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Latest recalls
34,894 found- Stop using nowConsumer product
John Deere Recalls Compact Utility Tractors Due To Crash and Injury Hazards (Recall Alert)
John Deere recalls 2025R compact utility tractors with brake failure risk. Affected units have serial numbers from 1LV2025R×HJ100101 to 101005. Consumers must stop using and contact a dealer for free repair.
John DeereJan 31, 2018 - Use cautionVehicle
AUDI A3 (2013) recall — Air Bags
Volkswagen recalls 2013 Audi A3s with driver air bag inflator that may explode in crashes, risking serious injury or death. Owners must have inflator replaced free by dealer.
AudiJan 30, 2018 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2015) recall — Equipment
Daimler Trucks North America recalls certain 2002-2017 Thomas Built Buses Saf-T-Liner C2 school buses with Kidde fire extinguishers that may become clogged or detach, increasing fire injury risk. Owners must contact Kidde for a free replacement by March 30, 2018.
Thomas Built BusesJan 30, 2018 - Use cautionVehicle
JAYCO PRECEPT (2017) recall — Service Brakes, Hydraulic
Jayco is recalling 2017 Precept motorhomes with potential brake fluid leaks due to missing valve block ball plugs. Owners should contact Jayco for free brake system inspection.
JaycoJan 30, 2018 - Use cautionVehicle
ENTEGRA INSIGNIA (2017) recall — Service Brakes, Air
Entegra is recalling 2017 Insignia motorhomes with undersized air brake reservoirs that may cause reduced braking and crash risk. Owners must contact Entegra or Spartan for free replacement.
EntegraJan 30, 2018 - Use cautionVehicle
FOREST RIVER GEORGETOWN (2018) recall — Electrical System
Forest River recalls 2018 Georgetown RVs with 18-gauge wiring that may overheat and cause fire. Owners must have wiring checked by dealers by Feb 20, 2018.
Forest RiverJan 30, 2018 - Lower riskMedical device
Howmedica Osteonics Corp. recalls Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee system devices are sterile, single-use
Howmedica recalls Triathlon Revision Knee implants (Catalog #5545-A-3:301 and #5546-A-601) due to risk of receiving incorrect size implants. Affected patients should contact Howmedica for evaluation.
HowmedicaJan 30, 2018 - Use cautionMedical device
Encore Medical, Lp recalls AltiVate Reverse INSTRUMENTATION, HUMERAL SOCKET SHELL TRIAL, STANDARD, REF 804-06-152, Qty: 01, Encore Medical, LP
Encore Medical recalls AltiVate Humeral Socket Shell Trial (REF 803-06-152) due to broken screws and retaining clips that may cause injury during surgery.
Encore MedicalJan 30, 2018 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Dimension Vista¿ Calcium Flex¿ reagent cartridge, Dimension Vista¿ CA, K1023, SMN # 10445160 The CA method is an in
Siemens Healthcare recalls Dimension Vista Calcium Flex reagent cartridges that may produce erroneously low calcium test results. Affected units include specific model numbers and lots. Consumers should contact Siemens for details.
Siemens HealthcareJan 30, 2018 - Lower riskMedical device
Orthofix Srl recalls TL-HEX TruLok Hexapod System, Double Row Footplates, TL-HEX Sterile, All Sizes: 120 MM, 140 MM, 160 MM, 180 MM, 200 MM.
Orthofix recalls specific sizes of TL-HEX TruLok Hexapod System footplates due to incompatibility with newer struts, potentially causing improper bone alignment during healing.
OrthofixJan 30, 2018 - Use cautionDrug
Millennium Pharmaceuticals Inc. recalls VELCADE (bortezomib) for injection, 3.5 mg/vial, Reconstitution Information, SUBCUTANEOUS INJECTION ONLY add 1.4 mL
Millennium Pharmaceuticals recalls VELCADE 3.5mg vials with loose vial crimps that could lead to injury during injection. Affected vials have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
Millennium PharmaceuticalsJan 30, 2018 - Lower riskFood
Sumano's Bakery recalls Sourdough French: Product number 2044; SKU 61659799; GTIN [00046567600932] ; UPC 831 49000044 20 pieces; Ingredients:
Sumano's Bakery recalls 20-piece sourdough French bread due to customer reports of small metal pieces found on the outside before baking. This could pose a choking hazard if ingested.
Sumano's BakeryJan 30, 2018 - Use cautionConsumer product
Walgreens Pain and Itch Relief Cream Recalled by Natureplex Due to Failure to Meet Child Resistant Closure Requirement
Recalled Well at Walgreens pain and itch relief cream (4% lidocaine) lacks child-resistant packaging, risking poisoning for young children. Return to Walgreens for refund.
NatureplexJan 30, 2018 - Use cautionVehicle
HARLEY-DAVIDSON VRSCDX (2011) recall — Service Brakes, Hydraulic
Harley-Davidson recalls 2011 VRSCDX motorcycles with ABS brakes due to brake fluid deposits that may cause valve sticking and reduce braking ability, increasing crash risk. Owners must have brake system flushed with new fluid.
Harley-DavidsonJan 29, 2018 - Lower riskMedical device
Stryker Communications recalls Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000. Product Usage: Chromophare surgical
Stryker is a leading global manufacturer of medical devices and healthcare products. The company has a long history of innovation and quality in the healthcare industry.
StrykerJan 29, 2018 - Lower riskMedical device
Beckman Coulter Inc. recalls AQUIOS CL Flow Cytometer System, Catalog #B30166. The AQUIOS CL Flow Cytometer system is an automated analyzer that use
Beckman Coulter recalls AQUIOS CL Flow Cytometer System (Catalog #B30166) due to potential for incorrect test results from misidentified samples. Affected units may need correction.
Beckman CoulterJan 29, 2018 - Lower riskMedical device
NxStage Medical, Inc. recalls NxStage Dialysate Sack: 1) REF SAK-301 UDI-M535SAK3010, 2) REF SAK-302 UDI-M535SAK3020, 3) REF SAK-303 UDI-M535SAK3030,
NxStage recalls specific dialysate sacks due to potential endotoxin levels exceeding safety standards for hemodialysis use. Affected units include SAK-301 to SAK-407 with specific lot numbers and expiration dates.
NxStageJan 29, 2018 - Use cautionMedical device
Philips Electronics North America Corporation recalls Philips QCPR Meter - used with FR3 Product Usage: The Philips CPR meter is intended for use with the Philips HeartStart
Philips recalls QCPR meters used with HeartStart FR3 defibrillators due to risks of improper pad placement during CPR. Affected models include 861444, 861332, and others. Correct placement is critical for effective CPR.
PhilipsJan 29, 2018 - UnratedMedical device
Encore Medical, Lp recalls Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 50mm, REF 804-07-500 Product Usage: The AltiVate
Encore Medical recalls Altivate Anatomic Shoulder Implants (size 50mm) due to a design flaw where pegs may not align properly with implants during surgery, potentially causing complications. Affected units include specific part numbers.
Encore MedicalJan 29, 2018 - Lower riskDrug
Mckesson Packaging Services recalls Megestrol Acetate Oral Suspension, USP 400 mg/ 10mL (10 mL UD cups in boxes of 20 cups), Rx Only, Dist. By McKesson
Mckesson Packaging Services recalls Megestrol Acetate Oral Suspension (400 mg/10mL) due to subpotent drug levels. This prescription medication may not contain enough active ingredient. Contact for details.
Mckesson Packaging ServicesJan 29, 2018 - UnratedDrug
Teva Pharmaceuticals USA recalls Fentanyl Transdermal System. 25 mcg/h, packaged in 5 pouch system cartons (NDC 0591-3198-72), Rx Only, Manufactured by:
Teva recalls Fentanyl Transdermal System (25 mcg/h) due to potential Fentanyl-n-Oxide impurities exceeding safety limits. Rx-only product with specific lot numbers and expiration dates.
Teva Pharmaceuticals USAJan 29, 2018 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets 10 mg, a) 90 count and b) 500 count bottles, Rx only, Mfd by: Dr. Reddy's Laboratories,
Dr. Reddy's recalls 10mg Atorvastatin Calcium tablets with impurities detected. Affected lots from March 2018 and May 2018. Stop using if you have these specific bottles.
Dr. Reddy'sJan 29, 2018 - Lower riskFood
Despana Brand Foods recalls DON BOCARTE ARTE EN EL PALADAR MIGAS BONITO DEL NORTE PESCA SELECTA DEL CANTABRICO; UPC: 8 43700227144
Despana Brand Foods recalls MIGAS BONITO DEL NORTE product due to possible elevated histamine levels. Consumers should check UPC 843700227144 and lot 33613 for affected items.
DespanaJan 29, 2018 - Lower riskFood
Kingston Pharma LLC recalls Live Better Drug Free Black Elderberry Syrup, 4 FL OZ (118 mL); DIETARY SUPPLEMENT, UPC 050428581186
Kingston Pharma recalls Live Better Drug Free Black Elderberry Syrup due to gas developing in sealed bottles. Consumers should check UPC 050428581186 for affected products.
Kingston PharmaJan 29, 2018 - UnratedFood
IQ PRODUCE, LLC recalls Fresh Fragrant Pear; Label - Double Trees Product of China Shenzhen J.F. Fruit Co., LTD
IQ PRODUCE recalls Fresh Fragrant Pears imported from China with unapproved pesticide isocarbophos. Consumers should avoid these pears due to potential health risks from pesticide exposure.
IQ PRODUCEJan 27, 2018 - Use cautionVehicle
MITSUBISHI LANCER (2010) recall — Visibility
Mitsubishi recalls 2010 Lancer models with sunroofs due to potential sunroof glass detachment while driving, creating road hazards. Owners must have the sunroof glass replaced free by dealers.
MitsubishiJan 26, 2018 - Use cautionVehicle
MITSUBISHI OUTLANDER (2012) recall — Engine And Engine Cooling
Mitsubishi recalls 2012 Outlander vehicles with certain engine belts that may detach, causing engine stall and crash risk. Owners must have belt tensioner replaced free by dealers starting March 27, 2018.
MitsubishiJan 26, 2018 - Use cautionVehicle
MITSUBISHI OUTLANDER SPORT (2016) recall — Parking Brake
Mitsubishi recalls 2016 Outlander Sport vehicles with parking brake that may not engage fully, risking unexpected movement on slopes. Free repairs to prevent crashes.
MitsubishiJan 26, 2018 - Lower riskMedical device
Inova Diagnostics Incorporated recalls QUANTA-Lyser 240 EIA, Part #GS0241. The instrument is a fully automated, high-throughput, bench top system designed for
Inova Diagnostics recalls QUANTA-Lyser 240 EIA (Part #GS0241) due to faulty power supply causing loss of protective grounding. Affected units may have electrical damage risks.
Inova DiagnosticsJan 26, 2018 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls ACUSON SC2000 Ultrasound System Product Usage: The SC2000 ultrasound imaging system is intended for the following
Siemens recalls ACUSON SC2000 ultrasound systems that may underestimate heart blood flow measurements, affecting cardiac diagnoses. Serial numbers listed in the notice.
SiemensJan 26, 2018
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