nowFood
Jack Brown Produce, Inc. recalls Gala, whole fresh apples; Metric Tray sizes, 50ct, 55ct, 60ct, 78ct, 113ct, 2# Poly bags, 3# Poly bags and 5# Mesh
Jack Brown Produce recalls Gala apples from specific lot numbers due to potential Listeria monocytogenes contamination. Consumers should avoid these products to prevent foodborne illness.
Jack Brown ProduceDec 17, 2017 - Stop using nowMeat & poultry
Piller's Fine Foods Recalls Ready-To-Eat Salami and Speck Products due to Possible Salmonella Adulteration
Piller's Fine Foods recalls ready-to-eat salami and speck products due to possible Salmonella contamination. Check your fridge for affected items.
Piller's Fine FoodsDec 16, 2017 - Use cautionVehicle
FREIGHTLINER CORONADO (2017) recall — Equipment
Daimler Trucks North America recalls 2017 Freightliner Coronado trucks with potentially defective fire extinguishers that may not function properly during fires, increasing injury risk. Owners must contact Kidde for a free replacement.
Daimler Trucks North AmericaDec 15, 2017 - Use cautionVehicle
NEWMAR MOUNTAIN AIRE (2018) recall — Equipment
Newmar is recalling 2018 motorhomes with potentially defective Kidde fire extinguishers that may not function properly in a fire, increasing injury risk. Owners must contact Kidde for a free replacement.
NewmarDec 15, 2017 - Use cautionVehicle
FOREST RIVER SANDPIPER (2018) recall — Equipment
Forest River is recalling 2018 Sandpiper trailers due to incorrect tire pressure placard causing premature wear and crash risk. Owners must get corrected placard installed free.
Forest RiverDec 15, 2017 - Use cautionVehicle
DUCATI MONSTER 1200 (2018) recall — Service Brakes, Hydraulic
Ducati is recalling certain 2015-2018 Monster 1200 motorcycles due to potential front brake master cylinder failure that could increase crash risk. Owners must contact Ducati for free replacement by February 15, 2018.
DucatiDec 15, 2017 - Use cautionMedical device
Arrow International Inc recalls ARROW ENDURANCE" Extended Dwell Peripheral Catheter System, Catalog Numbers: EDC-00820 & EDC-00820-B
Arrow recalls specific catheter systems with missing safety latches that could cause sharps injuries. Affected units have catalog numbers EDC-00820 or EDC-00820-B with listed lots. Contact Arrow for details.
ArrowDec 15, 2017 - Lower riskMedical device
Ameditech Inc recalls Alere iScreen Dx Urine Drug Screen Card
Ameditech recalls Alere iScreen Dx Urine Drug Screen Cards due to incorrect labeling of drug analytes. This could lead to misidentification of Tricyclic Antidepressants as Phencyclidine (PCP) in test results.
AmeditechDec 15, 2017 - Lower riskMedical device
Quidel Corporation recalls Sofia 2 Analyzer Catalog Number 20299 Sofia 2 is a bench top analyzer intended to be used with Cassette-based
Quidel recalls Sofia 2 Analyzer (Catalog 20299) with serial numbers listed. The device may have calibration errors that cause test failures, especially near assay cutoffs.
QuidelDec 15, 2017 - Use cautionMedical device
Philips Medical Systems (Cleveland) Inc recalls BrightView Model 882480 Product Usage: BrightView and BrightView X are gamma cameras designed for single or dual
Philips recalls BrightView Model 882480 gamma cameras due to risk of collimator dropping during exchange, potentially causing injury. Affected units have specific serial numbers listed in the recall notice.
Philips Medical SystemsDec 15, 2017 - Lower riskMedical device
DePuy Spine, Inc. recalls Confidence Plus Kit Spinal Cement System, Product Codes: 283910000 (GTIN: (01)10705034209623) and 283910000 (GTIN:
DePuy Spine recalls Confidence Plus Spinal Cement kits with certain lot numbers due to potential incorrect contrast medium levels, making them difficult to see on x-rays during medical procedures.
DePuy SpineDec 15, 2017 - Use cautionMedical device
Trumpf Medical Systems, Inc. recalls Camera System, Television, Surgical without audio Intended for transmission and documentation of surgical interventions
Trumpf Medical recalls surgical camera systems with serial numbers listed that emit excessive radiation, potentially causing hospital equipment to malfunction during surgery. Affected units must be checked by a professional.
Trumpf MedicalDec 15, 2017 - Lower riskMedical device
GE Healthcare, LLC recalls Uterine Electromyographic Monitor -Monica IF24 Interface System Product Usage: The Monica IF24 CTG Interface Device is
GE Healthcare recalls Monica IF24 Interface System units (model 105-PT-001) sold 2011-2016. If cables are removed and reconnected incorrectly, fetal and maternal heart rate signals may be swapped, potentially causing misdiagnosis during pregnancy monitoring.
GE HealthcareDec 15, 2017 - Stop using nowDrug
Amneal Pharmaceuticals recalls Fosphenytoin Sodium Injection, USP 500 mg PE*/10 mL, Made in India. Distributed by: Amneal Biosciences, Bridgewater, NJ
Amneal Pharmaceuticals recalls Fosphenytoin Sodium Injection (500 mg/10 mL) made in India due to particulate matter. Affected lots and expiration dates listed. Contact for remedy.
AmnealDec 15, 2017 - UnratedDrug
Akorn Inc recalls Gabapentin Oral Solution, 250 mg/5 mL (50 mg/mL) in a 470 mL amber-colored bottle, Rx Only. Manufactured by: Hi-Tech
Akorn recalls 470mL amber Gabapentin Oral Solution (Rx only) due to unapproved active ingredient in manufacturing. Consumers should contact Akorn for details.
AkornDec 15, 2017 - Lower riskDrug
B. Braun Medical Inc recalls 0.25% Acetic Acid Irrigation USP, 500 mL Plastic Irrigation Container (PIC), B. Braun Medical Inc. Irvine CA 92614-5895
B. Braun Medical recalls 500mL plastic irrigation containers with polyethylene particulate matter that could cause blockages or infections during medical use.
B. Braun MedicalDec 15, 2017 - Use cautionVehicle
FREIGHTLINER SPRINTER 3500 (2017) recall — Lane Departure
Daimler Vans USA recalls 2017 Sprinter 3500 vans. The Crosswind Assist system may fail to activate braking in strong winds, increasing crash risk.
Freightliner / Mercedes-BenzDec 14, 2017 - Use cautionVehicle
FLEETWOOD PACE ARROW (2018) recall — Equipment
REV is recalling 2018 Fleetwood Pace Arrow motorhomes due to satellite dish detaching while driving, increasing crash risk. Owners must have dish resecured by dealers free of charge.
REVDec 14, 2017 - Lower riskMedical device
Abbott Gmbh & Co. KG recalls ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent microparticle immunoassay (CMIA) for the quantitative
Abbott recalls ARCHITECT DHEA-S reagent kits that may produce falsely elevated DHEA-S test results when used on infants up to 60 days old. Affected lots have specific expiration dates and unique identifiers.
AbbottDec 14, 2017 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Dimension Lipase Flex¿ Reagent Cartridge - ( Lipase-esterase, enzymatic, photometric, lipase)
Siemens Healthcare recalls Dimension Lipase Flex Reagent Cartridge lot FB8109 due to calibration failure causing positive bias in test results. Affected units may produce inaccurate test results.
Siemens HealthcareDec 14, 2017 - Use cautionMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls 2008 K2 Hemodialysis Machine with software version 5.40, Models: (1) Hemodialysis SYS OLC/Diasafe PLS 190610, UDI
Recall of 2008 K2 Hemodialysis Machines with software version 5.40 due to potential high ultrafiltration rates during SLED dialysis programs.
Fresenius Medical CareDec 14, 2017 - Use cautionMedical device
Merit Medical Systems, Inc. recalls PreludeSNAP Splittable Hydrophilic and non-Hydrophilic Sheath Introducers, Catalog Numbers - PLS-1007, PLS-1008,
Merit Medical recalls specific PreludeSNAP Splittable Sheath Introducers due to intermittent splittable hub failure. Affected models include PLS-1007 to PLSX-1009.5 with certain lot numbers. Consumers should contact Merit Medical for details.
Merit MedicalDec 14, 2017 - Lower riskMedical device
Safe N Simple, LLC recalls DermaPro Waterproof Silicone Tape, SNS57232
Safe N Simple recalls DermaPro Waterproof Silicone Tape SNS57232 due to poor adhesion and difficulty peeling off the roll. Affected units sold from 20170716.
Safe N SimpleDec 14, 2017
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83,390 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.