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
35,006 found- UnratedDrug
Lupin Pharmaceuticals Inc. recalls Metformin Hydrochloride Extended-release Tablets USP, 500 mg, 60 count bottle, Rx only, Manufactured for Lupin
Lupin Pharmaceuticals recalls 500mg extended-release metformin tablets due to NDMA impurity exceeding safe levels. Affected batches manufactured in India with specific batch numbers.
LupinJun 11, 2020 - Stop using nowFood
Rong Shing Trading NY Inc recalls Xi Zhi Liang Fruit Jelly Cups; 21.1oz (600g); packaged in pink, yellow, and blue plastic backpacks with numerous
Rong Shing Trading recalls Xi Zhi Liang Fruit Jelly Cups due to a significant choking hazard. Check your backpacks for pink, yellow, or blue packaging.
Xi Zhi LiangJun 11, 2020 - Lower riskFood
GOLDEN NUTRITION INC recalls Anti-Viral Immune Enhance "Corona Virus (COVID-19) " "Influenza (H1N1)" "Bronchitis" "Common Cold" 60 Capsules, Dietary
Golden Nutrition recalls 60-capsule immune supplements with drug claims for COVID-19, influenza, and colds. Products sold with specific lot numbers and expiration dates.
Golden NutritionJun 11, 2020 - Lower riskFood
Abbott Nutrition, Division of Abbott Laboratories recalls Similac Pro-Advance Infant Formula with Iron, Milk-Based, Ready to Feed, 32 FL OZ (1 QT)
Abbott Nutrition recalls Similac Pro-Advance infant formula bottles that were filled with water instead of formula. These bottles were not intended for sale and pose a risk of improper feeding.
Abbott NutritionJun 11, 2020 - Use cautionConsumer product
Davina Wellness Recalls Wintergreen Essential Oil and Essential Oil Blend with Wintergreen Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
Davina Wellness recalls wintergreen essential oil and sore muscle blend products due to non-child-resistant packaging, posing poisoning risk to young children. Consumers should store out of reach and contact for free child-resistant caps.
Davina WellnessJun 11, 2020 - Stop using nowConsumer product
Bonnsu Recalls Miniware Teething Spoons Due to Choking Hazard
Bonnsu recalls Miniware teething spoons due to choking hazard in infants. The product can break in mouth during use, posing serious risk. Consumers should stop using immediately and get free replacement.
BonnsuJun 11, 2020 - Use cautionVehicle
FLEETWOOD BOUNDER (2020) recall — Equipment
REV recalls 2020 Fleetwood Bounder motorhomes with specific Dometic propane stoves due to potential gas leaks causing fire. Owners must contact REV for free repairs.
REVJun 10, 2020 - Use cautionMedical device
Elekta Instrument AB recalls Leksell Vantage Stereotactic System, UDI/GTIN 7340048304887
Elekta recalls specific Leksell Vantage Stereotactic System models due to potential improper locking mechanism function at the Instrument Carrier and Arc interface.
ElektaJun 10, 2020 - Use cautionMedical device
NuVasive Inc recalls Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended
NuVasive recalls NVM5 EMG Module (REF 8020015) due to incorrect component causing potential delay in spinal surgery monitoring. Affected units have specific model and lot numbers.
NuVasiveJun 10, 2020 - Lower riskMedical device
Intuitive Surgical, Inc. recalls Ion Catheter Reprocessing Cover, IF1000 (Part Number:490114-02) UDI:00886874116845.
Intuitive Surgical recalls Ion Catheter Reprocessing Cover model IF1000 (Part 490114-02) due to potential cleaning chemical retention during reprocessing, which may cause system failure.
Intuitive SurgicalJun 10, 2020 - Lower riskMedical device
Ethicon, Inc. recalls PERMA-HAND/MERSILK SILK BLU and VIRGIN SILK BLU, Product Codes EH7457G EH7983G FV768 FV769 FV7771 U7058 U7059 W1782
Ethicon recalls Perma-Hand and Virgin Silk Blue sutures with product codes EH7457G and others due to potential shelf life issues beyond 5 years.
EthiconJun 10, 2020 - Lower riskDrug
Alembic Pharmaceuticals Limited recalls Aripiprazole Tablets, USP, 2 mg, 30 Tablets per bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited
Alembic Pharmaceuticals recalls 2mg aripiprazole tablets due to label mix-up with 5mg tablets. This could lead to incorrect dosing if taken without proper label check.
Alembic PharmaceuticalsJun 10, 2020 - Lower riskDrug
Crown Laboratories recalls Nystatin Cream, USP 100,000 units per gram, 30 grams, Rx Only, Manufactured and Distributed by: Crown Laboratories,
Crown Laboratories recalls Nystatin Cream, USP 100,000 units per gram, 30 grams (Rx Only) due to subpotent drug levels. This may not treat infections effectively.
Crown LaboratoriesJun 10, 2020 - Lower riskDrug
American Health Packaging recalls Nabumetone Tablets, USP, 500 mg, 100 Tablets per carton (10 tablets x 10 blister cards), Rx only, Distributed by:
American Health Packaging recalls 500mg Nabumetone Tablets due to missing Medication Guide label on carton. This affects prescription-only products sold from 2020 to 2021. Consumers should check labels for NDC 60687-374-01.
American Health PackagingJun 10, 2020 - Stop using nowConsumer product
Ushio America Recalls Indiglow LED T8 Lamps Due to Injury Hazard
Ushio America recalls Indiglow LED T8 lamps that can overheat, causing glass tubes to fall and strike nearby people. Consumers should stop using and get a refund or replacement.
Ushio AmericaJun 10, 2020 - Stop using nowConsumer product
Island Wear Recalls Strollers Due to Violation of Federal Stroller and Carriage Safety Standard; Fall and Choking Hazards
Island Wear recalls umbrella strollers with a gap in the restraint system that can cause falls and detachable grab bar foam that poses choking risks. Consumers must stop using and get a refund.
Island WearJun 10, 2020 - Stop using nowConsumer product
DICK'S Sporting Goods Recalls Safety Ropes Due to Fall and Injury Hazards
DICK'S Sporting Goods recalls safety ropes that can fail in freezing conditions, causing falls and injuries. Return to store for refund or credit.
DICK'S Sporting GoodsJun 10, 2020 - Lower riskMedical device
Bausch & Lomb Surgical, Inc. recalls enVista one-piece hydrophobic acrylic toric intraocular lens, Bausch and Lomb - Product Usage: is indicated for primary
Bausch & Lomb recalls enVista one-piece hydrophobic acrylic toric intraocular lenses with misaligned toric axis marks that could affect surgical outcomes after cataract removal.
Bausch & LombJun 9, 2020 - Lower riskMedical device
EHOB, Inc. recalls Expansion Control Overlay, Item No. 1004EC - Product Usage: The EHOB WAFFLE Overlay is more than a support surface,
EHOB recalls WAFFLE Overlay (Item 1004EC) due to potential blood contamination in some lots. This may pose a risk of infection. Affected units were sold in specific hospital lots.
EHOBJun 9, 2020 - UnratedDrug
MasterPharm LLC recalls Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle, This is a compounded drug not for resale,
MasterPharm recalls compounded minoxididil/biotin/spironolactone capsules due to elevated drug levels. This compounded drug (not for resale) may pose risks from high minoxidil content. Consumers should contact the manufacturer for details.
MasterPharmJun 9, 2020 - Stop using nowVehicle
CHEVROLET CORVETTE (2020) recall — Latches/Locks/Linkages
GM recalls 2020 Corvettes because the front trunk release button may fail after 10 minutes, trapping occupants. Free software update available.
ChevroletJun 8, 2020 - Use cautionMedical device
Philips North America, LLC recalls Philips M3015A Microstream CO2 Extension Model No. 862393 -used with an lntelliVue X3 Patient Monitor (Model No.
Philips recalls M3015A Microstream CO2 Extension Model 862393 used with X3 Patient Monitor (Model 867030) or MMX server (Model 867036) due to communication disruption risk.
PhilipsJun 8, 2020 - Use cautionMedical device
KCI USA, INC. recalls ACTIV.A.C Therapy System; Model Numbers; US: 340000 ACTIV.A.C., NORTH AMERICAN UDI (01)00878237008188 - Product Usage:
KCI recalls ACTIV.A.C Therapy System models from 2007-2020 with software up to 3.11 due to risk of stopping negative pressure wound therapy without user notification.
KCIJun 8, 2020 - Use cautionMedical device
Hocoma AG recalls Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD ; 30004 LokomatPro L6.2 120V Kombi; 30005 LokomatPro L6.2
Hocoma recalls Lokomat Pro devices with specific catalog numbers due to potential uncontrolled movement of the Body Weights Support Rope, which could cause injury during therapy sessions.
HocomaJun 8, 2020 - Lower riskMedical device
Medtronic Sofamor Danek USA Inc recalls Accurian RF Ablation, Cannula pk, Accurian, 150mm, 20G, 10mm, CS Product Number: AC0012 GTIN / UPN: 20763000153629 -
Medtronic Sofamor Danek recalls Accurian RF Ablation Cannula due to insertion difficulty caused by probe catching on cannula hub lip. Affected units have specific product numbers and lot numbers.
Medtronic Sofamor DanekJun 8, 2020 - Lower riskMedical device
New Standard Device Inc recalls 1.8mm Truss Wire, REF: 900217, a Component of Metalogix Revolution External Plating System
New Standard Device recalls 1.8mm truss wire (REF: 900217) used in Metalogix Revolution External Plating System. This component is being replaced with stronger 2.0mm wires to reduce breakage.
New Standard DeviceJun 8, 2020 - Lower riskMedical device
HF Acquisition Co. LLC recalls STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: is intended to prepare physicians with advanced
HealthFirst recalls STAT KIT Z-1000 emergency medical kits due to missing hand suction pump. This could impair emergency response during cardiac events. Affected kits have part numbers 1003550 and 1004330.
HealthFirstJun 5, 2020 - Lower riskMedical device
Richard Wolf GmbH recalls Tube Set for TEM - Product Usage: Transanal Endoscopic Microsurgery (TEM) combination system and the instrument set for
Richard Wolf recalls TEM Tube Sets with small diameter tube material that may cause improper use during transanal endoscopic procedures. Affected units include Lot 32324159, Model 4170.801.
Richard WolfJun 5, 2020 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls ADVIA Chemistry Calibrator
Siemens Healthcare recalls ADVIA Chemistry Calibrator lots 534177 and 960742 due to calibration errors affecting bilirubin test accuracy. Affected users should contact Siemens for details.
Siemens HealthcareJun 5, 2020 - Use cautionMedical device
Verathon, Inc. recalls GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Video Laryngoscope System Per
Verathon recalls GlideScope Core OneTouch Smart Cable (REF 0800 0601) due to potential video disruption during intubation, risking critical patient delays. Affected users should check serial numbers and contact Verathon for details.
VerathonJun 5, 2020
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