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
35,025 found- Lower riskMedical device
Edwards Lifesciences, LLC recalls Edwards PediaSat Oximetry Catheter Set, REF: XT3515SJ, Exterior Diameter 5.5F, Usable Length 15 cm, Number of Lumens:
Edwards Lifesciences recalls PediaSat Oximetry Catheter Sets with potential internal leaks. Affected units have specific model and lot numbers. Contact for return instructions.
Edwards LifesciencesJul 9, 2021 - Lower riskMedical device
Medtronic Neuromodulation recalls Medtronic Vectris SureScan MRI, Catalog Numbers: a) 977A260 b) 977A275 c) 977A290
Medtronic recalls Vectris SureScan MRI devices with specific catalog numbers due to incorrect lead electrode spacing information on packaging. This could lead to improper use during MRI procedures.
MedtronicJul 9, 2021 - UnratedMedical device
Ortho8, Inc. recalls CIRCUL8 LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF: 08-0020, Rx Prescription Only,
Ortho8 recalls CIRCUL8 LUXE DVT prevention devices sold without FDA clearance. This prescription-only device may pose risks due to lack of regulatory approval.
Ortho8Jul 9, 2021 - UnratedDrug
Innoveix Pharmaceuticals Inc recalls Compounded Lyophilized Semorelin/Ipamorelin 3 mg For subcutaneous or intramuscular injection, Rx Only, Compounded by:
Innoveix Pharmaceuticals recalls compounded semorelin/ipamorelin 3mg injections due to lack of sterility assurance. This could lead to infections if used improperly. Affected lots expired by January 2022.
InnoveixJul 9, 2021 - UnratedFood
Bountiful Trading Inc recalls Kroger brand, Vitamin D3 125 mcg softgels, 100 count, Green HDPE packaging
Kroger recalls Vitamin D3 softgels (125 mcg, 100 count) due to potential Coq10 contamination. Check packaging for green HDPE and lot numbers to determine if affected.
KrogerJul 9, 2021 - UnratedMedical device
Carl Zeiss Meditec, Inc. recalls Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX - "CIRRUS HD-OCT Model 6000"
Carl Zeiss Meditec recalls Cirrus HD-OCT Model 6000 devices that were sold without proper pre-market clearance for high resolution tomographic imaging. Affected units have specific serial numbers listed in the recall notice.
Carl Zeiss MeditecJul 8, 2021 - Stop using nowMedical device
Sunrise Medical (US) LLC recalls Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of
Sunrise Medical recalls Zippie Voyage strollers with model EIZ16/EIZ18 that may detach unexpectedly, causing injury. Affected units include specific serial ranges. Stop using immediately to prevent falls.
Sunrise MedicalJul 8, 2021 - Lower riskMedical device
Vascutek, Ltd. recalls The Instructions for Use (IFU) for: Gelsoft Plus Bifurcate, Gelsoft Plus Ax-Fem, GelsoftPlus ERS Ax-Fem, Gelweave
Vascutek recalls certain Gelsoft vascular grafts due to incorrect Instructions for Use distribution to international consignees instead of U.S. consignees. No action required for users.
VascutekJul 8, 2021 - Use cautionMedical device
Argon Medical Devices, Inc recalls Scorpion Portal Vein Access Set - Product Usage: used to gain access to the hepatic vein and guide a sharp puncture
Argon Medical recalls Scorpion Portal Vein Access Sets with sheaths that crack at tips, posing a risk of injury during liver vein procedures. Affected items include specific stylets and needles sold with lot number 11369609.
Argon Medical DevicesJul 8, 2021 - Stop using nowConsumer product
LoHi Tech Recalls SOWTECH Espresso Machines Due to Burn Hazard (Recall Alert)
LoHi Tech recalls SOWTECH espresso machines with glass carafes due to breakage risk causing burns. Affected models CM6811 sold with glass carafe need immediate replacement with metal carafe.
LoHi TechJul 8, 2021 - Stop using nowConsumer product
ECHO EGi-2300 Watt Generators Recalled Due to Fire and Burn Hazards; Manufactured by TTI (Recall Alert)
ECHO EGi-2300 Watt Generators with specific serial numbers recalled due to overheating risks. Consumers must stop using and contact ECHO for free repair.
ECHOJul 8, 2021 - Stop using nowConsumer product
Canyon Furniture Recalls Creekside Children's Chests of Drawers Due to Tip-Over and Entrapment Hazards; Sold Exclusively at Rooms To Go (Recall Alert)
Canyon Furniture recalls Creekside Kids Five-Drawer Chests sold at Rooms To Go due to tip-over and entrapment risks for children. Unanchored chests may cause serious injury or death.
Canyon FurnitureJul 8, 2021 - Lower riskMedical device
Baxter Healthcare Corporation recalls Dose IQ Safety Software used with Spectrum IQ Infusion Pump
Baxter recalls Dose IQ Safety Software (version 9.0.x) for Spectrum IQ pumps due to drug identifier mismatch risk. Affected users should contact Baxter for remedy.
Baxter HealthcareJul 7, 2021 - Lower riskDrug
LNK International, Inc. recalls Acetaminophen EXTRA STRENGTH Pain Reliever / Fever Reducer, Enteric Coated, 50 Coated Tablets/ 500 mg each, Distributed
LNK International recalls 500mg acetaminophen tablets labeled as enteric coated but not actually coated due to labeling error. Consumers should check product details and contact the manufacturer for guidance.
LNK InternationalJul 7, 2021 - UnratedDrug
Aurobindo Pharma USA Inc. recalls Sulfamethoxazole and Trimethoprim Tablets, USP, 800mg/160mg Double Strength, 500 Tablets, Rx Only, Distributed by:
Aurobindo Pharma recalls 500-tablet sulfamethoxazole-trimethoprim (800mg/160mg) prescription medication due to potential metal contamination. This recall affects specific batches made in India with NDC 65862-420-05.
Aurobindo PharmaJul 7, 2021 - Stop using nowConsumer product
One Twenty Clothing Company Recalls "Sovereign Athletic" Children's Robes Due to Violation of Federal Flammability Standard and Burn Hazard
One Twenty Clothing recalls Sovereign Athletic children's robes that fail federal flammability standards, risking burn injuries. Consumers must stop using and return for full refund.
One Twenty ClothingJul 7, 2021 - Use cautionVehicle
HONDA ODYSSEY (2022) recall — Seats
Honda recalls 2022 Odyssey vehicles with second-row outboard seats that may not lock properly, increasing injury risk. Owners must have seats replaced free by dealers.
HondaJul 6, 2021 - Lower riskMedical device
Advance Dx, Inc. recalls Advance Dx 100 Blood Collection Card Quantity 25 REF CMT01 Advance Dx 100 Blood Collection Card and Foil Bags Quantity
Advance Dx recalls 25-count blood collection cards and 500-pack foil bags due to high glucose test results. Consumers should check product details and contact the company for remedy.
Advance DxJul 6, 2021 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc recalls Atellica IM BR 27.29 (BR) Assay 250 Test Kit- in vitro diagnostic use in the quantitative serial determination of
Siemens Healthcare recalls Atellica IM BR 27.29 Assay 250 Test Kits due to incorrect calibration interval in instructions. Kits may give inaccurate cancer antigen CA 27.29 results if used beyond 3-day calibration.
Siemens HealthcareJul 6, 2021 - Stop using nowFood
5000 Years Foods, Inc. recalls 5000 Years Foods NO MSG SLICED CABBAGE KIMCHI in 5GAL plastic tubs, and 128 oz, 64 oz, 32 oz, & 16 oz glass jars
5000 Years Foods recalls No MSG Sliced Cabbage Kimchi in plastic tubs and glass jars due to potential Listeria monocytogenes contamination.
5000 Years FoodsJul 6, 2021 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER HDX (2019) recall — Fuel System, Diesel
Daimler Trucks North America recalls 2018-2021 Thomas Built Buses Saf-T-Liner HDX school buses with potential fuel leaks that could cause fire if ignition sources are present.
Thomas Built BusesJul 5, 2021 - Use cautionVehicle
AIRSTREAM GLOBETROTTER (2021) recall — Equipment
Airstream is recalling certain 2020-2021 Globetrotter travel trailers due to adhesive failure on cabinet doors that could separate and fall, risking injury to occupants.
AirstreamJul 5, 2021 - Use cautionVehicle
FCCC XC CHASSIS (2020) recall — Fuel System, Diesel
DTNA recalls certain Freightliner and Western Star diesel chassis trucks (2018-2021) due to a fuel leak that increases fire risk. Dealers will replace parts free of charge.
Freightliner / Western StarJul 5, 2021 - Use cautionMedical device
Zeltiq Aesthetics, Inc recalls CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1, SW release 3.0.2
Zeltiq Aesthetics recalls CoolSculpting Elite System software versions 2.0 through 3.0.2 due to potential error messaging that could cause users to re-treat areas within 24 hours or miss thermal events.
Zeltiq AestheticsJul 5, 2021 - Stop using nowFood
LSG SKY CHEFS recalls Circle K Chicken Salad Sandwich, 5.9 oz. (167g) clamshell packaging with tamper strip, UPC 815138013996, Manufactured
Circle K recalls chicken salad sandwiches due to potential Listeria monocytogenes contamination. Check your best buy dates and UPC.
Circle KJul 5, 2021 - Use cautionVehicle
UTILITY TRAILER VS2DC (2017) recall — Structure
Utility Trailer is recalling 2017 VS2DC trailers with a missing weld that could cause slider rail detachment and crash risk. Owners notified via mail; free repair available.
Utility TrailerJul 4, 2021 - Stop using nowMeat & poultry
Tyson Foods Inc. Recalls Ready-To-Eat Chicken Products Due to Possible Listeria Contamination
Tyson recalls ~8.9M lbs of ready-to-eat chicken due to possible Listeria contamination. Check labels and discard or return immediately.
Tyson FoodsJul 3, 2021 - Use cautionMedical device
Laboratoires Bodycad, Inc. recalls Torque Limiting Adaptor, AO Connect, 4 N-m, part #027-203, reusable, a component of the Bodycad Fine Osteotomy Implant
Bodycad recalls specific torque limiting adaptors and osteotomy trays due to breakage risk when used counterclockwise or with power tools. Affected items include part #027-203 and specific lot numbers.
BodycadJul 2, 2021 - Lower riskMedical device
Hero Health recalls The Hero Model 100 (H-100) is a system consisting of a smart pill dispenser and a medication management app.
Hero Health recalls Model 100 (H-100) smart pill dispensers due to a prompt for missed doses after dispensing. Affected users should contact Hero Health for details.
Hero HealthJul 2, 2021 - Use cautionDrug
The Harvard Drug Group recalls NIFEdipine EXTENDED-RELEASE TABLETS, USP 30 mg Rx only packaged as a) 100 count unit dose carton, NDC 0904-7080-61; b)
The Harvard Drug Group recalls specific lots of Nifedipine 30mg extended-release tablets due to failed dissolution specifications. Check your lot numbers and expiration dates.
The Harvard Drug GroupJul 2, 2021
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