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
34,894 found- Stop using nowConsumer product
Saber Grills Recalls Grills and LP Regulators Due to Fire and Burn Hazards
Saber recalls LP grills and regulators with model numbers RA329 and date codes 1120-1344 due to fire and burn risks from gas leaks. Consumers must stop using and contact Saber for free repairs.
SaberSep 26, 2017 - Use cautionVehicle
FORD F-650 SD (2015) recall — Steering
Ford is recalling 2015 F-650 trucks with potentially loose tie rods that could cause loss of steering control at low speeds. Owners should contact Ford for free inspection.
FordSep 25, 2017 - Use cautionVehicle
FORD F-550 SD (2017) recall — Seats
Ford is recalling 2017 F-550 SD trucks with manually adjusted front passenger seats due to potential seat belt buckle weld failure, which could increase injury risk in crashes. Owners must have the front passenger seat track replaced free of charge.
FordSep 25, 2017 - Use cautionVehicle
FORD F-150 (2018) recall — Structure
Ford is recalling 2018 F-150 Raptor Super Cabs without moonroofs due to missing roof brace rivets that could reduce structural integrity during rollover crashes. Owners must contact Ford for free roof brace repairs.
FordSep 25, 2017 - Lower riskMedical device
Leica Microsystems, Inc. recalls PROVEO 8 Ophthalmic Microscope System optical instrument for improving the visibility of objects through magnification
Leica recalls PROVEO 8 Ophthalmic Microscope Systems with specific serial numbers due to potential focus movement interruptions and display failures during medical use. Affected units may require professional evaluation.
LeicaSep 25, 2017 - Lower riskMedical device
Smiths Medical ASD Inc. recalls CADD(TM) Medication Cassette Reservoir with clamp and female Luer., Nonvented stopper included., 100 mL, For use with
Smiths Medical recalls certain CADD medication cassette reservoirs with a potential incorrect pressure plate that could cause malfunction. Affected units include all lot numbers for 100mL reservoirs used with CADD pumps (excluding specific models).
Smiths MedicalSep 25, 2017 - Lower riskMedical device
Resource Optimization & Innovation Llc recalls Regard Custom Surgical Pack Packs contain surgical instruments and accessories intended for use during a surgical
Resource Optimization & Innovation recalls Regard Custom Surgical Packs with incorrect ChloraPrep labels that could lead to wrong surgical solution use. Affected units have a "ChloraPrep One-Step" label instead of "ChloraPrep With Tint".
Resource Optimization & InnovationSep 25, 2017 - Lower riskMedical device
PerkinElmer Life and Analytical Sciences, Wallac, OY recalls AutoDELFIA Neonatal immunoreactive trypsin(ogen) (IRT) kit, intended for the quantitative determination of human
PerkinElmer recalls AutoDELFIA Neonatal IRT kits with missing Quality Control Certificate that may delay test results. Affected kits have specific UDI and expiration dates.
PerkinEl:merSep 25, 2017 - Use cautionMedical device
W L Gore & Associates, Inc. recalls GORE TAG, THORACIC ENDOPROSTHESIS, CONFORMABLE. The GORE TAG Thoracic Endoprosthesis is intended for endovascular
W L Gore recalls GORE TAG Thoracic Endoprosthesis with serial numbers starting TGE212110. Incomplete deployment during surgery may cause complications. Affected patients should contact the manufacturer for details.
W L GoreSep 25, 2017 - Lower riskDrug
Sandoz Inc recalls Ampicillin for Injection, USP, 500 mg per vial, single vial (NDC 0781-3407-78) packaged in 10-count shrink wrap packs
Sandoz recalls 10-count packs of Ampicillin injections (500mg/vial) due to missing labels on some vials. This could lead to incorrect dosing if used without proper labeling.
SandozSep 25, 2017 - Use cautionDrug
Amneal Pharmaceuticals, Inc. recalls Esterified Estrogens & Methyltestosterone Tablets, USP 1.25 mg/2.5 mg, 100-count bottles, Rx Only, Manufactured by:
Amneal recalls 19,176 bottles of Esterified Estrogens & Methyltestosterone Tablets due to subpotent drug levels. Check your lot numbers and expiration date.
Amneal PharmaceuticalsSep 25, 2017 - Lower riskDrug
Precision Dose Inc. recalls Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per
Precision Dose recalls 10-count carbamazepine oral suspension cups due to low drug potency. This may result in ineffective treatment. Check your product details and contact the manufacturer for guidance.
Precision DoseSep 25, 2017 - Use cautionDrug
RXQ Compounding LLC recalls methylPREDNIsolone ACETATE, 40 MG/ML INJECTION SUSPENSION, 10 ML Vial, RXQ Compounding, Athens, OH --- NDC:
RXQ Compounding recalls methylprednisolone acetate injection vials due to potential contamination from improper autoclave sterilization. Affected lots produced in Athens, OH with specific NDC and expiration dates.
RXQ CompoundingSep 25, 2017 - Lower riskFood
Chun Yuen Trading Co., Inc. recalls Instant Reishi Coffee, 4 in 1; Ca Phe Ling Chi; 20 sachets, Net Wt. 360g (12.7 oz.) UPC 8 93663 00225 8 Ingredients:
Chun Yuen Trading Co. recalls 20-sachet Instant Reishi Coffee products due to milk not being declared on labels. Consumers should check for the UPC 8 93663 00225 8.
Chun Yuen TradingSep 25, 2017 - Stop using nowConsumer product
Pro-Tec Recalls Multisport Helmets Due to Risk of Head Injury
Pro-Tec recalls City Lite and Street Lite adult multisport helmets due to buckle failure causing head injury risk. Consumers must stop using and return for refund.
Pro-TecSep 25, 2017 - Stop using nowConsumer product
Delta Recalls Strollers Due to Fall Hazard
Delta recalls J is for Jeep cross-country strollers with a risk of falling due to a potentially broken leg bracket. Consumers must stop using and contact Delta for free repairs.
J is for JeepSep 25, 2017 - Use cautionVehicle
BMW F800 GT (2015) recall — Equipment
BMW recalls 2014-2016 F800 GT and 2015-2016 F800 R motorcycles due to rear reflectors not being visible in traffic, violating FMVSS 108. Owners must have license plate holder modified for free.
BMWSep 22, 2017 - Use cautionVehicle
MERCEDES-BENZ SPRINTER 2500 (2016) recall — Power Train
Daimler Vans USA is recalling 2016 Mercedes-Benz Sprinter 2500 vehicles with a missing driveshaft catch strap that could cause fuel leaks and fire risk. Owners must contact DVUSA for free repairs.
Mercedes-BenzSep 22, 2017 - Use cautionVehicle
KENWORTH T800 (2016) recall — Steering
PACCAR recalls 2016 Kenworth T800 trucks with potentially loose steering tie rods that could cause loss of steering and crash risk. Owners must have dealer inspect torque or replace parts.
KenworthSep 22, 2017 - Use cautionVehicle
MERCEDES-BENZ METRIS (2017) recall — Steering
Daimler Vans USA recalls 2015-2017 Mercedes-Benz Metris vans with improperly welded power steering pins that may deactivate steering assist, increasing crash risk. Owners will receive free rack replacement.
Mercedes-BenzSep 22, 2017 - Use cautionVehicle
JAYCO GREYHAWK (2017) recall — Equipment
Jayco is recalling 2016-2017 Greyhawk motorhomes with damaged liquid propane lines that could cause fire. Owners should contact Jayco for free repairs or replacements.
JaycoSep 22, 2017 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls BARD MAX-CORE Disposable Core Biopsy Instrument, Product Codes - MC1410, 14 g x 10 cm; MC1616, 16 g x 16 cm; MC1816, 18
Bard recalls MAX-CORE Disposable Core Biopsy Instruments with specific model codes due to increased complaints of failure to prime, fire, obtain samples, or self-activation.
BardSep 22, 2017 - Lower riskMedical device
Guangzhou Improve Medical Instruments Co., Ltd. recalls Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO
Guangzhou Improve Medical Instruments recalls Prevent G Safety Winged Blood Collection Sets due to leak complaints. Affected units have serial number 102030178 and lot number 16080:160809.
Prevent GSep 22, 2017 - Lower riskMedical device
Guangzhou Improve Medical Instruments Co., Ltd. recalls Prevent G Safety Winged Blood Collection Set Glide - Rx Only -Sterile/EO - Product Usage: The IMPROSAFE Blood
Guangzhou Improve Medical Instruments recalls Prevent G Safety Winged Blood Collection Set Glide due to risk of hub needle detaching during blood draw. Affected units have serial # 102030178 and lot # 160815. No remedy specified in recall notice.
Guangzhou Improve Medical InstrumentsSep 22, 2017 - Stop using nowMedical device
Circulatory Technology Inc recalls **Recall Expanded to add these models: Bigger Better-Bladder cardiopulmonary bypass blood reservoir; Models: BBB38
Circulatory Technology recalls Bigger Better-Bladder cardiopulmonary bypass blood reservoirs (BBB38 and BBB38NS) due to potential collapse during use, which may cause reduced blood flow in ECMO circuits.
Circulatory TechnologySep 22, 2017 - Lower riskMedical device
Ortho-Clinical Diagnostics recalls VITROS Chemistry Products DAT Performance Verifier IV in vitro diagnostic
Ortho-Clinical Diagnostics recalls VITROS DAT Performance Verifier IV in vitro diagnostics due to incorrect storage labeling causing lower than expected BENZ results. Affected units have catalog #6802330 and lot #L5619.
Ortho-Clinical DiagnosticsSep 22, 2017 - UnratedMedical device
Angiodynamics, Inc. recalls Soft-Vu Omni Flush Angiographic Catheter (UPN H787107322015); SV OF 5F x 65 cm .035 NB PG; Catalog Number: 10732201
Angiodynamics recalls Soft-Vu Omni Flush Angiographic Catheters due to incomplete post-sterilization release activities. Affected units may have safety risks during medical procedures.
AngiodynamicsSep 22, 2017 - Lower riskMedical device
Boston Scientific Corporation recalls Auriga XL 4007 Laser System, Universal Part Number: M0068FS4007G0. Intended to be used in surgical procedures.
Boston Scientific recalls Auriga XL 4007 Laser System with serial numbers 20509715, 20465096, etc. due to incorrect trigger wire assembly causing error codes or console failure during surgery.
Boston ScientificSep 22, 2017 - Lower riskDrug
Boehringer Ingelheim Pharmaceuticals, Inc. recalls Mobic (meloxicam) tablets, 15 mg, package in 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim (BI)
Boehringer Ingelheim recalls Mobic 15mg tablets with incorrect or missing package inserts. Affected lots may not have proper instructions for safe use.
Boehringer IngelheimSep 22, 2017 - Use cautionFood
The Kroger Co recalls Chicken Salad Sandwich 6.8 oz plastic container Contains: Wheat, Egg, Soy USPC 6 63209-02050 9
Kroger recalls chicken salad sandwiches from 09/20/2017 to 09/28/2017 due to Listeria monocytogenes contamination. Consumers should check sell-by dates and avoid use if symptoms appear.
The Kroger CoSep 22, 2017
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