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
35,004 found- Lower riskMedical device
Siemens Healthcare Diagnostics Inc recalls RP500e Handheld Barcode Scanner, Zebra Model: DS4308 - HC0062BZZWW, Siemens Material Number (SMN) 11416778
Siemens Healthcare Diagnostics recalls RP500e scanners with Zebra DS4308 model HC0062BZZWW for potential barcode data errors. Affected units may not confirm check-digit integrity when scanning Code 39 barcodes.
Siemens HealthcareMay 27, 2020 - Lower riskMedical device
Prodimed Plastimed Division recalls Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH PE 85 cm x 4.0 mm 58124 40US
Prodimed recalls Combicath catheters for mini bronchoalve: Lavage (BAL) due to lack of sterility assurance. All units within expiry date are affected.
ProdimedMay 27, 2020 - Lower riskDrug
Apotex Inc. recalls Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, 100 count bottles, Rx Only Manufactured by: Apotex, Inc.
Apotex recalls 500mg extended-release metformin tablets due to NDMA impurity exceeding safe levels. This may pose health risks with long-term use. Consumers should contact Apotex for details.
ApotexMay 27, 2020 - UnratedDrug
Pfizer Inc. recalls Duavee (conjugated estrogens/bazedoxifene) tablets 0.45/20 mg, packaged in 2 blister cards containing 15 tablets each
Pfizer recalls Duavee (conjugated estrogens/bazedoxifene) tablets 0.45/20 mg with failed dissolution specifications. Rx-only medication distributed by Wyeth in Ireland. No remedy specified in recall notice.
PfizerMay 27, 2020 - Use cautionConsumer product
Sanvall Enterprises Recalls Rapid Alivio Pain Relieving Roll-On Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
Sanvall recalls Rapid Alivio Pain Relieving Roll-On for non-child-resistant packaging, risking poisoning if young children swallow. Consumers should store out of reach and get a refund.
SanvallMay 27, 2020 - Use cautionConsumer product
Primark Recalls Kitten Heel Court Shoes Due to High Levels of Chromium; Risk of Skin Irritation
Primark recalls Wide Fit Kitten Heel Court Shoes with high chromium levels that may cause skin irritation. Return shoes for full refund at any store.
PrimarkMay 27, 2020 - Use cautionVehicle
KEYSTONE COUGAR (2020) recall — Equipment
Keystone is recalling certain 2020-2021 Cougar travel trailers with Furrion cooktops due to potential flame inversion during furnace operation, risking fire and injury. Owners should contact customer service for free repairs.
KeystoneMay 26, 2020 - Use cautionMedical device
Smiths Medical ASD Inc. recalls Pediatric Adjustable Flange Tracheostomy Tube Cuffless
Smiths Medical recalls pediatric tracheostomy tubes with incorrect neck flange size. This may cause breathing issues if used improperly. Affected units include model 60HA30, lot 37941: 3.5mm ID plate instead of 3.0mm.
Smiths MedicalMay 26, 2020 - Lower riskMedical device
RAYSEARCH LABORATORIES AB recalls RayStation standalone software treatment planning system (RayStation 8A, 8B, 9A, and 9B, including all service packs)
RaySearch Laboratories recalls RayStation software versions 8A-9B due to potential treatment data import errors in radiation therapy systems. Affected users should check their software version and contact support for updates.
RaySearch LaboratoriesMay 26, 2020 - Lower riskMedical device
U&I CORP. recalls ANAX 5.5 Poly-Reduction Screw 6.0X50MM, REF: SFNA6050R, part of ANAX 5.5 SPINAL SYSTEM
U&I CORP. recalls ANAX 5.5 Poly-Reduction Screws with laser etching error that may cause improper fit. Affected units include Lot #19C12063.
U&I CORP.May 26, 2020 - Use cautionMedical device
Radiometer Medical ApS recalls Blood gases (PCO2, PO2) and blood pH test system; ABL800 FLEX; Model Number 393-800; UDI (01)05700693938004. Model
Radiometer recalls ABL800 FLEX blood gas test systems with software versions 6.19 and below due to potential patient mix-up risks. Affected units have specific model numbers and UDI codes.
RadiometerMay 26, 2020 - Lower riskDrug
Jubilant Cadista Pharmaceuticals, Inc. recalls Lamotrigine Tablets, USP, 150 mg, 20,000-count bulk container, Manufactured by: Jubilant Cadista Pharmaceuticals Inc.,
Jubilant Cadista recalls 150mg Lamotrigine tablets with silica granules from desiccant packs. Foreign substance may cause injury. Check lot numbers 19P0437 & 19P0438.
Jubilant CadistaMay 26, 2020 - UnratedDrug
UNICHEM PHARMACEUTICALS USA INC recalls Clonidine Hydrochloride Tablets, USP 0.1 mg 100-count bottles, Rx only, Manufactured by: Unichem Laboratories LTD.
Unichem Pharmaceuticals USA recalls 0.1 mg clonidine tablets due to potential benzophenone migration from containers. These prescription-only tablets were manufactured in India and distributed in the US. Consumers should contact the company for details.
Unichem PharmaceuticalsMay 26, 2020 - UnratedDrug
Aurobindo Pharma USA Inc. recalls Olanzapine Tablets, USP 7.5 mg, 30-count bottle, Rx only, Manufactured for: Prasco Laboratories Mason, OH 45040 USA,
Aurobindo Pharma recalls 7.5mg Olanzapine tablets due to failed impurities and degradation. Rx-only bottles with specific lot number and expiration date are affected. Consumers should contact the manufacturer for details.
Aurobindo PharmaMay 26, 2020 - Lower riskMedical device
Shanghai United Imaging Healthcare Co., Ltd. recalls Computed Tomography X-ray System, Model: uCT 550, GTIN: 06971576831036 Intended use The uCT Computed Tomography X-ray
Shanghai United Imaging Healthcare recalls uCT 550 CT scanners with serial numbers 353020-353023 (software R001.11.0.729741-Re-1100) due to potential false channel marking causing extra radiation exposure and rescan needs.
Shanghai United Imaging HealthcareMay 23, 2020 - Stop using nowMeat & poultry
Conagra Brands, Inc. Recalls Frozen Not-Ready-To-Eat Chicken and Turkey Bowl Products due to Possible Foreign Matter Contamination
Conagra recalls frozen chicken and turkey bowl products that may contain small rocks. Consumers are urged not to eat these items and should discard or return them.
ConagraMay 22, 2020 - Use cautionVehicle
TRIPLE E UNITY (2020) recall — Structure
Triple E is recalling 2020 Unity travel trailers with a locked utility compartment that may prevent access to propane shutoff valve, increasing fire risk during leaks.
Triple EMay 22, 2020 - Use cautionVehicle
FOREST RIVER SURVEYOR (2020) recall — Equipment
Forest River recalls 2020-2021 Surveyor Travel Trailers with unsafe safety chains that may break, causing detachment and injury. Owners must have chains replaced free by June 8, 2020.
Forest RiverMay 22, 2020 - Lower riskMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as interface to the FUJIFILM Synapse PACS Software
Fujifilm recalls specific versions of Synapse PACS software (5.5.x and 5.7.x) due to potential incorrect 3D Tomo slider bar markers, which could lead to misdiagnosis. Affected units have unique serial numbers listed.
FujifilmMay 22, 2020 - Lower riskMedical device
Abbott recalls TactiCath Quartz Contact Force Ablation Catheter, Model Numbers: PN-004 065 (GTIN 07640157990033) and PN-004 075 (GTIN
Abbott recalls TactiCath Quartz Contact Force Ablation Catheters with model PN-004 065 and PN-004 075 due to reported loss of contact force information during use, which may affect heart procedures.
AbbottMay 22, 2020 - Lower riskMedical device
Tosoh Bioscience Inc recalls AIA-900 Analyzer, Part no. 022930, UDI 04560189283992
Tosoh Bioscience recalls AIA-900 Analyzers with serial numbers 10030810 and higher due to a substrate monitoring system that may not detect empty bottles, leading to incorrect test results.
Tosoh BioscienceMay 22, 2020 - Stop using nowMedical device
Siemens Medical Solutions USA, Inc. recalls ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F
Siemens recalls ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F due to left atrial perforations and Atrioventricular Node block. Affected units have specific serial numbers.
SiemensMay 22, 2020 - Use cautionDrug
The Harvard Drug Group recalls Doxycycline Hyclate Tablets, USP, 100 mg, packaged in a) 3x10 unit dose cartons (NDC 0904-0430-04) and b) 5 x 10 unit
The Harvard Drug Group is recalling specific lots of Doxycycline Hyclate Tablets, USP, 100 mg due to failed dissolution specifications at the end of shelf life.
The Harvard Drug GroupMay 22, 2020 - Stop using nowDrug
Acella Pharmaceuticals, LLC recalls NP Thyroid 60, Thyroid Tablets, USP, 1 grain (60 mg), 100-count bottles, Rx Only, Manufactured For: Acella
Acella Pharmaceuticals recalls 100-count NP Thyroid 60 tablets (60 mg) due to superpotent drug risk. Rx-only medication with specific lot numbers and expiration date.
AcellaMay 22, 2020 - Lower riskDrug
Teva Pharmaceuticals USA recalls Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets ( Mixed
Teva Pharmaceuticals USA recalls 5mg amphetamine tablets with possible mixed strengths. Consumers should check product details and contact the company for guidance.
Teva PharmaceuticalsMay 22, 2020 - Use cautionVehicle
CHEVROLET TRAILBLAZER (2021) recall — Tires
General Motors recalls 2021 Chevrolet Trailblazer vehicles with optional 17-inch sport terrain tires due to missing tire pressure labels, which could increase crash risk if inflated incorrectly.
ChevroletMay 21, 2020 - Lower riskMedical device
Elekta Limited recalls Elekta Unity, Philips Marlin Software versions: R5.3.30, R5.3.31, R6.0.5331, R5.7.0, R5.7.1, R6.1.571
Elekta recalls specific software versions for Unity system due to potential contour data mismatch in motion monitoring workflows, which could affect treatment accuracy.
ElektaMay 21, 2020 - Lower riskMedical device
Vitalconnect Inc. recalls VistaSolution, physiological signal transmitter. A software graphical user interface for use by healthcare
Vitalconnect recalls VistaSolution physiological signal transmitter due to software defect that could cause brief hypoxia. Affected units have catalog number 620:2.1 and UDI 00850490007139.
VitalconnectMay 21, 2020 - Stop using nowFood
Captain Rusty's Seafood Products LLC recalls Captain Rusty's Smoked Mahi Dip, Made with real Mahi meat, Keep Refrigerated, 6 lb.
Captain Rusty's recalls 6 lb. Smoked Mahi Dip due to undeclared egg and soy allergens. Check lot codes and expiration dates immediately.
Captain Rusty'sMay 21, 2020 - Use cautionConsumer product
Viva Doria Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
Viva Doria recalls wintergreen essential oil due to non-child-resistant packaging, risking poisoning for young children. Consumers should store out of reach and contact for refunds.
Viva DoriaMay 21, 2020
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