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
35,069 found- Use cautionVehicle
COACHMEN CLIPPER (2021) recall — Equipment
Forest River recalls 2021 Coachmen Viking and Clipper travel trailers due to potential fire risk from inverted flames in the cooktop. Owners must have a panel and seal installed by dealers.
Forest RiverDec 3, 2021 - Lower riskMedical device
Konica Minolta Healthcare Americas, Inc. recalls ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing and presentation of medical images on
Konica Minolta recalls ImagePilot software versions 1.92 and 1.93 for medical imaging systems due to potential incorrect length/area calculations if power sequence is incorrect. Affected units include specific product and software versions.
Konica MinoltaDec 3, 2021 - Lower riskMedical device
Wright Medical Technology, Inc. recalls Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE
Wright Medical recalls Charlotte MTP Hex Screw Model 411: Incorrect product in packaging. Affected units sold with specific lot numbers. Contact for replacement.
Wright MedicalDec 3, 2021 - Lower riskMedical device
Wright Medical Technology Inc recalls Stryker DARCO Screw, Locking, Ti6A14V, REF DC2825016, 2.7mm x 16mm.
Wright Medical recalls Stryker DARCO Screw (REF DC2825016) due to incorrect product in packaging. Affected units may contain wrong item; contact for details.
Wright MedicalDec 3, 2021 - Lower riskDrug
Gilead Sciences, Inc. recalls Veklury (remdesivir) for injection, 100 mg/vial, Single-Dose Vial, Rx only, Manufactured for: Gilead Sciences, Inc.,
Gilead Sciences recalls Veklury (remdesivir) 100mg vials due to glass particles found in some batches. This could cause injury if injected. Affected vials have specific lot numbers and expiration dates.
Gilead SciencesDec 3, 2021 - UnratedDrug
Valgene Incorporated dba Cape Drugs recalls B-Complex, injection, 1 mL vials, Rx only, Cape Drugs 1384 Cape St. Claire Road Annapolis, MD 21409
Cape Drugs recalls B-Complex injections due to lack of processing controls. Affected lots were sold at Cape Drugs locations in Annapolis, MD. Consumers should check product labels for lot number 190036.
Cape DrugsDec 3, 2021 - Lower riskDrug
Akorn, Inc. recalls Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles, Rx only, Hi-Tech Pharmacal Co., Inc.,
Akorn recalls 30mL Morphine Sulfate Oral Solution bottles (Rx only) due to missing labels. This could lead to incorrect dosing if used without proper labeling.
AkornDec 3, 2021 - Use cautionDrug
Dental Alliance Holdings LLC recalls CTx7 Kit, contains one tube CariFree CTx4 Gel 5000, 1.1% Neutral Sodium Fluoride Mint, 2 oz (57 g) Rx only NDC:
Dental Alliance Holdings LLC recalls specific lots of the CTx7 Kit because the CTx4 gel contains less sodium fluoride than labeled.
CariFreeDec 3, 2021 - Lower riskFood
Slayer Forever, LLC dba BUBS Naturals recalls BUBS Naturals Fountain of Youth Formula; Collagen Protein; Support for Hair, Skin & Nails; Biotin, Antioxidant, Vitamin
BUBS Naturals recalls fountain of youth formula due to undeclared milk in MCT oil powder. Consumers should check lot numbers and contact the company for details.
BUBS NaturalsDec 3, 2021 - Use cautionVehicle
NEWMAR VENTANA (2021) recall — Service Brakes, Hydraulic
Newmar recalls 2021 Ventana motorhomes with potentially loose brake caliper bolts that could reduce braking effectiveness and increase crash risk. Owners must contact Newmar for free repair.
NewmarDec 2, 2021 - Use cautionVehicle
FREIGHTLINER CASCADIA (2021) recall — Engine
Daimler Trucks North America recalls 2021 Freightliner Cascadia trucks with Cummins X15 engines due to risk of detached flywheel causing loss of power and potential crash. Owners must have capscrews inspected and repaired free of charge by dealers.
Daimler Trucks North AmericaDec 2, 2021 - Lower riskMedical device
CELLTRION USA INC recalls Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
Celltrion USA recalls RUO COVID-19 test kits (CT-P60 D-2 02) shipped to customers by mistake. These kits are for research only and not approved for clinical use. No action needed as they are not intended for home use.
CelltrionDec 2, 2021 - Use cautionMedical device
Natus Neurology DBA Excel Tech., Ltd. (XLTEK) recalls IPELA FHD PTZ TILE KITS with Axis cameras used in combination with Natus Neuroworks/Sleepworks software
Natus Neurology recalls IPELA FHD PTZ Tile Kits with Axis cameras used in sleep monitoring software. Ceiling tiles may fall causing injury. Check serial numbers for affected units.
Natus NeurologyDec 2, 2021 - Lower riskMedical device
LivaNova USA, Inc. recalls Vagus Nerve Stimulation (VNS) Therapy Leads, PerenniaDURA, Model: 303. Model 303-20 PereniaDURA Lead (2.0 mm electrode
LivaNova recalls VNS therapy leads model 303 due to potential silicone tubing wall thickness issues that could cause lead breach and discomfort or loss of therapy.
LivaNovaDec 2, 2021 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Zenition 50, Model #718096
Philips recalls Zenition 50 surgical systems with wireless foot switch model #718096 due to firmware issues that may cause procedure delays if the hand or wired switches aren't used.
PhilipsDec 2, 2021 - Lower riskDrug
Torrent Pharma Inc. recalls Carbamazepine Tablets, USP 200 mg 100 Tablets Rx only NDC 13668-268-01 Manufactured by: Torrent Pharmaceuticals Ltd.
Torrent Pharma recalls 200mg Carbamazepine tablets (NDC 13668-268-01) due to failed dissolution specifications. This may affect medication effectiveness. Contact for return instructions.
Torrent PharmaDec 2, 2021 - Lower riskMedical device
MEDLINE INDUSTRIES, LP - Northfield recalls Michels Transport Medium, 20ML Prefilled Cont
Medline recalls 20ML prefilled Michels Transport Medium with expiration dates from 08/28/2021 to 09/03/2023 due to potential improper storage in temperature-controlled settings instead of refrigeration.
MedlineDec 1, 2021 - Lower riskMedical device
MEDLINE INDUSTRIES, LP - Northfield recalls Premier Rotaclone, Rx only
Medline Industries recalls Premier Rotaclone (Rx only) due to potential improper storage in temperature-controlled settings instead of refrigeration. This may affect product safety.
Medline IndustriesDec 1, 2021 - UnratedMedical device
CELLTRION USA INC recalls Celltrion DiaTrust COVID-19 Ag Rapid Test, REF CT-P60 D-2 01. Contains 25 disposable test tubes with extraction buffer,
Celltrion USA recalls DiaTrust COVID-19 Ag Rapid Test (REF CT-P60 D-2 01) as it was illegally distributed in the U.S. without U.S. approval. The European version has different packaging and labeling not authorized for U.S. distribution.
CelltrionDec 1, 2021 - Lower riskMedical device
MEDLINE INDUSTRIES, LP - Northfield recalls HARDY DIAGNOSTICS CatScreen, 25dsk/vial
Hardy Diagnostics CatScreen 25-disk/vial (Model HADZ110) recalled due to improper storage in temperature-controlled settings instead of refrigeration. No remedy specified.
Hardy DiagnosticsDec 1, 2021 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls Hemashield Gold Knitted Bifurcated, 18 mm x 9 mm; reference number M002020851890
Maquet recalls Hemashield Gold Knitted Bifurcated Vascular Grafts (18mm x 9mm) due to probable mislabeling with Platinum models. Affected units may contain incorrect product specifications.
MaquetDec 1, 2021 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH ¿2-Microglobulin (B2M) -M) Assay for in vitro diagnostic use in the quantitative determination of
Siemens Healthcare recalls Atellica B2M assay lot 211446 due to potential inaccurate results. This may lead to misdiagnosis of kidney disease. Affected units have specific Siemens material numbers and lot numbers.
Siemens HealthcareDec 1, 2021 - UnratedDrug
Torrent Pharma Inc. recalls Telmisartan and Hydrochlorothiazide Tablets, USP, 40 mg/12.5 mg, 30 count bottles, Rx only, Manufactured by: Torrent
Torrent Pharma recalls 40mg/12.5mg Telmisartan and Hydrochlorothiazide tablets due to superpotent hydrochlorothiazide risk. Rx-only bottles with specific NDC and batch numbers affected.
TorrentDec 1, 2021 - Lower riskFood
MORTON SALT INC recalls Morton Iodized Salt, Net Wt. 26 oz (1 LB 10 OZ) 737 g, Morton Salt, Inc. Chicago, IL 60606
Morton Iodized Salt (26 oz) recalled as it does not contain iodine. This affects salt used for dietary needs in areas where iodine is required.
MortonDec 1, 2021 - Use cautionFood
Livia Global recalls Livia One Organic Daily Topical Spray Probiotics; 4 oz. (120 ml) UPC: 0 30915 10710 5 Recommended use: Topical: Spray
Livia Global recalls 4 oz. probiotic spray due to Pseudomonas aeruginosa contamination. Stop using if you have the affected lot.
Livia GlobalDec 1, 2021 - Stop using nowConsumer product
Halo Recalls Promotional Children's Projector Flashlights Due to Button Battery Ingestion and Choking Hazards
Halo recalls five children's projector flashlight models due to button battery ingestion and choking hazards. Consumers should stop using and return items for a $5 gift card.
HaloDec 1, 2021 - Stop using nowConsumer product
E-filliate Recalls DEWALT Wireless Earphones Due to Burn and Fire Hazards
DEWALT Jobsite Pro Wireless Earphones with specific manufacture codes recalled due to overheating risks of burns and fires. Consumers must stop using and return for free replacement.
DEWALTDec 1, 2021 - Lower riskMedical device
MEDLINE INDUSTRIES, LP - Northfield recalls Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls, Ref. No. 2460-605
Medline recalls Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls shipped without refrigeration. Affected units may degrade test results. Contact Medline for details.
MedlineNov 30, 2021 - Lower riskMedical device
Straumann USA LLC recalls Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 Article Number: 138.107
Straumann recalls Neodent Easypack Helix GM Acqua 3.5x13mm implants that were mislabeled as 3.5x8mm. This mislabeling could lead to incorrect implant placement. Affected units have specific article numbers and lot codes.
StraumannNov 30, 2021 - Lower riskMedical device
ROi CPS LLC recalls Regard, T AND A - Rogers, sterilized convenience kits
ROi CPS recalls sterilized convenience kits with missing rubber latex warning labels. Affected kits may not alert users to latex allergy risks. Contact for replacement.
ROi CPSNov 30, 2021
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