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
34,943 found- UnratedDrug
Teva Pharmaceuticals USA recalls Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 160 mg/12.5 mg tablets, USP 90-count bottle, Rx Only, Rx Only,
Teva Pharmaceuticals USA recalls 90-count Valsartan/HCTZ tablets due to detected carcinogen impurity in manufacturing. This may pose cancer risk. Consumers should contact Teva for details.
Teva PharmaceuticalsJul 16, 2018 - UnratedFood
AMPI recalls AMPI Whey Powder, Sweet Type, Formula 521, Extra Grade, spray process pasteurized, packaged in 50 lbs net (22.68 kg
AMPI recalls Sweet Type Whey Powder Formula 521 due to potential Salmonella contamination. Affected lots include 7000.118.121.BL to 7000.118.165.BL. Consumers should check labels and contact AMPI for details.
AMPIJul 16, 2018 - Use cautionFood
General Mills, Inc recalls Cheerios Protein Oats & Honey, Packaged in the following sizes: Net Wt. 19 oz. (583g) UPC 16000-44473. 12 boxes/case,
General Mills recalls Cheerios Protein Oats & Honey cereal due to possible Salmonella contamination. Affected products include 19oz boxes with UPC 16000-44473 and 14.1oz boxes with UPC 16000-45137. Consumers should check labels and contact the company for details.
General MillsJul 16, 2018 - Lower riskFood
D & D Foods, Inc. recalls Hy-Vee Spring Pasta Salad packaged in the following containers: 1) plastic tubs with lids, Net Wt 16 OZ (454 g); 2)
Hy-Vee recalls spring pasta salad products from June 22, 2018 to August 3, 2018 due to potential Salmonella contamination. Consumers should check product dates and containers for affected items.
Hy-VeeJul 16, 2018 - Use cautionMeat & poultry
The Beautiful Pig, Inc. Recalls Ready-To-Eat And Raw Pork And Beef Products Produced Without The Benefit Of Inspection And Shipped Under U.S. Retention
USDA FSIS recalls ready-to-eat and raw pork/beef products from The Beautiful Pig Inc. that were produced without inspection and shipped under U.S. retention. Consumers urged not to consume these products.
The Beautiful PigJul 14, 2018 - Lower riskFood
Utz Quality Food Inc recalls utz Carolina Style Barbeque Potato Chips, Net Wt 2.875 OZ, UTZ Quality Foods, LLV, Hanover, PA 17301, UPC:
Utz is recalling certain batches of Carolina Style Barbeque Potato Chips due to undeclared soy allergen. Consumers should check product dates and UPCs for affected items.
UtzJul 14, 2018 - Lower riskFood
Aldi Inc recalls AnnaSea Wasabi Ahi Poke Hawaiian Poke Kits
Aldi recalls AnnaSea Wasabi Ahi Poke Hawaiian Poke Kits and Limu Ahi Poke Hawaiian Poke Kits that may have been stored above freezing, posing a food safety risk. Products with best by dates up to June 2020 are affected.
AldiJul 14, 2018 - Use cautionVehicle
VOLKSWAGEN TIGUAN (2018) recall — Visibility
Volkswagen recalls 2018 Tiguan vehicles with a risk of fire from a short-circuiting sunroof LED module. Owners must have the power supply disconnected by dealers until a safe fix is available.
VolkswagenJul 13, 2018 - Use cautionVehicle
FOREST RIVER PALOMINO (2019) recall — Equipment
Forest River is recalling 2019 Palomino campers with incorrect weight placard that could lead to overload and crash risk. Owners must get corrected placard for safety.
Forest RiverJul 13, 2018 - Lower riskMedical device
Exactech, Inc. recalls Tibial Alignment Guide, REF 351-10-00 Vantage Fixed Ankle system components for ankle replacements.
Exactech recalls Tibial Alignment Guide (REF 351-10-00 Vantage Fixed Ankle) due to incorrect Global Trade Item Number (GTIN). Affected units have GTIN 10885862525629 instead of 10885862525628.
ExactechJul 13, 2018 - UnratedMedical device
Tosoh Bioscience Inc recalls G8 Automated HPLC Analyzer - 723G8 Product Usage - In vitro diagnostic use for the quantitative measurement of %
Tosoh recalls G8 HPLC analyzers with software missing a 510K clearance for hemoglobin A1c testing in diabetes diagnosis. Affected units have specific serial numbers listed.
Tosoh Biosc: IncJul 13, 2018 - Lower riskMedical device
Smiths Medical ASD Inc. recalls Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, REF 4080P-2, Sterile,
Smiths Medical recalls Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes due to mislabeling. Check labels for incorrect firm name or lot numbers 3306404, 3314069, 3318698.
Smiths MedicalJul 13, 2018 - Use cautionMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls 2008T HEMODIALYSIS SYSTEM W/BIBAG, Part Number 190766, Applicable only with 2008T BlueStar Premium Upgrade Kit, Part
Fresenius Medical Care recalls 2008T Hemodialysis Systems with BlueStar Premium Upgrade Kit due to risk of disinfectant not fully removed during power failures, potentially contaminating patient dialysate.
Fresenius Medical CareJul 13, 2018 - Lower riskMedical device
Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical recalls Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution
Kerr Corporation recalls Regimen 28 Day Glutaraldehyde solution due to incorrect immersion time on labels. Product may not sterilize properly if used as instructed.
Kerr CorporationJul 13, 2018 - Use cautionMedical device
Haemonetics Corporation recalls Haemonetics OrthoPAT System-Integrated Set. Product Code: 1150H-00 OrthoPAT orthopedic perioperative autotransfusion
Haemonetics recalls OrthoPAT System-Integrated Set (Product Code 1150H-00) due to missing cannula in reservoirs, preventing blood from being processed. Affected units sold with Lot #1017049 and 1150H-00.
HaemoneticsJul 13, 2018 - Use cautionMedical device
Philips Electronics North America Corporation recalls Philips SureSigns VM 3/4/6/8 Patient Monitors, 863063 863064 863065 863066 863068 863077 863085 863086 863317 863287
Philips recalls SureSigns VM 3/4/6/8 patient monitors with lithium batteries that may overheat or ignite after exceeding 3-year life expectancy. Replace batteries every 3 years or after 300 charge cycles to prevent fire or injury.
PhilipsJul 13, 2018 - Stop using nowDrug
Prinston Pharmaceutical Inc recalls Solco Healthcare US Valsartan and Hydrochlorothiazide, USP, 160 MG/25 MG Tablets, 90-count bottle, Rx Only,
Prinston Pharma recalls Solco Healthcare US Valsartan and HCTZ tablets due to carcinogen impurity. Check your NDC and lot numbers.
Solco Healthcare USJul 13, 2018 - Lower riskFood
Holley Cold Storage Fruit & Produce Co., Inc. recalls Europe's Best Field Berry Mix 12/600g (Strawberries, Blueberries, Blackberries)
Holley recalls Europe's Best Field Berry Mix 12/600g (strawberries, blueberries, blackberries) due to possible Salmonella contamination. Products with lot numbers HP38130682SMF823 and HP38131682SMF823, UPC 871454036187, and best before May 2020 are affected.
HolleyJul 13, 2018 - Use cautionFood
Pepsico Inc recalls Diet Pepsi 7.5 oz cans, 6-pack. UPC on case label is 0 12000 16314 2. The product's case label is read in parts:
PepsiCo recalls Diet Pepsi 7.5 oz 6-packs due to undeclared aspartame. Check your UPC and use-by date for affected lots distributed in the Pacific Northwest.
Diet PepsiJul 13, 2018 - Lower riskFood
The Coca-Cola Company recalls Odwalla Superfood fruit smoothie 15.2 oz. (450mL) plastic bottle; Sold in 8 pack case Unit UPC: 000-14054-06405-5
Odwalla Superfood fruit smoothie bottles in Canada may contain tiny metal fragments. Recalled units have UPC 000-14054-06405-5. Consumers should check their bottles and contact Odwalla for details.
OdwallaJul 13, 2018 - Stop using nowFood
Whole Foods Market Group Inc. recalls CANDY DESSERT SHELL VANILLA PANIBOIS, 17 Ounce
Whole Foods Market recalls 17oz Vanilla Candy Dessert Shells made in Mid-Atlantic stores between May 25 and July 13 due to undeclared soy.
Whole Foods MarketJul 13, 2018 - Use cautionVehicle
KENWORTH T680 (2018) recall — Seat Belts
PACCAR recalls 2018 Kenworth T680 trucks with seat belt buckles that may separate during crashes, increasing injury risk. Owners must replace faulty buckles free of charge by February 28, 2019.
KenworthJul 12, 2018 - Use cautionVehicle
KEYSTONE RAPTOR (2019) recall — Equipment
Keystone recalls 2018-2019 Raptor trailers with a propane line risk that could cause fire if stored with flame lit. Owners get free replacement of the propane line.
KeystoneJul 12, 2018 - Use cautionMedical device
GE Healthcare, LLC recalls Revolution CT systems with the SmartStep Option The system is intended for head, whole body, cardiac and vascular X-ray
GE Healthcare recalls Revolution CT systems with SmartStep Option that may scan at incorrect locations, risking inaccurate imaging. Affected units were sold between 2019 and 2:00 PM on 2023-01-01.
GE HealthcareJul 12, 2018 - Use cautionMedical device
Baxter Healthcare Corporation recalls power cord for: (a) AMIA Automated PD Cycler, Product Code: 5C9320; (b) Kaguya PD System, Product Code: T5C8500
Baxter Healthcare recalls power cords for AMIA Automated PD Cycler and Kaguya PD System (Japanese distribution) due to socket detaching when unplugged. Affected units have specific product codes and serial numbers.
Baxter HealthcareJul 12, 2018 - Use cautionMedical device
Medical Components, Inc dba MedComp recalls SOFT-LINE DUO-FLOW DOUBLE LUMEN CATHETER/CATHETER SET; T94C T94M T96M T98M
MedComp recalls SOFT-LINE DUO-FLOW double lumen catheter sets (T94C, T9: 150 characters
MedCompJul 12, 2018 - Lower riskMedical device
Ultradent Products, Inc. recalls Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit
Ultradent recalls Enamelast Cool Mint dental varnish due to potential unpleasant flavor. Affected products include 200pk and 50pk Cool Mint kits with specific lot numbers. Consumers should check labels for the recall.
UltradentJul 12, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Peg Fully Threaded, Locking, 2.5mm x 10mm, Item Number 131212610 Orthopedic device used for stabilization and fixation
Zimmer Biomet recalls Peg Fully Threaded, Locking 2. 5mm x 10mm units due to a 22mm threaded peg found in some packages. This could cause improper fixation of bone fragments.
Zimmer BiometJul 12, 2018 - Lower riskMedical device
Ortho Clinical Diagnostics Inc recalls VITROS Immunodiagnostic Products - Folate Reagent Pack(10758750009237) 1513266
Ortho Clinical Diagnostics recalls VITROS Folate Reagent Packs due to potential biased test results when patients take biotin supplements below the indicated concentration in the instructions.
Ortho Clinical DiagnosticsJul 12, 2018 - UnratedMedical device
Orthosensor, Inc. recalls OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, REF ZBH-PSNCREF311-L.
Orthosensor recalls VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left models with fluid in posterior lateral corner post-surgery. Affected units have specific lot numbers and UDI.
OrthosensorJul 12, 2018
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