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
34,896 found- Use cautionMedical device
Siemens Medical Solutions USA, Inc. recalls Biograph mCT Systems: (a) Biograph mCT S(64)-3R, Material Number 10248669 Product Usage: The Siemens Biograph mCT and
Siemens recalls Biograph mCT and Biograph mCT Flow systems due to potential laser cover windows falling off. Affected models include S(64)-3R, S(40)-4R, and others with specific material numbers and serial numbers.
SiemensMay 29, 2018 - Lower riskMedical device
Implant Direct Sybron Manufacturing, LLC recalls Implant Direct Legacy Implant Closed-Tray Transfer-Concave Profile, 3.5mmD Platform. Dental implant component, used
Implant Direct recalls dental implants with potentially mislabeled caps. Correct part number on main vial label. No immediate action needed.
Implant DirectMay 29, 2018 - Use cautionMedical device
Zeiss, Carl Inc recalls Disinfection unit UV (432332-9020-000) for the Celldiscoverer 7 microscope
Zeiss recalls the Celldiscoverer 7 microscope's UV disinfection unit (432332-9020-000) due to potential UV radiation exposure if the unit activates outside the housing.
ZeissMay 29, 2018 - Lower riskDrug
Pharmaceutical Associates Inc recalls Nystatin Oral Suspension, USP, 500,000 units/5 mL, For Institutional Use Only, packaged in 5 mL cups, Rx Only,
Pharmaceutical Associates recalls Nystatin Oral Suspension (500,000 units/5mL) for resuspension problems. This product is for institutional use only and requires a prescription.
Pharmaceutical AssociatesMay 29, 2018 - Stop using nowFood
Morley Candy Makers, Inc. recalls Milk Chocolate Covered Fudge Bites, 3.75oz, PET Pouch, 12 packages per case
Morley Candy Makers recalls Sanders Milk Chocolate Covered Fudge Bites due to undeclared almonds. Check your lot code and best-by date.
SandersMay 29, 2018 - Lower riskFood
Newly Weds Foods Inc recalls Commercial breaders and batters Product B58042 Breader XI- 50 pound bags Product B58915 Breader X1- 40 pound bags
Newly Weds Foods recalls 50-pound and 40-pound breaders and batters due to foreign plastic material. Consumers should stop using affected products to avoid potential injury.
Newly Weds FoodsMay 29, 2018 - Lower riskFood
Shearers Foods, Llc recalls Meijer DILL PICKLE FLAVORED CLASSIC CRUNCH POTATO CHIPS***UPC 719283594365***LOT CODE***
Shearers Foods recalls Dill Pickle Flavored Classic Crunch Potato Chips due to milk allergen not declared on labeling. Consumers should check UPC 719283594365 and lot codes for affected products.
Shearers FoodsMay 29, 2018 - Lower riskMedical device
QIAGEN recalls EZ1 DSP Virus Kit (48), IVD, REF 62724 intended for in vitro diagnostic use.
QIAGEN recalls EZ1 DSP Virus Kit (48) for potential incorrect test results from underfilled reagent wells. Affected units have specific UDI and lot numbers.
QIAGENMay 28, 2018 - Stop using nowFood
Trader Joes Company recalls Trader Joe's Artisan Bread - Organic French Baguette; (Brown and Serve) Keep frozen; Product code 53835; 24 x 11.5 oz.
Trader Joe's recalls 24-pack of Organic French Baguette (Product Code 53835) due to potential Listeria monocytogenes contamination. Consumers should discard frozen items immediately.
Trader Joe'sMay 28, 2018 - Use cautionVehicle
CHEVROLET SONIC (2018) recall — Seats
GM recalls 2018 Chevrolet Sonic vehicles with potentially weak driver seat-backs that could fail in rear crashes, increasing injury risk. Owners must have seat replaced free by dealers.
ChevroletMay 27, 2018 - Use cautionMeat & poultry
Hormel Foods Corporation Recalls Canned Pork and Chicken Products due to Possible Foreign Matter Contamination
USDA FSIS recalls Hormel canned pork and chicken products from Feb 2018 due to possible metal contamination. Consumers urged not to consume; products should be thrown away or returned.
HormelMay 26, 2018 - Use cautionVehicle
MASERATI GHIBLI (2018) recall — Structure
Maserati is recalling 2018 Ghibli vehicles with incomplete front sub frame welds that could cause loss of vehicle control and crash risk. Owners must have sub frame inspected and repaired free of charge.
MaseratiMay 25, 2018 - Use cautionVehicle
JEEP WRANGLER (2018) recall — Steering
Chrysler recalls 2018 Jeep Wrangler vehicles with potentially split steering welds that could cause loss of steering responsiveness and crash risk. Owners must have steering shaft inspected and repaired free of charge.
ChryslerMay 25, 2018 - Use cautionVehicle
TIFFIN BREEZE (2019) recall — Structure
Tiffin recalls 2018-2019 Breeze motorhomes with door that may open while moving, risking injury. Owners must contact Tiffin for free door lock fix.
TiffinMay 25, 2018 - Use cautionVehicle
JEEP CHEROKEE (2019) recall — Engine And Engine Cooling
Chrysler recalls certain 2019 Jeep Cherokees with 2.0L engines due to missing valve stem keepers or reversed camshaft caps that can cause engine damage or camshaft failure, increasing crash risk. Owners will receive free repairs.
ChryslerMay 25, 2018 - Lower riskMedical device
Radiometer America Inc recalls ABL90 FLEX analyzers with software versions 3.3MR1 or below. The ABL90 FLEX Analyzer is a portable, automated Analyzer
Radiometer recalls ABL90 FLEX analyzers with software versions 3.3MR1 or below due to potential incorrect test results from aspirating Cal 2 solution instead of rinse solution during specific use patterns.
RadiometerMay 25, 2018 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls AXIOM Artis with Laird Cooling Unit for SSFD: Material # 7555118. Artis is an angiography system developed for single
Siemens recalls AXIOM Artis angiography systems with Laird Cooling Unit (Material #7555118) due to defective sealing causing coolant to enter electrical parts, potentially causing sudden shutdowns during procedures.
SiemensMay 25, 2018 - Lower riskMedical device
GE Healthcare Finland Oy recalls GE Healthcare CARESCAPE Monitor B650
GE Healthcare recalls 142 CARESCAPE Monitor B650 units with serial numbers starting with SEW or SK. When multiple units connect to the same network and experience prolonged overload, they may restart repeatedly without completing the process. No immediate action is required for users but should monitor network stability.
GE HealthcareMay 25, 2018 - Lower riskMedical device
Medtronic Neuromodulation recalls Vectris(TM) Trial Screening Lead Kit for Spinal Cord Stimulation, Models: (a) 977D160 (b) 977D260 Product Usage: The
Medtronic recalls Vectris Trial Screening Lead Kits (models 977D160 and 977D260) due to a potential manufacturing defect in the curved tip introducer needle that may cause difficulty advancing or withdrawing the lead during spinal cord stimulation implantation.
MedtronicMay 25, 2018 - UnratedDrug
Jubilant Cadista Pharmaceuticals, Inc. recalls Valsartan Tablets USP, 320 mg, 90 tablet, Rx Only, Manufactured by: Jubilant Generics Ltd. Roorkee - 247661, India,
Jubilant Cadista recalls 320mg Valsartan tablets with incorrect excipient (Crospovidone) that may cause serious health issues. Affected lots: VR417065A, VR417066A (expiring 10/2019).
Jubilant CadistaMay 25, 2018 - Lower riskDrug
Shadow Holdings DBA Bocchi Labs recalls X-Jow (menthol USP) Pain Gel, 1.25%, packaged in a) 4 oz. (113g) bottles (UPC 850547 00502 6) and b) 8 oz. (226g)
Bocchi Labs recalls X-Jow (menthol USP) Pain Gel 1.25% due to potential bacterial contamination. Affected products include 4oz and 8oz bottles with specific UPCs. Consumers should check their products and contact the manufacturer for details.
Bocchi LabsMay 25, 2018 - Stop using nowFood
Global Commodities Inc recalls WATAN DRY FRUITS PREMIUM QUALITY NATURAL DRIED APRICOT WITH PITT, NET WT. 1 LB, and 0.50 LB, PRODUCE OF PAKISTAN,
Global Commodities Inc recalls Watan dried apricots due to undeclared sulfites. Check your pantry for affected lots from Pakistan.
WatanMay 25, 2018 - Use cautionFood
Dean Foods, Inc. recalls Baskin Robbins Mint Chocolate Chip
Dean Foods recalls Baskin Robbins Mint Chocolate Chip ice cream due to unlabeled coconut. Check lot code 14 MAR 19.
Baskin RobbinsMay 25, 2018 - Use cautionFood
Yukon Jackson recalls Coffee Toffee - 4 oz. packages. UPC 6 55974 89001 2. The label is read in parts: "***Ingredients: butter (milk), sugar,
Yukon Jackson recalls 24 packages of 4 oz. Coffee Toffee due to undeclared pecans, posing a risk to those with nut allergies.
Yukon JacksonMay 25, 2018 - Use cautionVehicle
GMC TERRAIN (2018) recall — Air Bags
GM recalls 2018 GMC Terrain vehicles with faulty airbag system that may not deploy during crashes. Owners must have SDM reprogrammed by dealers.
GMCMay 24, 2018 - Use cautionVehicle
FORD MUSTANG (2018) recall — Engine And Engine Cooling
Roush is recalling certain 2018 Mustang supercharger kits (part R1318-6006P1-AA) due to potential fuel leaks causing fire risk. Owners must contact Roush for free replacement of defective fuel rail subassemblies.
RoushMay 24, 2018 - Lower riskMedical device
Fort Defiance Industries, LLC recalls FDI FORT DEFIANCE INDUSTRIES P2131 AUTOMATED FIELD STEAM STERILIZER, NSN: 6530-01-641-4641 Product Usage: The Fort
Fort Defiance recalls P2131 sterilizers due to water deposits from long-term storage causing potential issues with rear sight gauge or water level switch. Affected units have serial numbers AFS-0001 to AFS-0199.
Fort DefianceMay 24, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The
Zimmer Biomet recalls Vanguard Complete Knee Systems with specific model numbers due to potential mix-up of 12mm and 14mm tibial bearings, which could lead to extended surgery time.
Zimmer BiometMay 24, 2018 - Stop using nowMedical device
Draeger Medical, Inc. recalls Perseus A500 Anesthesia Machine; Cat. no. MK06000 Product V Product Usage: Intended for use in anesthetizing adults,
Draeger Medical recalls Perseus A500 anesthesia machines due to potential risk of delivering 100% nitrous oxide, which could cause patient hypoxia and death. Affected units have specific model numbers and were sold for medical use.
DraegerMay 24, 2018 - Use cautionMedical device
GE Healthcare, LLC recalls Discovery NM/CT 670 DR, model 5376204-70-56 intended for use in detecting, localizing, diagnosing of diseases and organ
GE Healthcare recalls Discovery NM/CT 670 DR model 5376204-70-56 due to potential electric hazard from incorrect wiring during installation. Affected units may not shut off all power, risking electric shock. Contact GE for remedy.
GE HealthcareMay 24, 2018
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