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
Westlab Pharmacy, Inc. dba Westlab Pharmacy recalls Cyclosporine 1% Human Eye Drops, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-2776-92
Westlab Pharmacy recalls Cyclosporine 1% Human Eye Drops (NDC 10002-2776-92) because of lack of process controls. This may affect safety for people with eye conditions.
Westlab PharmacyAug 10, 2018 - Lower riskMedical device
Rayner Intraocular Lenses Limited recalls C-flex 570C +19.0D Intraocular Lens Product Usage: C-flex IOLs are designed to be surgically implanted into the
Rayner recalls C-flex 570C +19.0D intraocular lenses due to reported post-operative refractive errors after implantation. Affected lenses have specific batch numbers.
RaynerAug 9, 2018 - Lower riskMedical device
Besmed Health Business Corporation recalls Ambu Aura40 Standard, Reusable Laryngeal Mask Catalog Number: 340300000
Besmed Health recalls Ambu Aura40 Standard reusable laryngeal masks due to potential infection risk from improper sterilization. Affected units have specific catalog and lot numbers.
Besmed HealthAug 9, 2018 - Lower riskMedical device
Biomet UK Ltd. recalls HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 3 Hole Plate Item Number: 2110-135-003
Biomet recalls HipLOC Hip Fracture Fixation System plates with undersized barrel that may prevent lag screw fit. Affected items have specific item numbers and lot numbers. Contact for remedy.
BiometAug 9, 2018 - Use cautionDrug
Orexigen Therapeutics, Inc. recalls Contrave (naltrexone HCl and bupropion HCl) Extended-Release Tablets, 8 mg/90 mg, 120-count bottle, Rx only,
Orexigen recalls Contrave 8mg/90mg tablets due to customer reports of bottle punctures. Affected lots expire Nov 2020. Stop using if you have these bottles.
OrexigenAug 9, 2018 - Lower riskFood
MORTON SALT INC recalls MORTON NATURAL SEA SALT ALL PURPOSE***NET WET 26 OZ (1 LB 10 OZ) 737 g***Nutrition Facts***INGREDIENTS: SEA SALT
Morton Natural Sea Salt All-Purpose 26 oz packages recalled due to iodized salt packaging. Consumers should check product labels for the specific batch.
MortonAug 9, 2018 - Lower riskFood
Deli Star Ventures Inc. dba King's Food Products recalls Chef s Request professional steak marinade and Buckhead wildlife marinade, 12oz, 64oz, 1 gallon; shelf stable,
King's Food Products recalls Chef s Request steak marinade and Buckhead wildlife marinade due to undeclared soy and wheat allergens. Consumers should check product labels for production dates and lot codes.
King's Food ProductsAug 9, 2018 - Stop using nowConsumer product
Vitamix Recalls Ascent and Venturist Series Blending Containers Due to Laceration Hazard
Vitamix recalls Ascent and Venturist blending containers due to laceration risk. Check your blade date code and stop using if affected.
VitamixAug 9, 2018 - Stop using nowConsumer product
Harbor Freight Tools Recalls Handgun Safes Due to Serious Injury Hazard
Harbor Freight Tools recalls Union Safe Company and Bunker Hill Security handgun safes. They may open without a key upon impact, posing injury risks. Return for a refund.
Harbor Freight ToolsAug 9, 2018 - Use cautionVehicle
FREIGHTLINER CASCADIA (2019) recall — Steering
Daimler Trucks North America recalls 2018-2019 Freightliner Cascadia trucks with potential pitman arm fractures causing loss of steering control. Owners must have pitman arms replaced free by dealers starting October 6, 2018.
Daimler Trucks North AmericaAug 8, 2018 - Lower riskMedical device
Magellan Diagnostics, Inc. recalls Magellan LeadCare¿ II Blood Lead Test Kit. In Vitro Test for the measurement of lead in fresh whole blood. Catalog
Magellan recalls LeadCare II Blood Lead Test Kit (lot 1808M) due to calibration button defect causing false high lead levels. This affects professional blood lead testing devices.
MagellanAug 8, 2018 - Lower riskMedical device
Medtronic Perfusion Systems recalls Extra corporeal circuit with bio-active surface.
Medtronic Perfusion Systems recalls extra corporeal circuits with bio-active surfaces that failed sterilization tests. Affected units may pose infection risks.
Medtr: a short, human brand name for headings (e.g. "Trsmima")Aug 8, 2018 - Lower riskMedical device
Helena Laboratories, Corp. recalls ColoCARE, Cat. No. 5651, packaged 50 envelopes/box, For In-Vitro Diagnostic Use. The firm name on the label is Helena
Helena Laboratories recalls ColoCARE diagnostic kits with faulty positive control that may not react properly during testing. Affected kits have specific lot numbers and expiration dates.
HelenaAug 8, 2018 - Use cautionMedical device
Philips North America LLC recalls Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758
Philips recalls infant/child defibrillator pads due to incorrect age labeling on packaging. Using these on adults may cause ineffective shock delivery. Affected units have model M5072A.
PhilipsAug 8, 2018 - Lower riskMedical device
Implant Direct Sybron Manufacturing, LLC recalls ImplantDirect Legacy 3 Implant, REF 855216, SBM implant assembly, 2mmD x 16mmL, 4.5mmD platform, Rx, Sterile. The
Implant Direct recalls Legacy 3 implants with mislabeled vial caps (part number 835216) that could lead to incorrect usage. Affected units have a specific model and lot number.
Implant DirectAug 8, 2018 - Use cautionMedical device
Bausch & Lomb Inc recalls Bausch + Lomb Stellaris Elite Vision Enhancement System, 20 ga. Posterior Wide-Field Elite Pack, REF SE5420W
Bausch & Lomb recalls Stellaris Elite 20 GA Vitrectomy Cutters with risk of back cap separating from the body during use, potentially causing injury. Affected units have specific lot numbers and expiration dates.
Bausch & LombAug 8, 2018 - Use cautionMedical device
Olympus Corporation of the Americas recalls Bronchovideoscope BF-XP160F
Olympus recalls Bronchovideoscope BF-XP1:160F due to potential loosening of the instrument channel port when non-Olympus accessories are attached. All units are affected.
OlympusAug 8, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 130 11 mm x 340 mm, Item Number 814511340 Product Usage: Intended for the fixation of
Zimmer Biomet recalls Affixus Hip Fracture Nails with lot number 369640 due to sterile packaging opening during surgery. Affected patients should contact the company for details.
Zimmer BiometAug 8, 2018 - UnratedDrug
Hetero Labs Limited Unit V recalls Camber Pharmaceuticals, Inc. Valsartan Tablets, USP, 320 mg, 90 tablets, Rx Only Manufactured for: Camber
Hetero Labs Limited Unit V recalls Camber Pharmaceuticals Valsartan 320mg tablets due to detected carcinogen impurity in manufacturing. Affected lots expire 7/2018 to 6/2020. Stop using immediately.
Hetero Labs Limited Unit VAug 8, 2018 - UnratedDrug
Akorn, Inc. recalls Azelastine HCl Ophthalmic Solution 0.05%, 6 mL in 10 mL HDPE bottle, 1 bottle per box, Rx only, Manufactured by: Akorn,
Akorn recalls 0.05% Azelastine HCl Ophthalmic Solution 6mL bottles due to impurities that could cause harm. This prescription eye drop is sold in HDPE bottles with specific lot numbers and expiration dates.
AkornAug 8, 2018 - Lower riskFood
Morgan Foods, Inc. recalls Tomato Condensed Soup, 26 oz (1 LB 10 OZ) 737 g, 307 x 512 Can, Family Size, 12 cans per tray, shelf stable
Morgan Foods recalls 26oz tomato soup due to mislabeling containing undeclared milk and soy allergens. Consumers should check for batch code E2918 on cans.
Morgan FoodsAug 8, 2018 - Use cautionConsumer product
Polaris Recalls Gravely Utility Vehicles Due To Fire and Burn Hazards (Recall Alert)
Recall of 2015-2018 Gravely Atlas JSV 3000/6000 utility vehicles due to exhaust pipe cracking causing fire and burn risks. Affected models sold in red with specific serial numbers.
GravelyAug 8, 2018 - Use cautionConsumer product
Bobcat Company Recalls Utility Vehicles Due To Burn and Fire Hazards (Recall Alert)
Polaris Industries recalls 2015-2018 Bobcat 3400 and 3400XL utility vehicles due to exhaust pipe cracking causing burn and fire risks. Owners must contact authorized dealers for free repairs.
BobcatAug 8, 2018 - UnratedMedical device
Medtronic Inc. recalls Minimed Model 503 Remote Transmitter (MMT-503, MMT-503EU, MMT-503NA, MMT-503US) for use with the MiniMed Paradigm
Medtronic recalls Minimed Model 503 Remote Transmitters for potential security risks with insulin pumps. Affected units may have vulnerabilities that could compromise patient safety.
MedtronicAug 7, 2018 - Lower riskMedical device
Implant Direct Sybron Manufacturing, LLC recalls ImplantDirect simply RePlant Implant, size 4.3mmD x 13mmL, 4.3mmD Platform, REF 604313U, Rx, Sterile. The firm name on
ImplantDirect recalls a specific size 4.3mmD x 13mmL implant due to incorrect packaging in vials. Affected units have a specific lot number and label details. Consumers should contact the manufacturer for guidance.
Implant DirectAug 7, 2018 - Lower riskDrug
PD-Rx Pharmaceuticals, Inc. recalls Doxycycline Hyclate USP Tablets, 100 mg packaged in a) 2-count bottles, NDC 55289-866-02; b) 6-count bottles, NDC
PD-Rx Pharmaceuticals recalls 100mg Doxycycline Hyclate tablets with failed dissolution tests. These may not work as intended. Check NDC codes and expiration dates for affected lots.
PD-Rx PharmaceuticalsAug 7, 2018 - Stop using nowDrug
Mylan Pharmaceuticals Inc. recalls Diltiazem HCl Extended-Release Capsules, USP 120 mg 100-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown,
Mylan recalls 120mg Diltiazem capsules due to impurities found in stability testing. This may cause serious injury. Stop using immediately and contact Mylan for details.
MylanAug 7, 2018 - Lower riskFood
Vidalia Valley, Inc. recalls Boar's Head Brand Sweet Vidalia Onions in Sauce, glass jars 9oz UPC 0 42421 06956 3 & 64 oz UPC 0 42421 26517 0.
Boar's Head recalls sweet vidalia onions in sauce due to glass contamination. Consumers should check UPCs and stop using if glass is found.
Boar's HeadAug 7, 2018 - Lower riskFood
Graeters Manufacturing Company recalls Graeter's HANDCRAFTED French Pot ICE CREAM, Limited Edition KEY LIME PIE**ONE PINT (473 ml)**Nutrition Facts**GLUTEN
Graeter's Limited Edition Key Lime Pie Ice Cream is recalled for containing wheat despite being labeled gluten-free. This poses a risk for people with celiac disease or gluten allergies. Consumers should check packaging for the product code and contact Graeter's for details.
Graeter'sAug 7, 2018 - Stop using nowFood
Natures Bounty Inc recalls BLUE GREEN ALGAE: Packaged under the following brands: AMERICAN HEALTH KALMATH SHORES BLUE GREEN ALGAE, 120 CAPSULES,
Natures Bounty recalls blue green algae supplements due to high microcystin levels. Products sold under American Health Kalmath Shores and Puritan's Pride brands contain unsafe levels of this toxin.
Natures BountyAug 7, 2018
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