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
34,960 found- Use cautionMedical device
Medtronic Navigation, Inc. recalls Medtronic Nexframe Stereotactic System and StealthStation Cranial software version 3.0 or newer with StealthStation DBS
Medtronic recalls stereotactic surgery systems and software versions 3.0+ that may cause inaccurate brain implant lead placement during deep brain stimulation procedures. Affected units include specific models with O-arm imaging systems.
MedtronicAug 9, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Proteus XR/a (SlOK : K993090)
GE Healthcare recalls Proteus XR/a stationary radiographic systems due to intermittent failure to provide audible exposure indication after imaging. Affected units may not alert users to completed exposures, potentially leading to safety risks during medical procedures.
GE HealthcareAug 9, 2019 - Lower riskMedical device
Medline Industries Inc recalls Medline SYRINGE, PISTON,IRR TRAY,W/.9, REF DYNC2303. Sterile Piston Irrigation Syringe Tray with Saline
Medline recalls sterile piston irrigation syringe trays with incomplete or open packaging seals. Affected units may have compromised sterility.
MedlineAug 9, 2019 - Lower riskMedical device
Implant Direct Sybron Manufacturing, LLC recalls Implant Direct, REF: 833708, Legacy 2 Implant, Surface: HA, 3.7mmD x 8mmL, 3.5mmD Platform, RxOnly, Sterile R, Made in
Implant Direct recalls Legacy 2 dental implants due to incorrect Healing Collar packaging. Affected units may have safety risks from improper implant delivery.
Implant DirectAug 9, 2019 - Lower riskMedical device
Nobel Biocare Usa Llc recalls Esthetic Abutment CC RP 1.5 mm pre-manufactured prosthetic components directly connected to the endosseous implant,
Nobel Biocare recalls Esthetic Abutment CC RP 1.5mm dental implants due to potential screw loosening. Affected units may require retightening with correct screws to prevent complications.
Nobel BiocareAug 9, 2019 - Lower riskMedical device
Randox Laboratories Ltd. recalls Liquid Protein Calibrators (SP CAL (LIQ)) Catalogue Number: IT2691 GTIN: 05055273204032 Product Usage: Liquid Protein
Randox recalls liquid protein calibrators (SP CAL (LIQ)) due to inaccurate Rheumatoid Factor measurements. Affected units may cause incorrect test results for certain blood tests.
RandoxAug 9, 2019 - UnratedDrug
American Health Packaging recalls Carbamazepine, Extended-Release Tablets, USP, 400 mg, 30 Tablets (3 blister cards x 10 unit doses), Rx Only,
American Health Packaging recalls 400mg Carbamazepine extended-release tablets due to failed dissolution specifications. Rx-only medication distributed with NDC 68084-562-21. No remedy specified in recall notice.
American Health PackagingAug 9, 2019 - UnratedDrug
Ridge Properties, LLC recalls PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Liquid Gel, 4%, packaged in a) 1 Oz (NDC 69804-019-14), b) 2
Ridge Properties LLC recalls PRE-TAT 4% lidocaine tattoo prep gel due to microbial contamination. Products may have unsafe lidocaine levels. Consumers should contact the manufacturer for details.
Ridge PropertiesAug 9, 2019 - Lower riskFood
Whole Foods Market recalls 365 Organic Maple & Brown Sugar Pecan Instant Oatmeal 2.3 oz (65 g) microwaveable cups that are sold individually
Whole Foods Market recalls 365 Organic Maple & Brown Sugar Pecan Instant Oatmeal microwaveable cups sold individually due to undeclared pecans. Check for lot code *144S03 or best by date 06/21/20.
Whole Foods MarketAug 9, 2019 - Use cautionFood
Tri-Union Frozen Products, Inc. recalls Cracked Pepper Chicken of the Sea Wild-Caught Pink Salmon Skinless and Boneless, 2.5 oz (70 g) pouch: Shelf Stable UPC
Tri-Union Frozen Products recalls Chicken of the Sea Cracked Pepper Pink Salmon pouches due to bloating from microbial activity. Check expiry dates.
Chicken of the SeaAug 9, 2019 - Lower riskFood
Vitony Bakery, Inc. recalls Vitony Bakery, Brazo Gitano Guayaba Queso (Guava- Cheese Cake Roll); Peso Neto 12 ONZ. (340 G)
Vitony Bakery recalls guava cheese cake rolls due to failure to declare soy, FD&C dyes, and refrigeration requirements. Consumers should check labels for missing soy and color information.
Vitony BakeryAug 9, 2019 - Stop using nowFood
Dole Fresh Vegetables Inc recalls Dole Baby Spinach: 6 oz. (170 g) plastic bag, UPC 0-71430-00964-2, SKU 320; 10 oz. (283 g) clamshell, UPC
Dole Fresh Vegetables Inc recalls Baby Spinach products with Salmonella contamination. Affected items include 6oz plastic bags and 10oz clamshells with specific UPCs and Enjoy by dates. Consumers should stop using these products immediately.
DoleAug 9, 2019 - Use cautionVehicle
IC BUS CESB (2020) recall — Structure
Navistar recalls certain 2019-2020 school buses with roof hatch handles that may break, preventing emergency exit during crises. Owners must have the handle replaced free by dealers.
NavistarAug 8, 2019 - Lower riskMedical device
Foundation Medicine, Inc. recalls FoundationOne CDx test report
Foundation Medicine recalls specific FoundationOne CDx test reports that may show false positive MSI-H results, which could lead to incorrect cancer treatment decisions.
Foundation MedicineAug 8, 2019 - Lower riskMedical device
BioFire Diagnostics, LLC recalls FilmArray Gastronintestinal (GI) Panel, REF: RFIT-ASY-0104, 6-pack kit, UDI (01)00815381020116, CE IVD, Rx Only
BioFire Diagnostics recalls GI Panel kits with false negative results that could lead to incorrect treatment and serious health issues. Affected kits have specific UDI and expiration dates.
BioFire DiagnosticsAug 8, 2019 - Use cautionMedical device
Radiometer Medical ApS recalls AQURE basic sytem, FLEXLINK, REF 933-599, Version: 2.3.3 (17), CE IVD, Rx Only, UDI: (01)05700699335999 Intended use:
Radiometer recalls AQURE basic system (version 2.3.3) due to potential patient data mix-up with third-party devices, risking serious health consequences. Affected units have specific UDI codes.
RadiometerAug 8, 2019 - Lower riskDrug
Alkermes Inc recalls Vivitrol (naltrexone for extended-release injectable suspension) 380 mg/vial. Each Carton Contains: 1) One vial of 380
Alkermes recalls Vivitrol 380mg injectable kits due to 1-inch needles mistakenly included in the 1.5-inch sleeve. This could cause improper injection. Consumers should check their kit's needle size and contact Alkermes for guidance.
AlkermesAug 8, 2019 - Lower riskFood
FIRST START HOLDINGS INC recalls Nosh Organic Fruit & Protein Soft Oat Bar; Apple, Sweet Potato & Cinnamon. 6 - 0.74 oz. (21 g) bars per box. Net Wt.
First Start Holdings recalls Nosh Organic Fruit & Protein Soft Oat Bars (Apple, Sweet Potato & Cinnamon) due to potential mold contamination. Consumers should check product dates and contact for details.
First Start HoldingsAug 8, 2019 - Lower riskFood
Keto Farms LLC recalls Keto Farms Keto Snack Mix - Tomato Pepperjack Fruit & Cheese Mix with Sprouted Pecans & Walnuts; Net Wt. 95 g (3.34 oz.
Keto Farms recalls 95g snack mix due to unlisted coconut allergen. Consumers should check labels for missing allergen declaration.
Keto FarmsAug 8, 2019 - Lower riskMedical device
Integra LifeSciences Corp. recalls Integra Jarit GEMINI CLAMP 9 1/4 inch - used in vascular and cardiothoracic procedures used for clamping and occluding
Integra recalls 9 1/4 inch GEMINI CLAMP for possible corrosion after multiple sterilizations, requiring replacement to prevent breakage during medical procedures.
IntegraAug 7, 2019 - Lower riskMedical device
Aesculap Implant Systems LLC recalls CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM REF: PL730SU - Product Usage: Instrument intended for use in general surgery and
Aesculap recalls specific surgical instruments due to potential insufficient sterilization in certain batches. Affected instruments may pose infection risks during procedures.
Aescul: Aesculap Implant Systems LLCAug 7, 2019 - Lower riskMedical device
Intersurgical Inc recalls Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3503031. Airway connector.
Intersurgical recalls specific Superset airway connectors due to potential port cracks that could leak. Affected units include lot numbers 2180531, 2181808, 2182241, 2182533.
IntersurgicalAug 7, 2019 - Lower riskDrug
Glenmark Pharmaceuticals Inc., USA recalls Clotrimazole and Betamethasone Dipropionate Cream USP, 1%/0.05%, 15 gram tubes, Rx only, Manufactured by: Glenmark
Glenmark recalls 15g Clotrimazole and Betamethasone Dipropionate Cream USP 1%/0.05% tubes due to liquidy texture complaints from temperature abuse.
GlenmarkAug 7, 2019 - UnratedFood
First Rate Plantation recalls Sweet Basil Farm Hawaii
First Rate Plantation recalls Sweet Basil Farm Hawaii (lot #20190722A8) due to FDA-identified Cyclospora cayentanesis contamination. Consumers should check product labels for the lot number.
First Rate PlantationAug 7, 2019 - Stop using nowConsumer product
Seattle Manufacturing Corporation Recalls Ice Axes Due to Serious Injury and Fall Hazards
Seattle Manufacturing Corporation recalls Kobah Ice Axes (60-75cm) due to spike detachment risk during use, potentially causing serious injury or falls. Affected units have orange aluminum handles with black polyamide resin heads.
KobahAug 7, 2019 - Use cautionMeat & poultry
Top Taste Food Warehouse Recalls Meat and Poultry Products Produced Without Benefit of Inspection
Top Taste Food Warehouse recalls pork and chicken dumplings produced without USDA inspection. Consumers are urged not to consume these products and should throw them away or return to purchase location.
Top Taste Food WarehouseAug 6, 2019 - Lower riskMedical device
Preventice Services, LLC recalls BodyGuardian Heart Remote Monitoring Kit, consisting of two BG Heart monitors, either Models BC-1001-A or BC1001-D, and
Preventice recalls BodyGuardian Heart Remote Monitoring Kits with BC-1001-A or BC1001-D monitors that may give inaccurate heart data, risking incorrect health assessments.
PreventiceAug 6, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331
Zimmer Biomet recalls ASI 2.0 Calcar Trimmer Shafts (model 110032331) due to risk of improper mating with Calcar Planar Shaft instruments. Affected units include specific lots.
Zimmer BiometAug 6, 2019 - Use cautionMedical device
Clinical Innovations, LLC recalls Kiwi Complete Vacuum Delivery System, Model No. VAC-6000MTE - Product Usage: The Kiwi is a disposable vacuum-assisted
Clinical Innovations recalls Kiwi Complete Vacuum Delivery System Model VAC-6000MTE due to potential vacuum loss or failure during fetal delivery, which could affect safe use.
Clinical InnovationsAug 6, 2019 - Lower riskMedical device
Arrow International Inc recalls 8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard for use with 7.5 - 8 Fr.Catheters Product Code: CDC-29803-1A -
Arrow recalls Blue PSI Kit Cath-Gard for possible incorrect banner card in kit. This may affect catheter use safety. Contact Arrow for details.
ArrowAug 6, 2019
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,517 recalls tracked · 71,995 explained in plain English · 10,969 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.