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- Stop using nowFood
Marsee Foods Inc recalls Chocolate Chip Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each master case contains
Marsee Foods recalls Cafe YUMM! chocolate chip cookies due to undeclared peanuts. Check lot codes and dates if you dine at affected Oregon or Washington restaurants.
Cafe YUMM!Aug 15, 2018 - Stop using nowFood
Sammy Food Products LLC recalls Sammy Salsa Happy Medium, packaged in 14 oz. plastic container, 6 units per case. UPC # 00868422000110. The label is
Sammy Food Products LLC recalls Sammy Salsa Happy Medium due to potential Cyclospora contamination. Check your UPC and use-by date.
Sammy Food ProductsAug 15, 2018 - Stop using nowConsumer product
Xtava Recalls Allure Hair Dryers Due to Fire, Burn and Electrical Shock Hazards
Xtava recalls Allure and Allure Pro hair dryers due to fire, burn and electrical shock risks from overheating. Consumers must stop using and get a free replacement.
XtavaAug 15, 2018 - Lower riskMedical device
Lens.com recalls Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile.
Lens.com recalls Alcon Air Optix Night & Day Aqua contact lenses with specific lot numbers for potential microbial issues. Consumers should check labels for counterfeit risks.
Lens.comAug 14, 2018 - Use cautionMedical device
Ohio Medical Corporation recalls Portable Suction Pump, (a) Style 758010, Model CARE-E-VAC 3, Ohio Medical LLC; (b) Style 758000, Model CARE-E-VAC 3,
Ohio Medical recalls CARE-E-VAC 3 portable suction pumps with serial numbers starting CDS0081 to CEV3X0499 due to battery terminal short circuit risk causing loss of function or inoperable unit under battery power.
Ohio MedicalAug 14, 2018 - Use cautionMedical device
Tec Com Gmbh recalls TECOTHERM NEO, 100-130/200-240 VAC, 50-60 Hz/ max. 350VA, Class I, Schutzklasse I IP 20, UDI: 04260498580002 - Product
Tec Com recalls TECOTHERM NEO devices with faulty peltier elements that could fail to maintain temperature during therapy. Affected units were manufactured between September 7 and October 5, 2018.
Tec ComAug 14, 2018 - Use cautionMedical device
Siemens Healthcare Diagnostics, Inc. recalls APTIO 15000 REFRIGERATED STORAGE MODULE
Siemens Healthcare recalls APTIO 15000 refrigerated storage modules that may lack pacemaker warning labels, risking interference with medical devices. Affected units have specific Siemens material numbers.
Siemens HealthcareAug 14, 2018 - UnratedDrug
Mckesson Corporation recalls Megestrol Acetate Oral Suspension, USP 400 mg/mL, 10 mL (10 mL UD cups in boxes of 20 cups), Rx Only, Mfg. By: Par
Mckesson recalls Megestrol Acetate Oral Suspension (400 mg/mL, 10mL) due to supert potent drug risk. Rx-only product with specific lot numbers and expiration dates. Contact for return or disposal instructions.
MckessonAug 14, 2018 - Lower riskDrug
United Therapeutics Corp. recalls Tyvaso Inhalation System Patient a) Starter Kit with TYVASO (treprostinil) Inhalation Solution. Treprostinil 1.74
United Therapeutics recalls Tyvaso inhalation system starter kits with water ingress risk. Defective device may cause improper medication delivery. Consumers should contact for remedy.
United TherapeuticsAug 14, 2018 - Lower riskDrug
Mylan Institutional, Inc. (d.b.a. UDL Laboratories) recalls Diltiazem HCl Extended-release Capsules, USP 120 mg, 80 capsules, 8 blister cards of 10 capsules each per carton, Rx
Mylan recalls 120mg diltiazem capsules due to impurities. This may cause harm. Check your prescription for NDC 51079-947-08, batch 3096049.
MylanAug 14, 2018 - UnratedDrug
Jubilant Cadista Pharmaceuticals, Inc. recalls Valsartan Tablets USP, 320 mg, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd Roorkee 0247661 India,
Jubilant Cadista recalls 320mg Valsartan tablets due to potential incorrect excipient used in manufacturing. Affected lots from Roorkee, India. No specific remedy stated in official notice.
Jubilant CadistaAug 14, 2018 - UnratedDrug
AVKARE Inc. recalls Valsartan Tablets, USP 40 mg Rx Only NDC 50268-783-15 50 Tablets (5x10) Unit Dose Manufactured for: AvKARE, Inc.
AVKARE recalls 40mg Valsartan tablets due to detected carcinogen impurity in manufacturing. Affected lots expire 10/2018 to 10/2019. No specific remedy provided in recall notice.
AVKAREAug 14, 2018 - Use cautionFood
SALT & STRAW LLC recalls Chocolate Gooey Brownie Ice Cream, packaged in pint-sized containers (473 mL), net wt 378 g; 1 gal. container, or 3
Salt & Straw recalls chocolate gooey brownie ice cream due to possible undeclared peanuts. Consumers should check lot numbers for affected products.
Salt & StrawAug 14, 2018 - Stop using nowConsumer product
Koehler-Bright Star Recalls Flashlights Due to Explosion Hazard
Koehler-Bright Star recalls WorkSafe 3-D cell flashlights without a date code stamp due to explosion risk. Consumers must stop using and check for missing date codes to avoid injury.
Koehler-Bright StarAug 14, 2018 - Use cautionVehicle
ROADTREK RS ADVENTUROUS (2017) recall — Fuel System, Diesel
Erwin Hymer is recalling 2017-2018 Roadtrek RS Adventurous motorhomes with a damaged diesel fuel tank that could leak fuel and cause fire. Owners must have the tank inspected and replaced free by dealers.
Erwin HymerAug 13, 2018 - Use cautionVehicle
FOREST RIVER XLR (2019) recall — Equipment
Forest River is recalling 2019 XLR recreational trailers due to potential awning deployment while moving, which could increase crash risk. Owners should contact customer service for free awning controller replacement.
Forest RiverAug 13, 2018 - Lower riskMedical device
Remel Inc recalls remel THIOGLYCOLLATE MEDIUM, REF 05152
Remel recalls THIOGLYCOLLATE MEDIUM REF 05152 due to intermittent failure in stability testing with anaerobic microorganisms. Affected lots include 258192.
RemelAug 13, 2018 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls IsoFlex LAL Support Surface, Model Number 2860 Product Usage: : The IsoFlex LAL support surface assists in the
Stryker recalls 2860 IsoFlex LAL Support Surfaces with non-conforming fire barrier. These medical devices for pressure injury prevention may pose fire risk if improperly used in healthcare settings.
StrykerAug 13, 2018 - Lower riskMedical device
Stryker Spine recalls AVS Aria Cage, Catalog Number 48753212 Product Usage: The Stryker Spine AVS¿ ARIA 1M PEEK Spacers are intervertebral
Stryker Spine recalls AVS Aria Cage (Catalog 48753212) due to anterior and posterior markers being on the wrong sides, potentially causing surgical errors. Affected patients should contact Stryker for guidance.
Stryker SpineAug 13, 2018 - Lower riskMedical device
bioMerieux, Inc. recalls VITEK(R) 2 AST-P655, For susceptibility testing of Staphylococcus spp. Enterococcus spp., ad S agalactiae against
BioMérieux recalls VITEK 2 AST-P655 test cards with insufficient gentamicin due to manufacturing error. Affected lots may produce inaccurate test results for bacterial susceptibility.
BioMérieuxAug 13, 2018 - Lower riskMedical device
Custom Healthcare Systems, Inc. recalls CHS Custom Convenience Kit-FOERSTER SPONGE FORCEPS, SERR, ST (9.5 ) Product Number:-D36-14623
Custom Healthcare Systems recalls convenience kits with foam forceps due to improper sterility packaging. Affected units may pose infection risks if used in medical procedures.
Custom Healthcare SystemsAug 13, 2018 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Lisinopril Tablets USP, 10mg, 1000-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals Inc. Baltimore,
Lupin Pharmaceuticals recalls 10mg Lisinopril tablets due to metal contaminant in one tablet. Consumers should check product details and contact for remedy.
Lupin PharmaceuticalsAug 13, 2018 - Stop using nowDrug
Living Well Remedies, LLC recalls Living Well Remedies Weight Away Remedy, 2 fl oz (59 mL) Distributed by Living Well Remedies, LLC P.O. Box 704,
Living Well Remedies recalls Weight Away Remedy due to microbial contamination. Check your lot number and expiration date for details on this Class I recall.
Living Well RemediesAug 13, 2018 - Lower riskFood
Howard Calcagno Farms recalls Red Leaf Lettuce was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR
Howard Calcagno Farms recalls Red Leaf Lettuce potentially contaminated with Cyclospora cayetanensis. Consumers should check for cardboard boxes labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
Howard Calcagno FarmsAug 13, 2018 - Lower riskMedical device
The Binding Site Group, Ltd. recalls VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kit For in vitro diagnostic use, Product Code:
The Binding Site Group recalls VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kits due to potential false positive results in immunodeficiency testing. Affected kits may show falsely elevated antibody levels.
The Binding Site GroupAug 12, 2018 - Use cautionVehicle
JEEP WRANGLER (2018) recall — Latches/Locks/Linkages
Chrysler recalls 2018 Jeep Wrangler models with potential rear passenger door opening risk. Owners must contact for free latch repair by December 6, 2018.
ChryslerAug 11, 2018 - Lower riskMedical device
Micro Therapeutics Inc, Dba Ev3 Neurovascular recalls ev3 TurboHawk PERPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE, LARGE VESSEL XTENDED TIP FOR CALCIUM, Model THS-LX-C
Ev3 recalls TurboHawk peripheral plaque excision system model THS-LX-C due to incompatible Distal Flush Tool accessories causing inability to remove excised material during surgery.
Ev3 NeurovascularAug 10, 2018 - Use cautionMedical device
A M Systems Inc recalls Disposable Smooth Interior Tubing Material: Polyethylene EVA copolymer. This tubing is supplied non-sterile P/N:
A M Systems recalls disposable smooth interior tubing (P/N 1024920 Rev. 01) that may pull apart when stretched. This tubing is used in ventilation and anesthesia machines. Affected units have specific lot numbers.
A M SystemsAug 10, 2018 - Lower riskMedical device
Medtest Holdings, Inc. recalls Pointe Scientific AutoHDL/LDL Cholesterol Calibrator, Catalog Number H7545-CAL - Product Usage: For the calibration of
Pointe Scientific recalls AutoHDL/LDL Cholesterol Calibrator (H7545-CAL) due to vials shipped without labels. This affects lab use and may cause misidentification of reagents.
Pointe ScientificAug 10, 2018 - UnratedDrug
RemedyRepack Inc. recalls Valsartan 160 mg Tablets, HDPE 90 cc bottles in cardboard trays, Rx Only, RemedyRepack, Inc., 625 Kolter Drive, Suite
RemedyRepack recalls Valsartan 160mg tablets with potential carcinogen impurity in the manufacturing process. Affected lots have specific expiration dates and NDC numbers. Consumers should contact the manufacturer for details.
RemedyRepackAug 10, 2018
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