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- Lower riskFood
Driscoll's Inc. recalls Driscoll's Conventional Strawberries (Fresh) packed in 8x16oz clamshell and 4X32oz clamshell; 8 clamshells per case, 4
Driscoll's recalls conventional strawberries with pesticide residue exceeding U.S. safety limits. Consumers should check lot numbers from harvest dates in January 2022.
Driscoll'sJan 21, 2022 - Lower riskFood
ARILLIS CORP recalls Tortillas Arillis, Arillis Corp, Contains: 10 (ten) tortillas
Arillis Corp recalls 10-tortilla packages due to undeclared wheat allergen. Consumers may face allergic reactions if they have wheat sensitivity.
ArillisJan 21, 2022 - Use cautionVehicle
HEARTLAND CYCLONE (2021) recall — Tires
Heartland is recalling 2021 Cyclone vehicles with specific Sailun tires due to potential belt separation causing loss of vehicle control. Owners must have tires inspected and replaced if needed.
HeartlandJan 20, 2022 - Lower riskMedical device
Outset Medical, Inc. recalls Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000
Outset Medical recalls two models of hemodialysis consoles (PN-0003000 and PN-0006000) due to a component that may cause heat-related damage. Affected units have specific serial numbers and UDI codes listed in the recall notice.
Outset MedicalJan 20, 2022 - Lower riskMedical device
Microgenics Corporation recalls QMS Tacrolimus Immunoassay REF 10015573 CALIBRATOR SET QMS TACROLIMUS CAL A 10015566-3 QMS TACROLIMUS CAL B 10015567-3
Microgenics recalls QMS Tacrolimus calibrators that may over-quantitate tacrolimus patient results, leading to inaccurate medication levels. Affected units include specific model numbers and lot numbers.
MicrogenicsJan 20, 2022 - Use cautionMedical device
Ventana Medical Systems Inc recalls BenchMark ULTRA and DISCOVERY ULTRA Instruments
Ventana Medical Systems recalls BenchMark Ultra and Discovery Ultra instruments with serial numbers <= 322030 due to potential fluid leaks causing electrical shorts and fire risks.
Ventana Medical SystemsJan 20, 2022 - Lower riskMedical device
SIGHT DIAGNOSTICS LTD recalls The Sight OLO device is a computer vision based platform for blood analysis. The platform combines computer-vision
Sight Diagnostics recalls The Sight OLO blood analysis device with software versions 2.59.3 and earlier may display incorrect reference range values after custom configuration. Affected units have specific serial numbers listed in the recall notice.
Sight DiagnosticsJan 20, 2022 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5
Bard recalls pediatric lumbar puncture trays with potential manometer leaks. Affected units have specific lot numbers; stop using immediately to prevent injury.
BardJan 20, 2022 - Lower riskMedical device
Envisiontec US Llc recalls PCA 4000 Curing Units, SKU number ACC-06-1000 The PCA 4000 is used for curing industrial resins as well and this recall
Envisiontec recalls PCA 4000 curing units (SKU ACC-06-1000) that may not fully cure dental resins to specifications. Affected units sold to dental professionals.
EnvisiontecJan 20, 2022 - Lower riskMedical device
Surgical Innovations Ltd recalls Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001. For use in laparoscopic procedures.
Surgical Innovations recalls YelloPort Plus 5x70 Cannula + Luer devices for laparoscopic use due to non-sterile condition despite sterile labeling. This may increase infection risk during surgery.
Surgical InnovationsJan 20, 2022 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls Diagnostic Ultrasound System, ACUSON Juniper, UDI: (01)04056869152059, Model: 11335791, Rx, CE Ultrasound imaging
Siemens Medical Solutions recalls ACUSON Juniper ultrasound systems with serial numbers 550010-554118. The clip store function may fail when disk full, potentially delaying critical treatment during high-risk procedures like stress echo exams.
SiemensJan 19, 2022 - Lower riskMedical device
Volcano Corporation recalls SyncVision Systems, Model: 400-0100.10, PN: 30000485688x, with software version 4.2.x
Volcano recalls SyncVision Systems with software version 4.2.x due to potential incorrect iFR/FFR co-registration results, which could lead to inappropriate patient treatment. Affected units have specific serial numbers and software versions.
VolcanoJan 19, 2022 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Azacitidine, 1,00mg/Vial, One Single-dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530
Dr. Reddy's recalls certain Azacitidine vials due to failed stability specifications. This may affect drug effectiveness and safety. Check NDC 43598-305-62 and specific lot numbers for affected products.
Dr. Reddy'sJan 19, 2022 - Lower riskFood
Amys Kitchen Inc recalls Amy's Vegan Organic Rice Mac & Cheese; frozen; 8 oz. (227 g) individually packaged serving; in trays with plastic
Amy's Kitchen recalls vegan rice mac and cheese due to trace milk detected in frozen servings. Products sold in 8-oz individual packs with plastic overwrap. No remedy specified in official notice.
Amy's KitchenJan 19, 2022 - Lower riskFood
B.C.S. International Corporation recalls Dr. Snack Goji Berry; PACKED FOR B.C.S. INTERNATIONAL CORP; 4.5oz, 6oz, 9oz packs clear plastic packs and 5lb cardboard
B.C.S. International recalls Goji Berry snacks due to undeclared sulfites. Check UPCs 80555492205, 80555493218, 80555494216, or 80555470198 for affected products.
B.C.S. InternationalJan 19, 2022 - Lower riskFood
Fetting's Frozen Foods LLC recalls Abbys Bakery Homestyle White Bread Dough. Product number 93596. Keep Frozen. 4-1 lb. loaves. Net Wt. 4 lbs. (1.81kg)
Abbys Bakery Homestyle White Bread Dough (product #93596) may contain glass. Recalled items were sold in 4-lb loaves with lot codes 21340-31 to 21340-36. Keep frozen until 6/6/2022.
Abbys BakeryJan 19, 2022 - UnratedFood
Frozen Food Development Inc recalls Steamable by Lidl Chopped Spinach NET WT 12 OZ (340 g) UPC 4 056489 34380 6. Frozen product.
Lidl recalls frozen chopped spinach due to possible Listeria monocytogenes contamination. Consumers should check product UPC 4 056489 34380 6 and use by 9/10/23.
LidlJan 19, 2022 - Stop using nowConsumer product
Mushie & Co Recalls FRIGG Silicone Pacifiers Due to Choking Hazard
Mushie & Co recalls FRIGG silicone pacifiers due to a choking hazard. The nipple can detach from the shield. Stop use and contact Mushie for a refund.
MushieJan 19, 2022 - Stop using nowConsumer product
Children's Sleepwear Garments Recalled by Childrensalon Due to Violation of Federal Flammability Standards and Burn Hazard
Childrensalon recalls five brands of children's sleepwear due to flammability standards violation. Stop using immediately and contact the retailer for a refund.
ChildrensalonJan 19, 2022 - Use cautionVehicle
PETERBILT 579 (2022) recall — Structure
PACCAR recalls 2022 Peterbilt 579 trucks with unsecured cab steps that can unexpectedly move, increasing injury risk during entry/exit. Owners must contact dealers for free repairs.
PeterbiltJan 18, 2022 - Use cautionMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls LINQ II Insertable Cardiac Monitor
Medtronic recalls 8 LINQ II Insertable Cardiac Monitors that may lose functionality due to moisture ingress. Affected devices have specific serial numbers and GTINs.
MedtronicJan 18, 2022 - Lower riskMedical device
Merete Medical GmbH recalls Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only
Merete Medical recalls PediatrOS RigidTack size 20mm due to incorrect marketing label (25mm) applied. This affects products sold with the wrong size marking.
Merete MedicalJan 18, 2022 - Lower riskMedical device
Cytocell Ltd. recalls Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions in chromosome location from patients with AML
Cytocell recalls Del(5q) FISH Probe Kit for incorrect color labeling that could lead to wrong results in AML/MDS chromosome testing. Affected kits have red and green probes swapped.
Cytoc:ellJan 18, 2022 - Lower riskDrug
Teva Pharmaceuticals USA recalls Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10 mg/10 mg, 100-count bottle, Rx Only,
Teva Pharmaceuticals USA recalls 100-count doxylamine succinate/pyridoxine hydrochloride tablets due to failed dissolution specification. This may affect medication effectiveness. Check NDC 0591-2132-01 and lots 100025842, 100028023.
Teva Pharmaceuticals USAJan 18, 2022 - Lower riskFood
Walla Walla Cheese Company LLC recalls Walla Walla Cheese Company Mad Curds. Keep Refrigerated. Product is packaged in vacuum sealed zip lock bags - net wt. 5
Walla Walla Cheese Company recalls Mad Curds due to under-pasteurized milk. Product sold in vacuum-sealed bags with no expiration date. Keep refrigerated until use.
Walla Walla Cheese CompanyJan 18, 2022 - Use cautionVehicle
KEYSTONE ALPINE (2022) recall — Structure
Keystone is recalling 2022 Alpine RVs with ladders not securely attached to the rear wall. This could cause detachment during use, leading to injury. Owners must have ladders reattached by dealers.
KeystoneJan 17, 2022 - Lower riskMedical device
Lacrimedics Inc recalls Collagen Plugs, CP3, 0.3mm, CP4, 0.4mm, CP5, 0.5 mm, Sterile, EO, Rx Only, CE Dry eye treatment
Lacrimedics recalls specific collagen plug models due to potential pouch seal issues that could compromise sterility. Affected products include CP3, CP4, and CP5 dry eye treatments with certain lot numbers.
LacrimedicsJan 17, 2022 - Use cautionVehicle
FOREST RIVER CHEROKEE (2022) recall — Tires
Forest River recalls 2022 Cherokee Toy Haulers with potentially incorrect tire installation that could increase crash risk. Owners receive free replacement tires and placards.
Forest RiverJan 14, 2022 - Use cautionVehicle
FORD F-650 (2021) recall — Fuel System, Diesel
Ford recalls 2021 F-650 trucks with potential fuel leaks that could cause fire if near ignition sources. Owners must get free fuel filter replacement.
FordJan 14, 2022 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement
Maquet recalls HEMASHIELD Gold vascular grafts with mismatched labeling that could disrupt blood vessel repairs, risking pseudo-aneurysms. Affected units have specific size and lot numbers.
MaquetJan 14, 2022
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83,807 recalls tracked · 72,041 explained in plain English · 10,992 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.