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
35,021 found- Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Siemens Dimension Vista Akaline Phosphatase (ALPI) Flex reagent cartridge - In vitro diagnostic test for the
Siemens recalls Dimension Vista ALPI Flex reagent cartridges that may produce low outlier results. Affected lots have expired or were sold between 2009-2020. No action needed for low risk results.
Siemens HealthcareAug 25, 2020 - Lower riskMedical device
Medtronic Vascular recalls Rashkind Balloon Septostomy Catheter, 6F, Recess Balloon, Closed end, 50 cm, Pediatric, Single Lumen Product number:
Medtronic Vascular recalls pediatric Rashkind Balloon Septostomy Catheters (6F, 50 cm) due to field failures and failed quality testing. Affected lot numbers include GFCP2154 through GFDZ1693. Consumers should contact Medtronic for details.
Medtronic VascularAug 25, 2020 - Lower riskMedical device
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x3/32, Catalog Number 5791 - Product Usage: intended for
Terumo recalls air sensors for extracorporeal procedures due to wiring causing false alarms. Check serial numbers 20019-20020 for affected units.
TerumoAug 25, 2020 - UnratedDrug
Asiaticon, SA de CV recalls V-Klean Hand Sanitizer Gel Alcohol 70% packaged as a)8.5 fl oz (250 ml), UPC 7 16053 70499 3; b) 16.9 fl oz (500 ml),
Asiaticon recalls V-Klean Hand Sanitizer Gel Alcohol 70% due to lack of current good manufacturing practices (CGMPs). Affected products include 250ml and 500ml bottles with specific UPCs. Consumers should contact the manufacturer for details.
AsiaticonAug 25, 2020 - Use cautionDrug
RLC Labs Inc. recalls WP Thyroid, Westhroid Pure, 1 Grain (65 mg) Thyroid USP, packaged in a) 1,000 Tablets, NDC 64727-5750-2 ; b) 30
RLC Labs recalls certain lots of WP Thyroid and Westhroid Pure due to potential subpotency from CGMP deviations. Check your NDC and expiry date.
RLC LabsAug 25, 2020 - Stop using nowFood
Taylor Farms Retail Inc recalls Taylor Farms BBQ Ranch Chopped Kit Salade Coupee Chili Lime Tortilla Squares, Bacon & BBQ Ranch Dressing NET WT 277 g
Taylor Farms recalls BBQ Ranch Chopped Kit due to undeclared wheat and sesame. Check your product if purchased in Canada.
Taylor FarmsAug 25, 2020 - Lower riskFood
Keurig Dr Pepper, Inc. recalls Newman's Own Organics, Newman's Special Decaf Medium Roast, Ground Coffee, 10 oz.
Newman's Own recalls organic decaf coffee that contains regular non-organic coffee due to packaging mix-up. Consumers should check product codes and contact the company for details.
Newman's OwnAug 25, 2020 - Use cautionMedical device
Boston Scientific Corporation recalls Opticross 35 15 MHz Peripheral Imaging Catheter 8F (2.74 mm) X 105 cm Expiration Date June 8th 2021 - July 22nd 2021
Boston Scientific recalls Opticross 35 15 MHz Peripheral Imaging Catheters with flaking markings that could cause embolization during use. Return all affected units to the manufacturer immediately.
Boston ScientificAug 24, 2020 - Use cautionMedical device
Alcon Research, LLC recalls Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health" PROTEXIS" Latex Micro Surgical Gloves - Product
Alcon Research recalls specific Custom-Pak Surgical Procedure Packs containing PROTEXIS latex micro surgical gloves due to potential holes at cuff folds that could increase infection or cross-patient exposure risk.
Alcon ResearchAug 24, 2020 - Lower riskMedical device
Exactech, Inc. recalls Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 22 mm.
Exactech recalls Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 22 mm due to possible incorrect screw length. Affected units have specific serial numbers. Contact Exactech for details.
ExactechAug 24, 2020 - Lower riskMedical device
Smith & Nephew, Inc. recalls EVOS Screws - Product Usage: is a part of the EVOS MINI plating system, indicated for fracture fixation, arthrodesis,
Smith & Nephew recalls EVOS Screws with incorrect expiration dates on labels. These screws are used in bone repair procedures. Affected parts include specific model numbers and batch lots.
Smith & NephewAug 24, 2020 - Lower riskMedical device
Irvine Biomedical Inc, a St. Jude Medical Co. recalls Inquiry Steerable Diagnostic Catheter, REF: IBI-81104 - Product Usage: INDICATIONS FOR USE The Inquiry fixed curve and
Irvine Biomedical recalls steerable diagnostic catheters with incorrect model numbers that could cause procedure delays if misused. Affected units include specific batch numbers.
Irvine BiomedicalAug 24, 2020 - Use cautionMedical device
Imactis recalls Imactis Patient Fiducial (Patient Referential), REF: IHR-YY-XXX component used in conjunction with the
Imactis recalls patient fiducial components used with CT navigation workstations due to separation risks causing navigation inaccuracies. All units are affected.
ImactisAug 24, 2020 - Lower riskDrug
Strides Inc. recalls Strides Pharma Inc.Potassium Chloride Extended-Release Tablets, USP 8mEq (600 mg) 100 Tablets Rx Only Manufactured by:
Strides Pharma Inc. recalls potassium chloride extended-release tablets due to failed dissolution specifications. This may affect medication effectiveness. Check NDC 64380-860-06 or 7240675A.
StridesAug 24, 2020 - Lower riskDrug
Teva Pharmaceuticals USA recalls Cephalexin for Oral Suspension, USP 250 mg per 5 mL, For Reconstitution, For Oral Use Only, Rx Only, a) 100 mL bottle
Teva Pharmaceuticals USA recalls specific lots of Cephalexin oral suspension due to potential active ingredient levels outside specifications. Consumers should check their product details and contact the company for guidance.
Teva PharmaceuticalsAug 24, 2020 - Lower riskFood
Frito-Lay, Inc. recalls Frito-Lay 28 count Classic Cube Mix cube box UPC 28400 15586 1 oz. individual bags packaged in a larger non-flexible box
Frito-Lay recalls 28-count Classic Cube Mix bags due to potential undeclared milk content. Consumers should check product UPC 28400 15586 for affected items.
Frito-LayAug 24, 2020 - Use cautionMeat & poultry
Oberto Snacks, Inc. Recalls Smoked Sausage Products Due to Misbranding and an Undeclared Allergen
USDA recalls Oberto Smoked Sausage products from March 2020 due to soy allergen not listed on labels. Consumers urged to stop using recalled items.
Oberto SnacksAug 22, 2020 - Stop using nowFood
Russ Davis Wholesale, LLC recalls Peach Salsa, Keep Refrigerated packed in the following size containers and brands: 1. Crazy Fresh, Net Wt. 8 oz UPC
Russ Davis Wholesale recalls Peach Salsa products from 6/25/2020 to 8/26/2020 due to possible Salmonella contamination. Consumers should check UPC codes and stop using if contaminated.
Russ Davis WholesaleAug 22, 2020 - Use cautionVehicle
AUTOCAR XPEDITOR (2019) recall — Equipment
Autocar is recalling 2019 Xpeditor vehicles with aftermarket PTO systems that may stall or hesitate when operated from the right side stand up position, increasing crash risk.
AutocarAug 21, 2020 - Use cautionVehicle
THOR MOTOR COACH WINDSPORT (2020) recall — Electrical System
Thor is recalling certain 2019-2021 Windsport motorhomes due to a damaged circuit board that could cause fire. Owners should contact Thor for free repairs.
ThorAug 21, 2020 - Use cautionVehicle
FORD EXPLORER (2020) recall — Air Bags
Ford is recalling 2020 Explorer vehicles with potential side air bag deployment issues due to improper seat back fastening. Owners must have front seat back panels checked by dealers for free.
FordAug 21, 2020 - Lower riskMedical device
North American Rescue LLC. recalls 4 In. Flat Responder Emergency Trauma Dressing part number 30-0171, packaged in kits labeled as follows: a) M-FAK Mini
North American Rescue recalls 4-In. Flat Emergency Trauma Dressing kits (part number 30-0171) due to lack of sterility assurance. Affected kits include various M-FAK Mini and Trauma First Aid Kits with specific product codes and lot numbers listed.
North American RescueAug 21, 2020 - Use cautionMedical device
Handicare AB recalls SwiftHook sold as the following: a. Individually as SwiftHook b. Included with Vega505EE mobile lifts Product Usage:
Handicare AB recalls SwiftHook components for mobile lifts that may detach during use, posing a risk of injury. Affected units include specific model numbers and serials.
HandicareAug 21, 2020 - Lower riskFood
Frito-Lay, Inc. recalls Ruffles Original Potato Chips NET WT 1 1/2 oz. packaged in flexible bags UPC 28400 48228
Frito-Lay recalls Ruffles Original Potato Chips with undeclared milk. Check for UPC 28400 48228 and use by date 22 SEP 2020.
Frito-LayAug 21, 2020 - Lower riskFood
Cedar's Mediterranean Foods, Inc. recalls Cedar's Cucumber Garlic Dill Tzatziki, 12 oz packaged in clear plastic tubs; Made with GREEK YOGURT; INGREDIENTS:
Cedar's Mediterranean Foods recalls 12oz cucumber garlic dill tzatziki tubs made with Greek yogurt due to undeclared food starch, gelatin, and natamycin. Consumers should check UPC 099482481643 for affected products.
Cedar'sAug 21, 2020 - Lower riskFood
Lac O' Seasons Resort,Inc recalls SCHAWS SWEET WITH HEAT BARBECUE AND BASTING SAUCE, 18oz glass jar, UPC code 7 93573 11599
Lac O' Seasons Resort recalls 18oz glass jars of Sweet Heat BBQ Sauce with use by date 8/20/2022 or earlier due to undeclared soy and anchovies.
Lac O' Seasons ResortAug 21, 2020 - Stop using nowFood
Wegmans Food Markets, Inc. recalls Wegmans Vanilla Trifle; 9oz; UPC 7789080600
Wegmans recalled 9oz Vanilla Trifles sold Aug 16-21, 2020 due to potential Salmonella Enteritidis contamination from raw peaches.
WegmansAug 21, 2020 - Stop using nowConsumer product
woom bikes USA Recalls Children's Helmets Due to Risk of Head Injury (Recall Alert)
Woom bikes USA recalls small children's helmets that fail federal safety standards. Stop using them now and contact the company for a full refund.
WoomAug 21, 2020 - Use cautionVehicle
BMW R 1250 RT (2021) recall — Equipment
BMW recalls 2021 R 1250 RT motorcycles with detachable tire pressure labels that could lead to improper tire inflation and crash risks. Owners must have labels replaced by dealers.
BMWAug 20, 2020 - Lower riskMedical device
Roche Diagnostics Operations, Inc. recalls Elecsys Anti-TPO Assay on cobas e analyzers 411, 601, 602, Catalog Number 06368590190
Roche recalls Elecsys Anti-TPO Assay for cobas e 411/601/602 analyzers due to RF interference claims not meeting standards. All current and upcoming lots affected.
RocheAug 20, 2020
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