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 riskDrug
West-Ward Columbus Inc recalls Doxycycline Hyclate Tablets USP, 100 mg, packaged in a) 50-count bottle (NDC 0143-2112-50), b) 500-count bottle (NDC
West-Ward recalls 100mg Doxycycline Hyclate Tablets due to failed dissolution test at 24 months shelf life. These Rx-only tablets may not release medication properly.
West-WardMay 13, 2020 - Lower riskFood
Willamette Valley Pie Company, LLC. recalls Willamette Valley Pie Company Raspberry Rhubarb Pie, packaged in clamshells container, six containers per case. Each
Willamette Valley Pie Company recalls Raspberry Rhubarb Pie due to mislabeling as Raspberry Rhubarb Pie when it contains artificial almond extract, which was not declared on the label.
Willamette Valley Pie CompanyMay 13, 2020 - Stop using nowConsumer product
Hodedah Recalls HI4DR 4-Drawer Chests Due to Tip-Over and Entrapment Hazards; Remedies May Be Delayed Due to COVID-19 Restrictions; Keep Product Away from Children
Hodedah recalls HI4DR 4-drawer chests due to tip-over and entrapment risks for children. Unanchored chests may cause serious injury or death. Consumers should stop using and secure the chest away from children.
HodedahMay 13, 2020 - Use cautionMeat & poultry
Ideal Foods Recalls Meat and Poultry Flatbread Pizza Products Produced Without Benefit of Inspection
USDA FSIS recalls 3,302 pounds of Ideal Foods flatbread pizza products made without federal inspection. Consumers urged not to eat these items and dispose of them safely.
Ideal FoodsMay 12, 2020 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Raw Beef Ravioli Products Due to Possible E. Coli O157:H7 Contamination
FSIS alerts consumers that approximately 70 pounds of raw beef ravioli products from P&S Ravioli Company may be contaminated with E. coli O157:H7. These products should be thrown away or returned to the place of purchase as they are no longer available for sale.
P&S Ravioli CompanyMay 12, 2020 - Lower riskMedical device
Abbott Gmbh & Co. KG recalls Alinity C, Processing Module. Chemistry analyzer for in-vitro diagnostics.
Abbott recalls Alinity C processing modules for potential incorrect patient results in alkaline phosphatase, amylase, creatine kinase, and gamma glutamyl transferase tests.
AbbottMay 12, 2020 - Use cautionMedical device
XTANT Medical recalls Irix-C Forceps Inserter; Product Code/UDI: T066-0059/ M697T06600591
XTANT Medical recalls Irix-C Forceps Inserter devices with product code T066-0059/ M697T06600591 due to risk of strike plate fracturing from unsatisfactory welds.
XTANT MedicalMay 12, 2020 - Use cautionMedical device
Med Tec Inc recalls Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage: Device is intended for patient
Med Tec recalls Type S Extension devices for patient use due to potential disengagement during repositioning, risking patient falls if not supported by staff.
Med TecMay 12, 2020 - Use cautionMedical device
Medtronic Vascular Galway DBA Medtronic Ireland recalls Medtronic Confida Expandable Sheath, REF CES122230. To provide a guide for catheters or devices introduced into the
Medtronic recalls Confida Expandable Sheath (REF CES122230) due to increased risk of bleeding, hematoma, and dissection. All units with UDI 00763000233815 are affected.
MedtronicMay 12, 2020 - Use cautionMedical device
Covidien Llc recalls Multifire VersaTrack Auto Suture Hernia Stapler, 4.0mm, Part No. 174021 - Product Usage: has application in endoscopic
Covidien recalls Multifire VersaTrack Auto Suture Hernia Stapler (4.0mm, Part No. 174021) due to a manufacturing error that may cause staples to fail advancing when handle is compressed. Affected lots: P9J0241Y, P9J0242Y, P9J0243Y, P9K1140Y, P9K1663Y, P9K1141Y.
CovidienMay 12, 2020 - Lower riskMedical device
DiaSorin Molecular LLC recalls MOL3655 Simplexa VZV Swab Direct - Product Usage: is intended for use on the LIAISON MDX instrument for the qualitative
DiaSorin recalls MOL3655 Simplexa VZV Swab Direct for potential false negative results from a software malfunction in the Multi Assay Suite. Affected lots were sold between September 2019 and February 2021.
DiaSorinMay 12, 2020 - Stop using nowFood
Ramar International Corporation recalls Peekaboo Ice Cream + hidden Veggies; Organic Mint Chocolate Chip with Hidden Spinach, 14 oz. carton: UPC: 868540000115
Ramar International Corporation recalls Peekaboo Ice Cream products with hidden veggies and spinach due to Listeria monocytogenes contamination found in retail stores.
Peekaboo OrganicsMay 12, 2020 - Lower riskFood
Johnson Sea Products, Inc. recalls Home Style Crab Cakes in a plastic wrapped foam tray, 12 oz. (Four, 3 oz. crab cakes per package). 12 packages per case.
Johnson Sea Products recalls 12 packages of Home Style Crab Cakes due to undeclared wheat and soybean oil on product label. Consumers should check batch numbers for affected items.
Johnson Sea ProductsMay 12, 2020 - Use cautionVehicle
NISSAN ALTIMA (2020) recall — Tires
Nissan is recalling certain 2020 Altima S models with Continental ProContact TX tires (size 215/60 R16 H) due to potential over-curing causing sidewall breaks or tread separation, increasing crash risk. Free tire replacements offered.
NissanMay 11, 2020 - Use cautionVehicle
LAND ROVER DISCOVERY SPORT (2020) recall — Electrical System
Land Rover is recalling 2020 Discovery Sport vehicles with electrical short-circuit risk. Owners must exit vehicle when parked and park away from structures until software update completes.
Land RoverMay 11, 2020 - Use cautionVehicle
BUICK ENCLAVE (2020) recall — Tires
GM recalls 2020 Buick Enclaves with Continental tires that may overcure, causing sudden air loss or tread/belt loss. Owners must have tires inspected and replaced free of charge by dealers.
BuickMay 11, 2020 - Use cautionMedical device
Radiometer Medical ApS recalls ABL80-FLEX CO-OX 393-841 Box Label, REF 393-841, IVD, CE, UDI: 05700693938417 - Product Usage: It is intended for use
Radiometer recalls ABL80-FLEX CO-OX 393-841 lab equipment due to barcode misreads causing patient mix-ups or delayed treatment. All units affected.
RadiometerMay 11, 2020 - Use cautionMedical device
Biomet, Inc. recalls Comprehensive VRS Inserter, shoulder prosthesis, Item No. 110019068. UDI: (01)00880304829503 (10)814100,
Biomet recalls shoulder prosthesis inserters with specific serial numbers due to potential screw drill seizure causing extended surgery. Affected units include items with UDI codes (01)00880304829503 and lots 814100, 570640, 728890, 977300.
BiometMay 11, 2020 - Lower riskMedical device
Ortho-Clinical Diagnostics recalls VITROS Chemistry Product Performance Verifier I, Product Code 8231474, UDI # 10758750004577 - Product Usage: For in
Ortho-Clinical Diagnostics recalls VITROS Chemistry Product Performance Verifier I due to imprecise control fluid measurements affecting lab test accuracy. Affected units may show inconsistent results with expected standards.
Ortho-Clinical DiagnosticsMay 11, 2020 - Lower riskDrug
Torrent Pharma Inc. recalls Carbamazepine Tablets, USP 200 mg, packaged in a 500-count bottle, Rx only, Manufactured by: Torrent Pharmaceuticals
Torrent Pharma recalls 200mg Carbamazepine tablets with failed dissolution specs. Rx-only 500-count bottles may not release medication properly. Consumers should contact pharmacy for guidance.
TorrentMay 11, 2020 - UnratedDrug
BIOTA Biosciences LLC recalls Sterile Cannabidiol (CBD) + Curcumin 50mg/mL, 10 mL vial
BIOTA Biosciences recalls sterile CBD and curcumin vials due to unapproved ingredients and lack of FDA approval. Consumers should check lot numbers and contact the company for details.
BIOTA BiosciencesMay 11, 2020 - Use cautionVehicle
YAMAHA YZF-R3 (2016) recall — Visibility
Yamaha recalls 2015-2020 YZF-R3 scooters with less reflective rear reflectors that may reduce visibility, increasing crash risk. Owners will receive free rear reflector replacements.
YamahaMay 10, 2020 - Use cautionVehicle
KIA FORTE (2019) recall — Power Train
Kia is recalling 2019 Forte vehicles with potentially unheat-treated left front axle driveshafts that could break, increasing crash risk. Owners must have driveshaft inspected and replaced if needed.
KiaMay 8, 2020 - Use cautionVehicle
THOR MOTOR COACH FOUR WINDS (2020) recall — Seat Belts
Thor Motor Coach recalls 2020-2021 Four Winds motorhomes with faulty seat belt anchorages that could fail during crashes, increasing injury risk. Owners must have pedestal bolts inspected by dealers.
Thor Motor CoachMay 8, 2020 - Lower riskMedical device
Shanghai United Imaging Healthcare Co., Ltd. recalls uCT 530 Computed Tomography X-Ray System
Shanghai United Imaging Healthcare recalls uCT 530 CT scanners with software version R001.11.0.729741-Re-1100 due to potential false channel marking and radiation exposure risks from rescan needs.
Shanghai United Imaging HealthcareMay 8, 2020 - Use cautionMedical device
Arrow International Inc recalls Arrow FlexTip Plus Epidural Kit with NRFit Connector, catheter system, Product Codes (US) OT19TAGSK OT19TAGSKA
Arrow recalls FlexTip Plus Epidural Kits with NRFit Connector due to reported rotatable collar detachment causing leaks. Affected units include specific product codes and distribution lots.
ArrowMay 8, 2020 - Lower riskMedical device
Shanghai United Imaging Healthcare Co., Ltd. recalls uCT 760 System, Computed Tomography X-ray System
Shanghai United Imaging Healthcare recalls uCT 760 CT scanners with specific serial numbers and software versions due to potential image artifacts and radiation dose increases from rescanning.
Shanghai United Imaging HealthcareMay 8, 2020 - Lower riskMedical device
Merge Healthcare, Inc. recalls Merge Healthcare Merge Application Server Software Release and Merge Healthcare Merge Cardio Workstation Software
Merge Healthcare recalls specific software versions due to potential inaccurate Z-Score calculations that could lead to false negative results in medical testing. Affected users should check their software versions and contact the company for guidance.
Merge HealthcareMay 8, 2020 - Lower riskMedical device
Ge Healthcare recalls The OEC 9900 C-Arm is designed to provide fluoroscopic and spot-film images of the patient during diagnostic, surgical
GE Healthcare recalls OEC 9900 C-Arm fluoroscopy systems in the US that may not display required dose values per regulations. Affected units were configured to show AKR/CAK instead of DAP when leaving the factory.
GE HealthcareMay 8, 2020 - Stop using nowDrug
ICU Medical Inc recalls LACTATED RINGER'S Injection, USP 1000 mL flexible container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC
ICU Medical recalls Lactated Ringer's 1000mL injection due to iron oxide particles found in some units. Affected lots expire July 2021. No remedy specified in recall notice.
ICU MedicalMay 8, 2020
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83,592 recalls tracked · 72,039 explained in plain English · 10,976 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.