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
34,959 found- Use cautionConsumer product
RH Recalls Callum Canopy Beds Due to Injury Hazard (Recall Alert)
RH recalls Callum canopy beds due to risk of horizontal rails detaching and falling, potentially causing injury. Affected models sold with specific SKUs and colors; contact RH for free in-home repair.
RHApr 18, 2019 - Stop using nowConsumer product
Arctic Cat Recalls Snowmobiles Due to Fire Hazard (Recall-Alert)
Arctic Cat recalls 2018-2019 snowmobiles with fire risk from exhaust flaring. Stop using immediately and contact for free repair.
Arctic CatApr 18, 2019 - Use cautionVehicle
LIVIN' LITE CAMPLITE (2017) recall — Structure
Livin' Lite is recalling 2013-2017 Camplite and 2014-2017 Bearcat trailers with blocked exit windows that could prevent escape during emergencies.
Livin' LiteApr 17, 2019 - Use cautionVehicle
HYUNDAI VELOSTER (2019) recall — Latches/Locks/Linkages
Hyundai recalls 2019 Veloster vehicles with potential driver door ejection risk in crashes. Owners must have door latch assembly replaced free by dealers.
HyundaiApr 17, 2019 - Lower riskMedical device
Remel Inc recalls Thio Med w/o Ind, w/Dex (18ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose
Remel recalls Thio Med w/o Ind w/Dex 20-pack due to shortened expiration date (105 days) from 9 months to prevent performance failures in testing.
RemelApr 17, 2019 - Lower riskMedical device
Angiodynamics Inc. (Navilyst Medical Inc.) recalls AngioDynamics Solero Microwave Tissue Ablation (MTA) System: Solero Generator PG (1) Catalog Number:12740000 UPN:
Angiodynamics recalls Solero Generator PG units with specific serial numbers to reduce risk of procedure delays. Updated software and manual instructions help ensure safe use during medical procedures.
AngiodynamicsApr 17, 2019 - Lower riskMedical device
Remel Inc recalls Thio Med w/Dex, Hem, Vit K (5ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general
Remel recalls Thio Med w/Dex, Hem, Vit K (5ml) 100/PK products with shortened expiry dates due to potential failure in performance testing after 57 days.
RemelApr 17, 2019 - Lower riskFood
Healthy Life Snacks, Inc. recalls Healthy Life Snacks- Tropical Trail Mix 4 oz Polypropylene bag UPC code 2362918909
Healthy Life Snacks recalls Tropical Trail Mix 4oz bags (UPC 2362918909) sold from April 2018 to April 2019 due to undeclared sulfur dioxide. Consumers should check product dates and contact the company for details.
Healthy Life SnacksApr 17, 2019 - Stop using nowConsumer product
MTD Recalls Lawn Mowers Due to Injury Hazard; Sold Exclusively at Lowe's (Recall Alert)
Craftsman M350 lawn mowers with model 12ABR2BK793 recalled due to sharp collecting bag that can pierce and injure users during operation. Stop using immediately and contact Craftsman for free repair.
CraftsmanApr 17, 2019 - Stop using nowConsumer product
Heat Hero Recalls Portable Plug-in Heaters Due to Fire and Burn Hazards (Recall Alert)
Heat Hero recalls 350W plug-in ceramic space heaters due to fire and burn risks. Consumers must stop using and return for free replacement.
Heat HeroApr 17, 2019 - Stop using nowConsumer product
Go Couture Recalls Children's Loungewear Due to Violation of Federal Flammability Standard
Go Couture recalls children's loungewear sets that fail federal flammability standards, risking burn injuries. Consumers must stop using and get a refund.
Go CoutureApr 17, 2019 - Use cautionVehicle
FLEETWOOD FLAIR (2019) recall — Equipment
REV recalls 2019 Fleetwood Flair Model 32 S motorhomes due to generator exhaust pipe placement that may cause carbon monoxide leaks if driven on inclines. Owners must have exhaust rerouted by dealers.
REVApr 16, 2019 - Lower riskMedical device
OCULOGICA recalls EyeBOX Model OCL 02
OCULOGICA recalls EyeBox Model OCL 02 with serial numbers TT003, TT004, TT005 due to missing precaution statements in user manual.
OCULOGICAApr 16, 2019 - Lower riskMedical device
Zimmer Surgical Inc recalls Zimmer Biomet Alvarado Knee Holder Base Plate Assembly and Foot Piece, & Alvarado II Base Plate and Foot Piece:
Zimmer Biomet recalls Alvarado Knee Holder Base Plate Assembly and Foot Pieces due to potential foreign material from inadequate cleaning. Affected items have specific item numbers and were sold with all lot codes.
Zimmer BiometApr 16, 2019 - Lower riskMedical device
Ad-Tech Medical Instrument Corporation recalls AD-TECH Spencer Probe Depth Electrode Product Usage: The Ad-Tech Depth Electrodes (Depth Electrodes, Foramen Ovale
Ad-Tech recalls Spencer Probe Depth Electrodes with incorrect contact count that may cause improper brain mapping during surgery. The recall addresses a manufacturing error where some units were labeled as 8-contact but are actually 6-contact.
Ad-TechApr 16, 2019 - Lower riskFood
Denali Ingredients LLC recalls Banana Puddin Base, item # 70 0559-1034, in 5 gallon plastic pail. Net Wt: 48 LBS. Ice Cream Flavoring. Store
Denali Ingredients LLC recalls Banana Puddin Base (item #70 0559-1034) due to undeclared egg sub-ingredient. Products sold in 5-gallon plastic pails with specific lot numbers and expiration dates.
Denali IngredientsApr 16, 2019 - Use cautionVehicle
TRIUMPH THRUXTON 1200R (2017) recall — Electrical System
Triumph recalls certain 2016-2018 Thruxton 1200R motorcycles due to electrical issues that may cause headlight or turn signal failure, increasing crash risk. Owners must have wire conduits replaced free.
TriumphApr 15, 2019 - Lower riskMedical device
Abbott Gmbh & Co. KG recalls Alinity c Cuvette Segments, List Number 04S47-01 Product Usage: The Alinity c Cuvettes are used on the Alinity c system
Abbott recalls Alinity c Cuvette Segments (List 04S47-01) due to potential inadequate sample dispensing. Affected units may cause inaccurate test results. Contact Abbott for details.
AbbottApr 15, 2019 - Use cautionMedical device
Hitachi America, Ltd., Power Systems Division recalls PROBEAT-V, software versions 4.8.1S, and 5.1M Radiation therapy system.
Hitachi recalls specific software versions of its PROBEAT-V radiation therapy systems due to potential target position discrepancies in 3D3D matching mode. Affected units may require correction to prevent treatment errors.
HitachiApr 15, 2019 - Use cautionMedical device
Med Tec Inc recalls CIVCO Solstice(TM) SRS Immobilization System, Part Numbers: a) CHS03, b) CHS04 - Product Usage: The Tilting Head
Med Tec recalls Solstice Tilting Head Fixation System (part numbers CHS03/CHS04) due to potential movement during patient setup or treatment. Affected units include specific lot numbers and UDI codes.
Med TecApr 15, 2019 - Lower riskDrug
Iso-Tex Diagnostics, Inc recalls Volumex (Iodinated I 131 Albumin) Injection USP, 25 uCi per 1 mL syringe, Rx Only, Manufactured for Daxor Corp., NY,
Iso-Tex Diagnostics recalls Volumex (Iodinated I 131 Albumin) Injection due to lack of sterility assurance. This risks infection from contaminated product. Patients should contact their doctor for guidance.
Iso-Tex DiagnosticsApr 15, 2019 - Stop using nowFood
Jensen Tuna Inc recalls Frozen ground tuna, 1 lb package, 20 packages/case
Jensen Tuna Inc recalls frozen ground tuna due to potential Salmonella contamination. Check lot codes Z266, Z271, Z272.
Jensen TunaApr 15, 2019 - Lower riskFood
LE CAFE DE LA PLAGE recalls Le Cafe de la Plage Malibu Black Vanilla; Hand-Crafted Ice Cream 1 Pint PETE plastic twist top container:
Le Cafe de la Plage recalls Malibu Black Vanilla 1-pint ice cream with PETE plastic twist top containers due to plastic pieces found in the product. Consumers should check lot numbers and contact the company for details.
Le Cafe de la PlageApr 15, 2019 - Lower riskFood
Unilever recalls Ben & Jerry s Coconut Seven Layer Bar Bulk . The product is sold in a tub containing 2.4 gallons .
Unilever recalls Ben & Jerry's Coconut Seven Layer Bar bulk and Chunky Monkey pints due to undeclared tree nuts, brazil nuts, hazelnuts, and almonds in the ingredient list.
Ben & Jerry'sApr 15, 2019 - Stop using nowFood
Juices International, Inc. recalls All Juice Drinks and Beverages in 12 ounce glass bottles including but not limited to Agony, Double Trouble, Front End
Juices International recalls all produced juices due to FDA shutdown letter. Includes Agony, Double Trouble, and others distributed in NY.
All JuiceApr 15, 2019 - Stop using nowConsumer product
H&M Recalls Children's Bathrobes Due to Violation of Flammability Standard (Recall Alert)
H&M recalls children's hooded bathrobes that fail flammability standards, risking burns. Affected items include gray robes with white/pink or white/blue lining and white cat-embroidered robes. Consumers should stop using and get a refund.
H&MApr 15, 2019 - Stop using nowFood
Schreiber Foods Inc recalls Shredded and blocks of Colby & Monterey Jack cheese - Labeled and Packaged: 1) Great Value, Finely Shredded, Colby &
Schreiber Foods recalls Great Value, HeluvaGood, and other Colby & Monterey Jack cheese products due to hard plastic contamination.
Great ValueApr 14, 2019 - Lower riskFood
Mondelez Global Llc recalls Chewy Chips Ahoy Cookie (13 OZ)
Mondelez recalls 13oz Chewy Chips Ahoy cookies due to possible foreign material. Consumers should check UPC 044000032234 for affected products.
MondelezApr 13, 2019 - Stop using nowMeat & poultry
Denver Processing LLC Recalls Raw Pork and Beef Products Produced Without Benefit of Inspection
Denver Processing LLC recalls ~13,865 lbs of raw pork and beef produced without federal inspection. Do not consume; return or discard.
Denver ProcessingApr 12, 2019 - Use cautionVehicle
VOLKSWAGEN PASSAT (2015) recall — Air Bags
Volkswagen is recalling 2015 Passat vehicles with driver's side air bag inflators that may explode due to propellant degradation, risking serious injury or death. Owners must have the inflators replaced free of charge.
VolkswagenApr 12, 2019
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,516 recalls tracked · 71,994 explained in plain English · 10,968 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.