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
34,956 found- Lower riskMedical device
Ortho-Clinical Diagnostics recalls VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic use only. CATALOG #(s): 6801710 INTENDED USE: For
Ortho-Clinical Diagnostics recalls VITROS VALP Reagent Pack (catalog #6801710) due to negative bias results in valproic acid testing. Affected lots from 2017-2019 may cause inaccurate test results.
Ortho-Clinical DiagnosticsDec 11, 2018 - Use cautionMedical device
Baxter Healthcare Corporation recalls Kaguya Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution
Baxter recalls Kaguya Automated Peritoneal Dialysis Systems due to potential shortened dwell times during therapy cycles, which may affect treatment effectiveness.
BaxterDec 11, 2018 - Use cautionMedical device
Kimberly-Clark Corporation recalls U by Kotex¿ Sleek¿, Regular Tampons, 3 Count
Kotex recalls 3-count regular tampons that may come apart during removal. Stop using if you have these specific lot numbers.
KotexDec 11, 2018 - Lower riskDrug
KVK-Tech, Inc. recalls Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC
KVK-Tech recalls 500-count Oxybutynin Chloride Tablets (5mg) due to incorrect bar code labeling. This may cause confusion in prescription handling but does not pose a safety risk.
KVK-TechDec 11, 2018 - Lower riskDrug
Asclemed USA Inc. dba Enovachem recalls Dyural-40 Injection Kit, 1 Dose, Single Use Only, Rx only, Distributed by Enovachem Pharmaceuticals, Torrance, CA
Enovachem recalls Dyural-40 Injection Kits due to latex in stoppers. These kits contain sodium chloride 0.9% and were distributed with specific lot numbers. Affected users should contact the manufacturer for details.
EnovachemDec 11, 2018 - UnratedFood
Del Monte Research Center - Walnut Creek recalls Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn seasoned with Red & Green Peppers. NET WT 15.25 oz. (432 g);
Del Monte recalls Fiesta Corn with red and green peppers due to potential botulism risk from incorrect thermal processing. Products sold between August 2021 and September 2021 may be affected.
Del MonteDec 11, 2018 - Use cautionFood
Moonstruck Chocolate Company recalls Sea Salt Caramels Tumbled In Milk Chocolate, Moonstruck brand. The product sold in an individual resealable plastic
Moonstruck recalls Sea Salt Caramels Tumbled In Milk Chocolate due to potential hazelnut contamination not declared on label. Products sold in 4oz plastic bags with specific lot numbers and best by dates are affected.
MoonstruckDec 11, 2018 - Use cautionFood
Lipari Foods Operating Company, LLC recalls Inspired Organic Tahini Butter 16oz. plastic jar, 6 per case UPC #: 863669742564 refrigerate after opening
Lipari Foods recalls Inspired Organic Tahini Butter 16oz jars due to Listeria monocytogenes contamination. Refrigerate after opening to reduce risk.
Lipari FoodsDec 11, 2018 - Lower riskFood
DAHLICIOUS recalls DAHlicious ORGANIC Lassi India -Style DRINKABLE YOGURT, Grassland Plain, , 32 FL OZ (946 mL), UPC: 7 93573 01459 7
DAHLICIOUS recalls Grassland Plain 32 fl oz organic lassi yogurt due to improper pasteurization. Consumers should check UPC 7 93573 01459 7 and lot number 2018317-1 for affected products.
DAHLICIOUSDec 11, 2018 - Stop using nowConsumer product
Penn State Industries Recalls Woodworking Jaw Chuck Systems Due to Laceration Hazard
Penn State Industries recalls steel woodworking jaw chucks with model CSCBARR5 that can loosen and cause lacerations. Consumers must stop using and get a refund.
Penn State IndustriesDec 11, 2018 - Stop using nowConsumer product
Kubota Recalls Zero Turn Mowers Due to Injury Hazard (Recall Alert)
Kubota recalls 2017-2018 Z400 and Z700 series zero turn mowers due to rollover protective structure failure risk. Affected units may not protect operators in rollover accidents.
KubotaDec 11, 2018 - Stop using nowMeat & poultry
CTI Foods LLC, Recalls Ready-To-Eat Pork and Poultry Sausage Products due to Possible Foreign Matter Contamination
Jimmy Dean Heat n Serve sausage links are recalled due to possible metal contamination. Check your freezer for the specific use-by date and case code.
Jimmy DeanDec 10, 2018 - Use cautionVehicle
MAZDA CX-9 (2015) recall — Air Bags
Mazda recalls 2015 CX-9 vehicles with passenger air bag inflators that may explode in crashes, causing serious injury or death. Owners must have the inflator replaced free of charge by dealers.
MazdaDec 10, 2018 - Lower riskMedical device
ProSun International, LLC recalls ProSun Onyx 32 Sli Intensive (12 minutes) tanning bed, Model 32/1. Labeled as the following: PROSUN ONYX 32 SLI
ProSun recalls specific model tanning beds due to potential high UV output from quality control discrepancies. Affected units may pose skin damage risks; check serial numbers listed in the notice.
ProSunDec 10, 2018 - Lower riskMedical device
Luminex Corporation recalls VERIGENE Processor SP Model No. 10-0000-07. An in vitro diagnostic device intended for processing and identifying
Luminex recalls VERIGENE Processor SP Model 10-0000-07 due to potential incorrect test results from hybridization heater failure. Affected units may need repair or replacement.
LuminexDec 10, 2018 - Lower riskMedical device
Leica Biosystems Imaging, Inc. recalls Aperio CS2 CE IVD scanner instrument, scanner part #23CS100CE.
Leica Biosystems recalls Aperio CS2 CE IVD scanners with part #23CS100CE (serials 5899, 5902, 5986) due to potential incorrect sensor causing image analysis errors and visual issues.
Leica BiosystemsDec 10, 2018 - Use cautionMedical device
Smith & Nephew, Inc. recalls JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 3-4 , REF 74013987 The JOURNEY II XR Tibial Posterior Keel Punch is a
Smith & Nephew recalls certain Journey II XR Tibial Posterior Keel Punches due to higher than expected bone fracture risk during use. Affected units have specific batch numbers. Consumers should contact the company for details.
Smith & NephewDec 10, 2018 - Lower riskMedical device
Signature Orthopedics Pty Limited recalls Genius Knee Cemented Tibial Component Product Usage: Knee replacement component
Signature Orthopedics recalls Genius Knee Cemented Tibial Component due to product mix-up risk. Affected units have specific UDI and model numbers.
Signature OrthopedicsDec 10, 2018 - UnratedDrug
Gordon Laboratories recalls Monsel's (Ferric Subsulfate) Solution, 8 mL amber glass bottle, packaged as one dozen bottles with applicators per box,
Gordon Laboratories recalls Monsel's (Ferric Subsulfate) Solution due to higher iron content than labeled. This superpotent drug may cause serious health risks if misused.
Gordon LaboratoriesDec 10, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Clopidogrel Tablets, USP, 300 mg, 30 (5 x 6 unit-dose) count blister pack, Rx only, Manufactured by Dr. Reddy's
Dr. Reddy's recalls 300 mg Clopidogrel tablets due to failed dissolution testing at 18 months. Affected lots may not release medication properly.
Dr. Reddy'sDec 10, 2018 - Lower riskDrug
CBI Laboratories, Inc. recalls Advanced Protection Sunscreen spf 30 (Octinoxate 7.5%, Octisalate 5%, Oxybenzone 6%), 4.5 Oz/127.5 g tube.
CBI Laboratories recalls SPF 30 sunscreen with incorrect active ingredient percentages. Products may not provide intended protection. Consumers should contact the company for details.
CBI LaboratoriesDec 10, 2018 - Lower riskFood
Mylan Pharmaceuticals Inc. recalls DrNatura Toxinout Kit Broad Spectrum Detoxification Program
Mylan recalls DrNatura Toxinout Kit Broad Spectrum Detoxification Program due to undeclared soy allergen. Consumers should check lot numbers and contact Mylan for details.
MylanDec 10, 2018 - Use cautionMeat & poultry
3-D Meats, LLC Recalls Ready-To-Eat Beef Snack Stick Products due to Misbranding and Undeclared Allergens
USDA recalls 47 pounds of ready-to-eat beef snack sticks from 3-D Meats due to misbranding and undeclared milk allergen. Consumers urged not to consume and dispose of products.
3-D MeatsDec 9, 2018 - Use cautionVehicle
BMW X6 (2019) recall — Wheels
BMW is recalling certain 2018-2019 X6 models with potentially loose wheel bolts that could affect handling and increase crash risk. Owners should contact BMW for free bolt replacement.
BMWDec 9, 2018 - Use cautionMeat & poultry
Amboy Group, LLC Recalls Poultry Products due to Misbranding and Undeclared Allergens
USDA FSIS recalls Amboy Group poultry products due to undeclared milk, egg, and soy allergens. Consumers urged to discard products immediately.
Amboy GroupDec 7, 2018 - Stop using nowVehicle
DODGE CHALLENGER (2018) recall — Power Train
Chrysler recalls certain 2018 Dodge Challengers with Mopar Stage 1 kits due to cruise control defects. Check if your PCM part number is affected and get a free repair.
DodgeDec 7, 2018 - Use cautionVehicle
MINI CLUBMAN (2019) recall — Engine And Engine Cooling
BMW recalls certain 2019 MINI Clubman vehicles due to potential engine stall causing crash risk. Owners must contact BMW for free crankshaft sensor replacement.
BMWDec 7, 2018 - Use cautionMedical device
Ethicon Endo-Surgery Inc recalls PROXIMATE¿ PPH Hemorrhoidal Circular Stapler Product Code:PPH03 PPH03: The PROXIMATE¿ PPH Hemorrhoidal Circular Stapler
Ethicon recalls PROXIMATE PPH Hemorrhoidal Circular Staplers with specific product codes due to potential bleeding or soft tissue injury from improper assembly. Affected units include certain lot codes.
EthiconDec 7, 2018 - Lower riskMedical device
Spectranetics Corporation recalls Spectranetics AngioSculpt PTCA Scoring Balloon Catheter, balloon outer diameter 2.5mm, balloon length 15mm, REF
Spectranetics recalls AngioSculpt PTCA Scoring Balloon Catheter (2.5mm outer diameter) due to incorrect carton box used. Affected units may have packaging issues but no safety hazard is reported.
SpectraneticsDec 7, 2018 - Use cautionMedical device
Waldemar Link GmbH & Co. KG (Mfg Site) recalls LINK STEM with Microporous Surface MP Reconstruction Prosthesis, CEMENTLESS (Size XS-0, D: 12mm, L: 160mm), Reference
Waldemar Link recalls certain LINK STEM prosthesis models due to potential incorrect neck fit causing improper joint alignment. Affected units have specific lot numbers and sizes.
Waldemar LinkDec 7, 2018
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