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
34,959 found- Lower riskMedical device
SPINEART SA recalls Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures
SPINEART recalls JULIET Ti OL cage for orthopedic spinal procedures due to incorrect inner blister pack labeling. This mismatch may cause confusion in surgical use.
SPINEARTFeb 5, 2019 - Lower riskMedical device
Abbott Ireland Diagnostics Division recalls Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT Estradiol assay is a Chemiluminescent
Abbott recalls estradiol reagent kits that may show falsely high hormone levels for patients using mifepristone. Affected kits include specific lot numbers across multiple product lines.
AbbottFeb 5, 2019 - Stop using nowConsumer product
Fisher-Price Recalls Children's Power Wheels Barbie Campers Due to Injury Hazard
Fisher-Price recalls children's Power Wheels Barbie Dream Campers with model FRC29 due to risk of continuing to run after foot pedal release, posing injury hazard. Consumers must stop using and contact for repair.
Fisher-PriceFeb 5, 2019 - Stop using nowConsumer product
DeWALT Recalls Drills Due to Shock Hazard
DeWALT recalls DWD110 and DWD112 drills with date codes 2017-37-FY to 2018-22-FY due to shock hazard from wiring contacting moving parts. Consumers must stop using and get free repair.
DeWALTFeb 5, 2019 - Lower riskMeat & poultry
Q's American Best Trading Inc. Recalls Siluriformes Products Produced Without Benefit of Import Inspection
USDA FSIS recalls 1,008 pounds of imported Siluriformes fish from Vietnam that were not inspected before entering the US. Consumers urged not to consume these products.
Q'sFeb 4, 2019 - Use cautionVehicle
SPARTAN METROSTAR (2017) recall — Exterior Lighting
Precision is recalling 2017 Spartan Metrostar emergency vehicles with Whelen brake lights that may illuminate when brake pedal isn't pressed, risking crashes. Owners can get free replacement lights.
PrecisionFeb 4, 2019 - Use cautionVehicle
KME COMMERCIAL RESCUE (2017) recall — Latches/Locks/Linkages
KME is recalling certain 2017 Commercial Rescue and other models due to a risk of sliding cover falling unexpectedly, potentially causing injury. Owners should contact KME for free replacement of gas springs with improved locking.
KMEFeb 4, 2019 - Use cautionVehicle
LOTUS EVORA (2018) recall — Structure
Lotus recalls 2017-2018 Evora vehicles with stiff toe board that may cause knee injuries in crashes. Owners must have the toe board replaced free of charge by dealers.
LotusFeb 4, 2019 - Use cautionVehicle
JAYCO ALANTE (2019) recall — Electrical System
Jayco recalls 2014-2019 Alante motorhomes with missing 25amp fuse in blower circuit, which may overheat and cause fire. Owners must contact Jayco for free fuse installation.
JaycoFeb 4, 2019 - Use cautionVehicle
ENTEGRA VISION (2019) recall — Electrical System
Entegra is recalling certain 2019 Vision motorhomes built on Ford F53 chassis due to potential overheating wiring that could cause fire. Owners must have a 25amp fuse installed by dealers.
EntegraFeb 4, 2019 - Stop using nowMedical device
US Endoscopy Group Inc recalls US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock Clip is indicated for use in flexible
US Endoscopy recalls Padlock Clip defect closure system (Ref: C910001) due to potential esophageal laceration during patient procedures. Affected units include specific lot numbers listed in the recall notice.
US EndoscopyFeb 4, 2019 - Lower riskMedical device
CP Medical Inc recalls Plain and Chromic Gut Absorbable Surgical Sutures, sterile. 12 sutures per box. Product Usage: Plain Gut Sutures are
CP Medical recalls sterile Plain and Chromic Gut Absorbable Surgical Sutures (12 per box) after endotoxin tests showed potential sterility compromise. Affected lots include 822PG-HUF (170927-52, 180611-59), 822PG-DAR (171205-52), 810PG-1 (180924-51), and 822PG-1 (180924-53).
CP MedicalFeb 4, 2019 - Lower riskMedical device
Roche Diagnostics Corporation recalls Cobas¿ infinity central lab IT solution Material Number: 07154003001 Calculator/Data Processing Module, For Clinical Use
Roche recalls Cobas Infinity software versions 2.0-2.5 for potential QC alarm failures when switching bottles in clinical lab use. Affected units include specific serial numbers and material numbers.
RocheFeb 4, 2019 - Use cautionMedical device
Encore Medical, Lp recalls EMPOWR Locking Femoral Impactor , Part # 800-05-035, packaged in instrument tray FA EMP PAT TOOL KIT Part # 800-99-096
Encore Medical recalls EMPOWR Locking Femoral Impactor parts due to breakage risks and potential misalignment causing surgery delays or complications.
Encore MedicalFeb 4, 2019 - Use cautionMedical device
Moller Vital recalls Molift 2-Point sling bar, an accessory for Molift Mover 180/Air. Item nos. 1830001 1830002 1830002C 1830003
Moller Vital recalls Molift 2-Point sling bars (item nos. 1830001-1830003) made between May 2013 and October 2018 due to hook breakage causing patient falls. Affected users should check their product labels.
Moller VitalFeb 4, 2019 - UnratedDrug
ICU Medical Inc recalls 0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC
ICU Medical recalls 0.9% Sodium Chloride Injection, USP 1000 mL flexible container due to CGMP deviations. This product is for prescription use only and may be unsafe for medical administration.
ICU MedicalFeb 4, 2019 - UnratedDrug
Akorn Inc recalls Moisturizing Lubricant Eye Drops, 0.25% Sodium Carboxymethylcellulose, 0.5 Fl OZ (15mL) Distributed by: Walgreen Co,
Akorn recalls moisturizing eye drops due to stability issues. Products may have failed sodium perborate tests. Check NDC 00363-9651-01 and lot numbers for affected items.
AkornFeb 4, 2019 - Lower riskFood
Frito-Lay, Inc. recalls Stacy's Simply Naked Pita Chips 7 1/3 ounce bags
Frito-Lay recalls Stacy's Simply Naked Pita Chips 7 1/3 oz bags due to potential undeclared milk. Check for use-by date 04/23/2019 and manufacturing code 65M127902.
Frito-LayFeb 4, 2019 - Lower riskFood
Jacques Torres Manufacturing , llc. recalls Jacques Big Daddy Dark Chocolate Bar. The product comes in un-coded 2.2 lbs. (1kg) clear plastic package overwrapped
Jacques Torres recalls Big Daddy Dark Chocolate Bar due to undeclared milk content. Consumers should check for un-coded 2.2 lb clear plastic packages. No remedy specified in recall notice.
Jacques TorresFeb 4, 2019 - Use cautionMeat & poultry
Taylor Farms TX, Inc. Recalls Chicken Products Due To Misbranding And Undeclared Allergens
USDA FSIS recalls 2,100 pounds of Taylor Farms chicken products mislabeled as Chile Relleno with undeclared wheat allergen. Consumers urged not to consume or discard items.
Taylor FarmsFeb 2, 2019 - Stop using nowMeat & poultry
Pilgrim's Pride Corporation Recalls Breaded Popcorn Chicken Products Due To Possible Foreign Matter Contamination
Pilgrim's Pride recalls ~58,020 lbs of frozen popcorn chicken due to possible rubber contamination. Check your freezer for affected lots and do not eat.
Pilgrim's PrideFeb 1, 2019 - Use cautionVehicle
PIERCE ARROW XT (2016) recall — Electrical System
Pierce is recalling 2016 Arrow XT aerial vehicles due to risk of ladder moving unexpectedly, potentially causing injury. Owners should contact Pierce customer service for free reprogramming.
PierceFeb 1, 2019 - Use cautionVehicle
FORD ECOSPORT (2019) recall — Seats
Ford is recalling 2019 EcoSport vehicles with improperly welded front seat frames that may not stay secure in crashes. Owners must have seat assemblies replaced free by dealers.
FordFeb 1, 2019 - Use cautionMedical device
Cook Inc. recalls Cook Transseptal Needle, Reference Number TSNC-18-71.0, Order Number G02364. For transseptal left heart access in both
Cook recalls transseptal needles with missing back bevel that could damage heart introducer during procedure. Affected models include TSNC-18-71.0 (Order G02364).
CookFeb 1, 2019 - Lower riskMedical device
Zimmer Trabecular Metal Technology, Inc. recalls NexGenTrabecular Metal Tibial Half Block Augment, Left Lateral/Right Medial, Size 4 5MM Thickness W/Screws Item Number:
Zimmer recalls specific NexGen Tibial Half Block Augments due to potential mismatch between product in box and label. Affected items have unique lot numbers; consumers should verify their product details.
ZimmerFeb 1, 2019 - Lower riskMedical device
Becton Dickinson & Company recalls 3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573
Becton Dickinson recalls 3mL Luer-Lok Syringes with incorrect scale markings that may lead to inaccurate dosing. Affected units include Catalog Number 309657, UDI 30382903096573, and Lot Number 8303571.
Becton DickinsonFeb 1, 2019 - Lower riskMedical device
Physio-Control Inc recalls LIFEPAK 15 Monitor/Defibrillator Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) is a complete acute
Physio-Control
Physio-ControlFeb 1, 2019 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Moxifloxacin Ophthalmic Solution USP, 0.5%, 3 mL dropper bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc.
Lupin Pharmaceuticals recalls 0.5% moxifloxacin eye drops due to impurities detected in stability testing. Affected lots from 2019-2020 may cause eye injury if used.
Lupin PharmaceuticalsFeb 1, 2019 - UnratedDrug
Mylan Institutional Inc recalls Levoleucovorin Injection, 250 mg/25 mL, (10 mg/mL), 25 mL Single-Use Vial, Rx only, Manufactured for: Mylan
Mylan recalls 250 mg/25 mL Levoleucovorin Injection vials due to copper salts causing particulate matter. Affected vials have NDC 67457-601-30, lots APB032/033, expiring April 2019.
MylanFeb 1, 2019 - Use cautionDrug
Mylan Pharmaceuticals Inc. recalls Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray, 137 mcg/50 mcg per spray, 120 Metered
Mylan recalls Dymista nasal spray due to potential broken glass in bottle necks. Stop using if you have this product.
MylanFeb 1, 2019
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