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- Lower riskMedical device
Riverpoint Medical, LLC recalls Riverpoint Medical 18G Brachy Grid, B&K style, REF RPG-18, Sterile, Rx. The firm name on the label is Riverpoint
Riverpoint Medical recalls 18G Brachy Grid (RPG-18) due to potential sterile packaging compromise. Affected units have specific lot numbers and UDI. Consumers should contact for details.
Riverpoint MedicalFeb 8, 2019 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop Omnia Max is a device intended to visualize
Siemens recalls Uroskop Omnia Max fluoroscopy systems with serial numbers 4032-5078 due to risk of swivel arm dislodging, potentially causing injury during medical imaging procedures.
SiemensFeb 8, 2019 - Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls Cardiohelp Emergency Drive, Part No. 70104.8002 Product Usage: The Cardiohelp Emergency Drive is used in emergencies to
Maquet recalls specific Cardiohelp Emergency Drive models due to potential incorrect reassembly during servicing, which may cause inadequate operation in emergencies. Affected serial numbers listed.
MaquetFeb 8, 2019 - Lower riskMedical device
Elekta, Inc. recalls Monaco Radiation Treatment Planning (RTP) System
Elek: Monaco radiation treatment software version 5.40 may use incorrect dose optimization models during plan adaptation. Affected users should contact Elekta for details.
ElektaFeb 8, 2019 - Use cautionMedical device
Canon Medical System, USA, INC. recalls Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) - Product Usage: The catheterization table is
Canon Medical recalls Infinix DP-i (CAT-870B) catheterization tables that tilt unexpectedly when liquid spills into the tilt console, potentially causing patient falls. Affected models were sold from 2005-2008.
Canon MedicalFeb 8, 2019 - Use cautionMedical device
Draegar Medical Systems, Inc. recalls Infinity Delta Family patient monitors The Infinity Delta Series (Delta/Delta XL/Kappa) monitors are intended to be
Draegar Medical Systems recalls Infinity Delta Series patient monitors due to cybersecurity vulnerabilities that may cause device reboots, loss of function, and communication issues. Affected models include Delta, Delta XL, and Kappa monitors.
Draegar Medical SystemsFeb 8, 2019 - Lower riskMedical device
Terumo Medical Corporation recalls Terumo Sur-vet Needle, 25G x 5/8", Product Code 100280
Terumo recalls 25G x 5/8" Sur-vet Needles (Product Code 100280) due to potential loss of sterility. Affected lot numbers: 180814C, 181002C, 181009C.
TerumoFeb 8, 2019 - Stop using nowDrug
McDaniel Life-Line LLC recalls Indian Herb Paste (a dietary supplement) Ingredients: Galangal, Indian Paint, Yellow Dock & Licorice in an alloy of
McDaniel Life-Line recalls Indian Herb Paste dietary supplement containing unapproved ingredients. This product poses a drug safety risk and should not be used.
McDaniel Life-LineFeb 8, 2019 - Lower riskDrug
Avella of Deer Valley, Inc. Store 38 recalls MAGnesium 2 gm sulfate, added to NS 50 mL, Sterile single use bag, 54 mL, Compounded by Avella Specialty Pharmacy 24416
Avella recalls magnesium sulfate solution due to incorrect expiration dates on product labels, which may lead to medication safety issues if used after the wrong expiry date.
AvellaFeb 8, 2019 - Lower riskFood
World Waters, LLC dba WTRMLN WTR recalls Watermelon, WTRMLNWTR Cold Pressured, 12fl oz, Watermelon Flavor, Refrigerated
World Waters recalls 12-packs of cold-pressed watermelon juice due to soft plastic pieces that may float in some bottles. Consumers should check lot numbers listed to see if their product is affected.
World WatersFeb 8, 2019 - Use cautionVehicle
VOLVO VNL (2019) recall — Electrical System
Volvo recalls 2019 VNL trucks with faulty transmission fuse that may prevent shifting, risking crashes. Owners must contact Volvo Trucks for free fuse replacement.
Volvo TrucksFeb 7, 2019 - Use cautionVehicle
VOLVO VNL (2019) recall — Power Train
Volvo is recalling 2019-2020 VNL trucks with potential air tank strap deformation causing risk of tank dropping and crash. Free replacement of straps available.
Volvo TrucksFeb 7, 2019 - Stop using nowVehicle
FREIGHTLINER SPRINTER 4500 (2019) recall — Visibility
Freightliner and Mercedes-Benz Sprinter vans recalled for side windows that may not prevent occupant ejection in crashes. Free glass replacement available.
FreightlinerFeb 7, 2019 - Lower riskMedical device
Randox Laboratories Ltd. recalls Liquid Immunoassay Premium Controls, Model Number LIA3105 Product Usage: This product is intended for in vitro
Randox recalls LIA3105 liquid immunoassay controls for inaccurate test results. The target value is listed incorrectly on the value sheet, potentially causing inaccurate lab diagnostics.
RandoxFeb 7, 2019 - Lower riskMedical device
Cordis Corporation recalls Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for
Cordis recalls specific lots of Vista Brite Tip & Androit Guiding Catheters due to frayed mounting card pieces in primary packaging. No remedy is stated in the recall notice.
CordisFeb 7, 2019 - Lower riskDrug
ACP Nimble Buyer, Inc. recalls Mometasone Furoate Cream, 0.1%, 45 g tube, Rx Only, Manufactured by: G&W Laboratories, Inc. South Plainfield, NJ 07080,
ACP Nimble Buyer recalls Mometasone Furoate Cream 0.1% due to an NDC typographical error on the label. Check your lot numbers and expiration dates.
ACP Nimble BuyerFeb 7, 2019 - Lower riskFood
Willamette Valley Pie Company, LLC. recalls Frozen IQF Red Raspberries packed in a flexible polybag. Each bag is 2 lbs (906.5g), 6 bags per case. UPC is 0 22518
Willamette Valley Pie Company recalls frozen raspberries due to potential Hepatitis A virus contamination. Consumers should check UPC 022518877509 for affected lots.
Willamette Valley PieFeb 7, 2019 - Stop using nowFood
Birdseed Food Co LLC recalls Craft Granola Goldenola Turmeric & Ginger, packaged in 3 oz. and 11 oz. poly bag, UPC: 860157002028 and 8601570020135
Birdseed Food Co LLC recalls Craft Granola Goldenola Turmeric & Ginger due to undeclared cashews. Check UPCs and expiration dates.
Craft GranolaFeb 7, 2019 - Use cautionFood
Kingston Pharma LLC recalls DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (120 mL) Liquid Dietary
Kingston Pharma recalls DG Baby Gripe Water herbal supplements due to undissolved citrus flavonoid. This may cause choking or digestive issues in infants. Check product UPC 8 54954 0:00246 3 for affected lots.
Kingston PharmaFeb 7, 2019 - Stop using nowConsumer product
Delta Electronics Recalls Solar Inverters Due to Fire and Impact Hazards
Delta Electronics recalls Eltek THEIA HE-t solar inverters due to fire and impact risks from capacitor failure. Stop using immediately.
EltekFeb 7, 2019 - Lower riskMedical device
Medica Corporation recalls Medica Wash1-Wash solution used prior to Lipase assay on the EasyRA clinical chemistry analyzer REF 10680 - Product
Medica recalls Wash1-Wash solution for EasyRA analyzers due to interference with Lipase tests. Affected lots 18066, 18133, :18235, 18317. No remedy specified.
MedicaFeb 6, 2019 - Lower riskMedical device
Advanced Bionics, LLC recalls Na¿da CI Q70 Sound Processor, Sand Beige, Model Cl-5245-120; Silver Gray, Model Cl-5245-140; and Velvet Black, Model
Advanced Bionics recalls Q70 Sound Processors with Sand Beige, Silver Gray, and Velvet Black models due to incorrect firmware loading. Affected units may not function properly.
Advanced BionicsFeb 6, 2019 - Use cautionMedical device
LW Scientific, Inc. recalls LW Scientific ZIP IQ PCV Centrifuge, ZIC-24HD-75T3 Rev C Product Usage: used as a general purpose centrifuge to spin
LW Scientific recalls ZIP IQ PCV Centrifuge model ZIC-24HD-75T3 Rev C due to risk of plastic rotor breaking during use and being ejected, potentially causing injury to technicians.
LW ScientificFeb 6, 2019 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Esomeprazole Magnesium Delayed-Release Capsules USP, 40mg*, a) 90-count bottle (NDC 43598-510-90) b) 1000 count bottle
Dr. Reddy's recalls 40mg esomeprazole capsules with brown pellets. Discoloration may indicate unsafe product. Check NDC codes for affected lots.
Dr. Reddy'sFeb 6, 2019 - Lower riskDrug
Advanced Pharma Inc. recalls Fentanyl in 0.9% Sodium Chloride QS 0.5 mL, 5 mcg/0.5 mL with up to 0.1 mL of overfill Injectable Solution, Sterile
Advanced Pharma recalls Fentanyl injectable solution with incorrect expiration date labeling. This may lead to medication errors if used after the wrong expiration date. Contact the manufacturer for details.
Advanced PharmaFeb 6, 2019 - UnratedDrug
Advanced Pharma Inc. recalls Oxytocin 20 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1002 mL
Advanced Pharma recalls oxytocin injectable solution with potential higher oxytocin concentrations than labeled. This may cause unsafe effects during medical use. Check product details to determine if affected.
Advanced PharmaFeb 6, 2019 - Lower riskDrug
Ecolab Inc recalls Express Gel Hand Sanitizer (Ethyl Alcohol 70%), 37 mL (1.25 fl oz) bottles, Ecolab, 370 Wabasha Street N, St. Paul, MN
Ecolab recalls 37mL hand sanitizer bottles due to low levels of substituted benzene compounds causing malodor. Consumers should check product details and contact Ecolab for guidance.
EcolabFeb 6, 2019 - Stop using nowConsumer product
Dell Recalls Hybrid Power Adapters Sold with Power Banks Due to Shock Hazard
Dell recalls hybrid power adapters sold with power banks due to risk of electric shock from casing breaking and detaching. Consumers must stop using and get free replacements.
DellFeb 6, 2019 - Lower riskMeat & poultry
Richwell Group, Inc. Recalls Siluriformes Products Produced Without Benefit of Import Inspection
USDA FSIS recalls 73,360 pounds of Siluriformes fish products imported from Vietnam without import inspection. Consumers urged not to consume or dispose of these products.
Maxfield SeafoodFeb 5, 2019 - Use cautionVehicle
SUZUKI KIZASHI (2013) recall — Air Bags
Suzuki is recalling 2010-2013 Kizashi vehicles with a front air bag that may not deploy in a crash due to misclassifying adult occupants as children.
SuzukiFeb 5, 2019
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