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- Use cautionDrug
The Medicine Shoppe Pharmacy recalls Bi-Est (1:1)/Progesterone/Testosterone 2.5/150/1.5 mg/mL Versabase CR 90 mL bottle, Rx, The Medicine Shoppe Pharmacy,
The Medicine Shoppe Pharmacy recalls one bottle of Bi-Est (1:1)/Progesterone/Testosterone due to lack of processing control. Check your lot number.
The Medicine Shoppe PharmacyApr 6, 2020 - Lower riskFood
GOLDEN NUTRITION INC recalls Biotin 1000mcg, Dietary Supplement, 30 Tablets, Manufactured by: Golden Nutrition
Golden Nutrition recalls Biotin 1000mcg tablets (Lot #1345) because the biotin content is only 0.8% of the label claim.
Golden NutritionApr 6, 2020 - Stop using nowConsumer product
Joybird Recalls Dressers Due to Tip-Over and Entrapment Hazards
Joybird recalls Blythe dressers that may tip over or entrap children, causing serious injury or death. Unanchored dressers don't meet safety standards. Consumers should stop using and contact Joybird for repair or refund.
JoybirdApr 6, 2020 - Use cautionVehicle
HYUNDAI GENESIS COUPE (2016) recall — Air Bags
Hyundai recalls 2016 Genesis Coupe vehicles with potentially detachable driver air bags that could cause injury in a crash. Owners must have bolts inspected and retightened by dealers.
HyundaiApr 5, 2020 - Use cautionVehicle
PETERBILT 520 (2020) recall — Service Brakes, Air
PACCAR recalls 2016-2020 Peterbilt 520 trucks with potential brake delay risk. Vehicles may fail FMVSS 121 air brake standards. Owners must have brakes checked by dealers for free.
PeterbiltApr 3, 2020 - Use cautionVehicle
PETERBILT 365 (2020) recall — Electrical System
PACCAR recalls 2015-2020 Peterbilt 365, 389, 567, and 579 trucks with a left-hand under hood jumper terminal that may cause electrical short circuits and fire risk. Owners must have terminals inspected and replaced free.
PeterbiltApr 3, 2020 - Lower riskMedical device
Immersivetouch Inc recalls ImmersiveView software version 2.1 Product Usage: ImmersiveView is intended as pre-operative software for simulating
Immersivetouch recalls software version 2.1 for pre-operative surgical simulation due to a repetitive software glitch. Users should contact the company for details.
ImmersivetouchApr 3, 2020 - Use cautionMedical device
C.A. Greiner & Sohne Gesellschaftmbh recalls VACUETTE Blood Transfer Unit. Lot no. A19024NX. Expiration date: 2022-02-07 - Product Usage: The Blood Transfer Unit is
C.A. Greiner recalls VACUETTE Blood Transfer Units with lot A19024NX (expired Feb 2022) due to needle dislodgement causing potential needle stick injuries or blood leakage during blood transfer.
C.A. GreinerApr 3, 2020 - Lower riskMedical device
Pega Medical Inc. recalls Orthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Product Usage: The SLIM
Pega Medical recalls SLIM handle instruments with mismatched lot numbers to prevent surgical errors. Affected items have lot code B204-1 on handle but B204-01 on packaging.
Pega MedicalApr 3, 2020 - Lower riskMedical device
Skeletal Kinetics, Llc recalls Cranio/Sculpt C, 10cc, Bone Void Filler, UDI: 00813845021129 - Product Usage: CRANIO/SCULPT C is a calcium phosphate
Skeletal Kinetics recalls Cranio/Sculpt C 10cc bone void filler due to potential mix-up with unsterilized OsteoVation EX. Affected units have UDI 00813845021129. No action needed if product was used properly.
Skeletal KineticsApr 3, 2020 - Lower riskMedical device
Philips North America, LLC recalls Philips Azurion 7 M20 -XperGuide Software hosted in Interventional Workspot 1.5 when used with the Azurion R2.0 system
Philips recalls Azurion 7 M20 software with Azurion R2.0 system for incorrect X-ray overlays if L-arm isn't repositioned during live guidance. Affected units have specific serial numbers.
PhilipsApr 3, 2020 - Use cautionMedical device
Heartware, Inc. recalls Heartware HVAD Pump Implant Kit, Product (REF) Number 1103
Heartware recalls HVAD Pump Implant Kit (REF 1103) due to risk of outflow graft tears and strain relief screw breakage during pre-implant assembly. Affected units have specific serial numbers and GTINs listed. Consumers should check their device details and contact Heartware for guidance.
HeartwareApr 3, 2020 - UnratedDrug
Golden State Medical Supply Inc. recalls Losartan Potassium Tablets, USP, 25 mg, Rx only, a) 30 ct. (NDC 60429-316-30) b) 90ct. (NDC 60429-316-90) c) 1,000 ct.
Golden State Medical Supply recalls 25mg Losartan Potassium Tablets (NDC 60429-316-30, 90ct, 1000ct) due to impurity detected in active ingredient. Consumers should contact the company for details.
Golden State Medical SupplyApr 3, 2020 - Use cautionVehicle
HYUNDAI ELANTRA TOURING (2011) recall — Service Brakes, Hydraulic
Hyundai recalls 2011 Elantra Touring vehicles with potential engine compartment fire from ABS module electrical short. Owners must have relay installed by dealer to prevent fire risk.
HyundaiApr 2, 2020 - Lower riskMedical device
Abbott Laboratories recalls Accelerator APS Aliquoter Module, List number: 07L40 - Product Usage: The ACCELERATOR APS Workcell is a modular system
Abbott recalls Accelerator APS Aliquoter Module (List 07L40) due to potential sample dilution from AQM clot detection errors, which could cause incorrect lab results. Affected units include all field serial numbers.
AbbottApr 2, 2020 - Lower riskMedical device
Insulet Corporation recalls Omnipod DASH Insulin Management System (mg/dL configuration), Catalog Number PT000010 M/D: INT1D001MG - Product Usage:
Insulet recalls Omnipod DASH insulin systems with mg/dL configuration due to potential bolus calculation errors after 2 months of use. Affected units may require replacement.
InsuletApr 2, 2020 - Lower riskMedical device
GE Healthcare, LLC recalls Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001 GTIN: 00840682110808.
GE Healthcare recalls Giraffe Shuttle Upgrade Kits with part numbers 2109672-001 and 2109673-001 due to sulfur odor from battery outgassing during charging. Affected units have specific serial numbers and GTIN.
GE HealthcareApr 2, 2020 - Lower riskMedical device
Osteomed, LLC recalls OSTEOVATIONEX 3CC INJECT FORMULA. REF/UDI: 390-0003/00813845020016 - Product Usage: The product provides a bone void
Osteomed recalls OSTEOVATIONEX 3CC bone void filler kits that may not maintain setting characteristics for the labeled shelf-life. Affected kits have specific lot numbers.
OsteomedApr 2, 2020 - Stop using nowConsumer product
VP Harrier and Giant Pinner Bicycle Pedals Recalled Due to Fall and Injury Hazards; Made by VP Components
VP Components recalls Harrier and Giant Pinner DH bicycle pedals due to spindle separation. Stop using immediately for free replacement.
VP ComponentsApr 2, 2020 - Stop using nowConsumer product
Stelpro Design Recalls Sonoma Wall Fan Heaters Due to Fire Hazard
Stelpro recalls ASSO and ASSOS Sonoma wall fan heaters with version codes 47-19 or older due to fire hazard. Consumers must stop using and get free replacements.
StelproApr 2, 2020 - Stop using nowConsumer product
Southern Motion Recalls "Wireless Power" Reclining Furniture Due to Fire Hazard
Southern Motion recalls Wireless Power reclining furniture with lithium-ion batteries that can overheat and cause fire. Consumers must stop using immediately and get free in-home repair.
Southern MotionApr 2, 2020 - Stop using nowConsumer product
Manhattan Toy Recalls Musical Lili Llama Due to Choking Hazard
Manhattan Toy recalls Musical Lili Llama wooden toy due to screws falling off and posing choking hazard for young children. Consumers should stop using and contact for free repair kit.
Manhattan ToyApr 2, 2020 - Use cautionMedical device
Howmedica Osteonics Corp. recalls Cortoss Bone Augmentation Material, Catalog Nos. 2101-0005 and 2101-0010
Howmedica recalls Cortoss Bone Augmentation Material (Catalogs 2101-0005 and 2101-0010) due to potential nerve damage and embolism from improper refrigeration.
HowmedicaApr 1, 2020 - UnratedMedical device
Abbott Laboratories recalls ARCHITECT C Peptide Calibrator - Product Usage: used as an aid in the diagnosis and treatment of patients with abnormal
Abbott recalls ARCHITECT C Peptide Calibrators due to Mexico license renewal documentation error. All units until new license is obtained are affected. No immediate action needed.
AbbottApr 1, 2020 - Lower riskMedical device
Ortho-Clinical Diagnostics recalls VITROS Chemistry Products CKMB Slides, Creatine Kinase MB, Product Code 8001133-90 slides, UDI Number 10758750004201 -
Ortho-Clinical Diagnostics recalls VITROS CKMB Slides (Product Code 8001133-90) due to false plasma test results in Spanish/Swedish language versions of instructions. Affected units expire after July 20, 2018.
Ortho-Clinical DiagnosticsApr 1, 2020 - Stop using nowMedical device
Aesculap Implant Systems LLC recalls PRESTIGE RETRACTION GRASPER, W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8361-10
Aesculap recalls Prestige Retraction Graspers with potential handle separation. Affected models include 8361-10 (UDI-DI: 04046955083381) sold in specific lots. Stop using immediately to avoid injury.
AesculapApr 1, 2020 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore,
Lupin Pharmaceuticals recalls 30mg Lisinopril tablets due to foreign 5mg tablets found in some bottles. This may cause incorrect dosing. Check your bottle's lot number and contact the company for details.
Lupin PharmaceuticalsApr 1, 2020 - Stop using nowFood
Homestead Creamery, Inc. recalls Homestead Creamery Unsalted Butter. 0.45 lb. net weight. 1 unit per package, cellophane wrap
Homestead Creamery recalls unsalted butter with potential Listeria monocytogenes contamination. Consumers should avoid using this product due to food safety risks.
Homestead CreameryApr 1, 2020 - Use cautionFood
Rong Shing Trading NY Inc recalls XinXing Dried Plum, Net Wt. 5.3 oz.(150g)
Rong Shing Trading recalls XinXing Dried Plum because it contains dried peaches, posing an allergy risk. Check your UPC and best-before date.
XinXingApr 1, 2020 - Use cautionVehicle
SUBARU CROSSTREK (2019) recall — Seat Belts
Subaru is recalling 2019 Crosstrek vehicles with rear seat belts that may not lock properly during multi-impact crashes, increasing injury risk. Owners can get free replacements.
SubaruMar 31, 2020
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