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- Use cautionVehicle
HONDA CBR1000RR (2017) recall — Fuel System, Gasoline
Honda recalls 2017 CBR1000RR motorcycles with potential water in fuel tank causing engine stalling and crash risk. Free repairs available by December 22, 2017.
HondaOct 26, 2017 - Use cautionVehicle
JAGUAR XE (2018) recall — Electrical System
Jaguar is recalling 2018 XE vehicles with a potential instrument cluster that may go blank, risking loss of speed information and crash risk. Owners will receive software updates to fix the issue.
JaguarOct 26, 2017 - Use cautionVehicle
FOREST RIVER FLAGSTAFF (2018) recall — Equipment
Forest River recalls 2017-2018 Flagstaff travel trailers due to slide room arm potentially damaging rear tires, risking loss of vehicle control. Owners should contact customer service for free lift kit installation.
Forest RiverOct 26, 2017 - Lower riskMedical device
ConvaTec, Inc recalls SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible Collar, 10 pack, 45 mm, REF 411802. Intended
ConvaTec recalls 10-pack SUR-FIT Natura Moldable Durahesive Skin Barrier (REF 411802) due to incorrect labeling with a different product. Affected units were shipped in Lot 7H02242.
ConvaTecOct 26, 2017 - Lower riskMedical device
Arrow International Inc recalls Radial Artery Catheterization Kit; Model: AK-04220
Arrow recalls Radial Artery Catheterization Kit model AK-04220 with povidone iodine prep pads that expire after 24 months instead of 36. Affected kits have specific lot numbers and expiration dates.
ArrowOct 26, 2017 - Stop using nowFood
Whole Foods Market recalls Frosted Pumpkin Drop Cookies; 2-oz.; sold in clear plastic clamshell container with PLU number 024767; UPC 24767000000
Whole Foods Market recalls 2-oz. Frosted Pumpkin Drop Cookies due to undeclared walnuts. Check your clear clamshell containers for PLU 024767.
Whole Foods MarketOct 26, 2017 - Use cautionFood
Working Cow Homemade Inc. recalls Cookies N Cream Ice Cream 3 gallons
Working Cow Homemade recalls 3-gallon Cookies N Cream Ice Cream produced on 08/30/2017 due to Listeria monocytogenes found in environmental samples. Consumers should check product dates and contact the company for details.
Working Cow HomemadeOct 26, 2017 - Lower riskFood
Wegmans Food Markets, Inc. recalls Wegmans Large Cheese Filled Cannoli, 2 Pack, 5 oz UPC: 0-77890-37951 Wegmans Large Cheese Cannoli, 4 Pack, 10 oz UPC:
Wegmans recalls large cheese cannoli packs sold before October 26, 2017 due to undeclared soy lecithin. Consumers should check UPCs and contact Wegmans for details.
WegmansOct 26, 2017 - Lower riskMeat & poultry
FSIS Issues Public Health Alert for Poultry Products Due to Possible Listeria Contamination
U.S. Food Safety Service alerts that Mary's Harvest Fresh Foods poultry products may be contaminated with Listeria monocytogenes. Consumers are urged not to consume these products as they are past their Best by dates and no longer in commerce.
Mary's Harvest Fresh FoodsOct 25, 2017 - Use cautionVehicle
BMW 328I (2011) recall — Electrical System
BMW is recalling certain 2011 328i vehicles with overheating wiring that could cause electrical fires. Owners must have wiring replaced free by dealers.
BMWOct 25, 2017 - Use cautionVehicle
KEYSTONE COUGAR (2018) recall — Equipment
Keystone is recalling 2017-2018 Cougar western edition trailers due to stabilizer jacks that may detach during transit, posing a crash risk. Owners must have jacks inspected and fastened by dealers.
KeystoneOct 25, 2017 - Use cautionVehicle
AUDI A5 (2018) recall — Structure
Audi recalls certain 2018 A5 Sportbacks due to loose aluminum speaker trim that exposes sharp edges. Free dealer replacement available.
AudiOct 25, 2017 - Use cautionMedical device
Zimmer Biomet, Inc. recalls fastener, fixation, nondegradable, soft tissue
Zimmer Biomet recalls certain soft tissue implants due to improper assembly causing shaft shift and potential device breakage. Affected items include specific model numbers and lot numbers listed in the recall notice.
Zimmer BiometOct 25, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide inserts, Item Number: 816209003,UDI: 00887868044670989403
Zimmer Biomet recalls A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide inserts with incorrect color anodization. Affected items have specific item numbers and package lots. No immediate action needed.
Zimmer BiometOct 25, 2017 - Use cautionMedical device
Diagnostica Stago, Inc. recalls STA - Neoplastine¿ Cl Plus ¿ (ref. 00606) Product Usage: Manual or automated determination of the prothrombin time (PT).
Diagnostica Stago recalls Neoplastine Cl Plus reagent vials with confirmed defect causing prolonged prothrombin time (PT) readings. Affected lots expire 2018-2019. Stop using if you have these lots.
Diagnostica StagoOct 25, 2017 - Lower riskDrug
Teva Pharmaceuticals USA recalls Dutasteride and Tamsulosin HCl Capsules, 0.5 mg/ 0.4 mg, packaged in a) 30-count bottle (NDC 0591-3771-30), b) 90-count
Teva Pharmaceuticals USA recalls Dutasteride and Tamsulosin HCl capsules due to failed dissolution tests. All lots within expiry are affected. No remedy specified in recall notice.
Teva Pharmaceuticals USAOct 25, 2017 - UnratedDrug
Fagron, Inc recalls Estriol, For Prescription Compounding, packaged in a) 1 G bottle (NDC: 51552-1392-1), b) 5 G bottle (NDC:
Fagron recalls prescription estriol bottles due to quality assurance failures at the API manufacturer. This affects specific bottle sizes and lot numbers. Consumers should contact Fagron for details.
FagronOct 25, 2017 - Lower riskFood
E & E Enterprises recalls Cheesey Pizza Dip, Muriel's brand, dry mix, packaged in 1 pint glass jar. Cheesey Pizza Dip, Muriel's brand, dry mix,
E & E Enterprises recalls Cheesey Pizza Dip (Muriel's brand) dry mix for not listing milk and FD&C colors on labels. Consumers should check jars for missing ingredients.
E & E EnterprisesOct 25, 2017 - Stop using nowConsumer product

PlanToys Recalls Baby Gyms Due to Strangulation Hazard
PlanToys recalls baby gyms with side rope crossbars that pose strangulation risk for infants. Consumers must stop using and return for free replacement.
PlanToysOct 25, 2017 - Stop using nowConsumer product

Diving Unlimited International Recalls Scuba Diving Regulators Due to Drowning Hazard (Recall Alert)
Diving Unlimited International recalls scuba regulators with serial numbers 57792121-57814403 due to malfunction risk of drowning. Consumers must stop using and return for refund.
Diving Unlimited InternationalOct 25, 2017 - Use cautionVehicle
FORD F-150 (2017) recall — Power Train
Ford is recalling certain 2017 F-150 vehicles with ten-speed transmissions due to a risk of rolling or not moving when shifting. Owners must contact Ford for a free repair.
FordOct 24, 2017 - Use cautionVehicle
JEEP COMPASS (2018) recall — Engine And Engine Cooling
Chrysler recalls 2018 Jeep Compass models with 2.4L engines due to potential oil pump housing cracks causing engine stalling and crash risk. Owners must have oil pump inspected and replaced free by dealers.
ChryslerOct 24, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Persona Partial Knee Spacer Blocks To assist in partial knee arthroplasty surgery
Zimmer Biomet recalls Persona Partial Knee Spacer Blocks (sizes 8-14mm) for potential tightness during range-of-motion testing and looseness in final trial, which may affect surgery outcomes.
Zimmer BiometOct 24, 2017 - Stop using nowMedical device
Windstone Medical Packaging, Inc. recalls AMS, ALIGNED MEDICAL SOLUTIONS, T&A Pack, AMS6357, STERILE EO.
Windstone Medical recalls sterile surgical kits AMS6357 with potential sterile barrier breach. Affected kits include Lot #109138. Stop using immediately to avoid infection risks.
Windstone MedicalOct 24, 2017 - Lower riskMedical device
Radiometer America Inc recalls ABL800 analyzer with FLEXQ module. Device intended for in vitro testing of samples of whole blood for the parameters
Radiometer recalls ABL800 blood analyzers with FLEXQ module that may display incorrect patient results due to barcode misinterpretation. Affected units have specific serial numbers.
RadiometerOct 24, 2017 - Lower riskMedical device
Arrow International Inc recalls Pneumothorax Kit
Arrow recalls Pneumothorax Kit (AK 01500 CA 0150: Packaging may not be completely sealed. Consumers should check packaging for seal integrity.
ArrowOct 24, 2017 - Lower riskMedical device
Medtronic Minimally Invasive Therapies Group recalls Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is an extruded tube used as an extension for
Medtronic recalls Argyle Suction Tubing (Product #8888301515) due to possible incorrect labeling in one lot, which may lead to confusion with Salem Sump Dual Lumen Stomach Tube. This affects surgical tubing used in operating rooms.
Medtronic Minimally Invasive Therapies GroupOct 24, 2017 - Lower riskMedical device
Smith & Nephew, Inc. recalls smith&nephew TRIGEN INTERTAN 10S, REF 71675384, 10 MM X 18 CM NAIL, 130o (degrees), SET SCREW PREASSEMBLED IN NAIL
Smith & Nephew recalls a specific lot of TRIGEN INTERTAN 10S nails due to a screw being inserted upside down, which could cause improper installation.
Smith & NephewOct 24, 2017 - Lower riskMedical device
Howmedica Osteonics Corp. recalls radial stem implant #3 (Sterile packed). Orthopedic implant for replacement of the proximal end of the radius in the
Howmedica recalls radial stem implant #3 (Sterile packed) due to higher revision rates than other proximal radial head replacements. This implant may not perform as expected post-surgery.
HowmedicaOct 24, 2017 - Lower riskMedical device
Medacta Usa Inc recalls The GMK knee system: designed for cemented use in total knee arthroplasty. Sphere and Primary Inserts with part number
Medacta recalls GMK knee implants with a small risk of screw back-out after surgery. Affected models include specific part numbers and serial numbers for cemented total knee replacements.
MedactaOct 24, 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.