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
35,004 found- Lower riskMedical device
Elekta Impac Software recalls MOSAIQ, oncology information system - Product Usage: MOSAIQ is an oncology information system used to manage workflows
Elekta recalls specific versions of MOSAIQ oncology software where users might accidentally enter metric values in height/weight fields labeled in US units. This could lead to incorrect treatment calculations.
Elekta ImpacSep 24, 2019 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls SOMATOM go.Top, Models 11061640 & 11061648- a Computer tomography x-ray system
Siemens recalls two models of SOMATOM go.Top CT scanners due to missing dose documentation and dose alert features during interventional procedures, which could lead to radiation exposure risks.
SiemensSep 24, 2019 - Lower riskMedical device
Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc. recalls 4Fr x 20cm Single Lumen CT Midline Basic Tray, Product Code: VYML4S1001
Churchill Medical Systems recalls 4Fr x 20cm Single Lumen CT Midline Basic Tray (Product Code VYML4S1001) due to risk of using 3Fr catheters instead of 4Fr, which could cause complications.
Churchill Medical SystemsSep 24, 2019 - Lower riskDrug
Amneal Pharmaceuticals, Inc. recalls Benazepril HCl Tablets, USP 40 mg, 100 count bottles, Rx only, Distributed by Amneal Pharmaceuticals, Bridgewater, NJ
Amneal Pharmaceuticals recalls 40mg Benazepril tablets due to foreign promethazine tablets found in some bottles. This could cause unintended medication intake. Contact for return instructions.
Amneal PharmaceuticalsSep 24, 2019 - UnratedDrug
Apotex Inc. recalls Equate Maximum Strength Ranitidine Tablets, USP 150 mg Acid Reducer 130 Tablets Distributed by Wal-Mart Stores, Inc.
Apotex recalls 150mg ranitidine tablets due to possible N-nitrosodimethylamine (NDMA) contamination. Consumers should check NDC numbers and contact Apotex for details.
ApotexSep 24, 2019 - Lower riskFood
Wismettac Asian Foods, INC recalls Nori Ajitsuke 100P SK 8.81 oz. (250 g) UPC 074410528288 Item #52818
Wismettac Asian Foods recalls Nori Ajitsuke 100P SK 8.81 oz. due to incorrect seafood species listed on labels, containing skipjack tuna and krill.
Wismettac Asian FoodsSep 24, 2019 - Use cautionFood
Massey Fish Company recalls Massey Fish Company Smoked Whitefish Pate, in a refrigerated 8 oz. plastic tub, with UPC number 854656007018
Massey Fish Company recalls smoked whitefish pate with Listeria Monocytogenes detected in samples. Products sold with UPC 854656007018 and lot #2699 are unsafe and must not be consumed after 9/24/2019.
Massey Fish CompanySep 24, 2019 - Lower riskFood
Sara Lee Frozen Bakery recalls Chef Pierre ¿ SMALL WHOLE GRAIN BANANA MUFFINS NET WT 12 LB (5.44kg) 4 TRAYS/24/2 oz WHOLE GRAIN BANANA MUFFINS KEEP
Sara Lee recalls 12-lb frozen banana muffins due to tree nut foreign material. Consumers should check lot codes and contact for details.
Sara LeeSep 24, 2019 - Stop using nowConsumer product
Home Meridian Recalls Three-Drawer Chests Due to Tip-Over and Entrapment Hazards
Home Meridian recalls Mid-Century three-drawer chests due to tip-over and entrapment risks. Stop use if unanchored; get free restraint kit or refund.
Home MeridianSep 24, 2019 - Use cautionVehicle
PLEASURE WAY PLATEAU (2018) recall — Equipment
Pleasure Way is recalling 2018-2020 Plateau motorhomes with Fiamma awnings due to risk of unintended extension causing injury or crash. Owners must contact customer service for free fixes.
Pleasure WaySep 23, 2019 - Use cautionVehicle
SPARTAN GLADIATOR (2020) recall — Service Brakes, Air
Spartan recalls 2020 Gladiator vehicles with unsecured air brake lines that could cause sudden brake failure. Owners must have lines rerouted to prevent crashes.
SpartanSep 23, 2019 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH 930 Analyzer
Siemens Healthcare recalls Atel:lica CH 930 analyzers with software V1.20.0 and lower due to potential calibration errors causing QC results to be 5x higher than expected. Affected units have specific serial numbers and software versions.
Siemens HealthcareSep 23, 2019 - Lower riskMedical device
Randox Laboratories, Limited recalls RANDOX NEFA (Non-Esterified Fatty Acids) FA115 Lot 485343, GTIN: 5055273203066.
Randox recalls NEFA FA115 Lot 485343 due to not meeting performance claims. This batch should not be used in testing. Check your product details to confirm if affected.
RandoxSep 23, 2019 - Lower riskMedical device
Tomtec Imaging Systems Gmbh recalls TOMTEC-ARENA TTA2;software version no. 2.20 and lower; Picture archiving and communications system. Software Versions
Tomtec recalls ARENA TTA2 software versions 2.20 and lower due to potential mixing of study data between 3D applications. Affected units may store measurements from one study to another, risking incorrect medical results.
TomtecSep 23, 2019 - Lower riskDrug
AuroMedics Pharma LLC recalls Ranitidine Tablets USP,150 mg, 8-count bottles, Distributed by: Dolgencorp, LLC, 100 Mission Ridge, Goodlettsville, TN
AuroMedics Pharma recalls 150mg Ranitidine tablets due to empty bottles in one lot. Consumers should check NDC 55910-092-79 and lot number NBSB19001DA3 for affected products.
AuroMedicsSep 23, 2019 - UnratedDrug
Macleods Pharma Usa Inc recalls Pioglitazone Hydrochloride Tablets USP 15 mg, 30 count bottles, Rx only, Manufactured for: Macleods Pharma USA, Inc.,
Macleods Pharma recalls 15mg Pioglit: Superpotent risk in 30-count bottles. Rx only. Check NDC 33342-054-07 and lot BPF901A.
MacleodsSep 23, 2019 - UnratedDrug
Morton Grove Pharmaceuticals, Inc. recalls Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, packaged in a 8 fl oz (237 mL) bottle, Rx only, Manufactured
Morton Grove Pharmaceuticals recalls Prednisolone Sodium Phosphate Oral Solution due to failed impurity specifications. This medication, sold Rx only, may contain harmful impurities that could affect safety.
Morton Grove PharmaceuticalsSep 23, 2019 - UnratedDrug
Sandoz, Inc recalls Sandoz Ranitidine Hydrochloride Capsules 150mg 60 Capsules Rx Only Manufactured by Sandoz Inc. Princeton, NJ Product of
Sandoz recalls 150mg ranitidine capsules due to trace N-nitrosodimethylamine (NDMA) impurity. This may pose health risks. Consumers should contact Sandoz for details.
SandozSep 23, 2019 - Lower riskDrug
Unipharma, Llc. recalls DrKids Himasal Natural Nasal Saline Solution, packaged in Pre-measured Singe-Use Vials a) 0.5 mL Each (20 count) UPC
Unipharma recalls DrKids Himasal Natural Nasal Saline Solution vials due to potential contamination with bacteria B. cepacia. Affected products have specific UPCs and expiration dates.
DrKidsSep 23, 2019 - Stop using nowFood
Scenic Fruit Company recalls Frozen Organic Blueberries Packed into Poly Bag, Net Weight 3 lbs. Product of USA. Item 815544, Kirkland Signature
Kirkland Signature frozen organic blueberries (3 lb bags) recalled due to foreign material contamination. Check your freezer for Item 815544.
Kirkland SignatureSep 23, 2019 - Lower riskFood
Basic Reset Inc. recalls Bee Gold 8oz. pkg./plastic pouch, SKU: 100-4C
Basic Reset recalls Bee Gold 8oz plastic pouches due to failure to meet dietary supplement manufacturing regulations. Consumers should check product codes for affected items.
Basic ResetSep 23, 2019 - Lower riskFood
California New foods recalls Carolyn's Cookie Company - Frozen Cookie Doughballs - Bake at Home. Chocolate Chip Net Wt. 22 oz. (623.7g) UPC Code
Recall of Carolyn's Cookie Company Frozen Cookie Doughballs (22 oz) from April 7, 2019 to March 29, 2020 due to reported allergic reactions. Check lot codes for affected items.
Carolyn's Cookie CompanySep 23, 2019 - Lower riskMedical device
Blue Ortho recalls Blue Ortho TKA Pro v2.1 software installed on the Exactech GPS system -indicated for stereotaxic surgery in Knee
Blue Ortho recalls TKA Pro v2.1 software for Exactech GPS knee surgery systems due to incorrect navigated values. Affected users should contact Blue Ortho for updates.
Blue OrthoSep 22, 2019 - Stop using nowMeat & poultry
Astrochef LLC. Recalls Chicken Pub Style Entrees Due to Misbranding and Undeclared Allergens
Marie Callenders recalls frozen pub style steak and ale entrees due to undeclared soy allergens. Check your freezer for lot code 5659916910.
Marie CallendersSep 20, 2019 - Use cautionVehicle
DUCATI 1299 (2016) recall — Engine
Ducati recalls 2014-2018 1299 models due to oil leaks from airbox drain hose that may cause crashes. Owners must contact for free blow-by valve kit installation.
DucatiSep 20, 2019 - Use cautionVehicle
TOYOTA 4RUNNER (2019) recall — Steering
Southeast Toyota recalls 2018-2019 Toyota 4Runners with loose steering fasteners that could cause loss of control or road hazards. Owners must have dealers inspect and re-tighten components free of charge by November 19, 2019.
Southeast ToyotaSep 20, 2019 - Use cautionVehicle
FOREST RIVER CHEROKEE (2020) recall — Electrical System
Forest River recalls 2020 Cherokee trailers with exposed wiring in storage compartments that could cause electrical shock or fire. Owners must have a divider installed by dealers to protect wiring.
Forest RiverSep 20, 2019 - Use cautionVehicle
FOREST RIVER SABRE (2020) recall — Electrical System
Forest River recalls 2019-2020 Sabre trailers with electrical short risk causing fire or brake failure. Owners must have pin box contact with junction box.
Forest RiverSep 20, 2019 - Lower riskDrug
Akorn, Inc. recalls Phenylephrine Hydrochloride Ophthalmic Solution, USP, 2.5%, 15 mL bottle, Rx only, Mfd. by: Akorn, Inc., Lake Forest,
Akorn recalls 2.5% phenylephrine eye drops (15mL) for possible contamination. The product may not be sterile, posing a risk of infection. Consumers should contact Akorn for details.
AkornSep 20, 2019 - Use cautionFood
Euphoria Fancy Food Inc recalls Capitan K Salmon slightly salted piece - net.wt 1.05 oz (200g) Distributed by: Euphoria Fancy Food Inc. 149-151 2nd
Euphoria Fancy Food Inc recalls Capitan K Salmon slightly salted pieces (1.05 oz) due to potential Listeria monocytogenes contamination. Consumers should check UPC 607059000362 and return affected products.
Euphoria Fancy FoodSep 20, 2019
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