Archive
590 recalls were announced in July 2020.
Of the 590 recalls this month scored against our rubric, 2% are Critical, 27% are Severe.
Which agencies issued them
Hyundai is recalling 2020 Genesis G70 vehicles because a steering component may be defective, potentially causing the steering to lock or become difficult to operate while driving.
Walmart is recalling specific Hyper Tough 2 Ton Jack Stands that may collapse unexpectedly under load, posing a risk of injury to nearby persons.
Certain 2018-2021 Autocar Xpeditor right-hand drive trucks may have improperly assembled parking brake plumbing, causing the brake to apply unexpectedly and increasing crash risk.
Mercedes-Benz is recalling specific 2017-2019 models because instrument cluster software may cause the seat belt warning system to display a solid light instead of a blinking light with an audible tone.
ZF is recalling air bag crash sensors in 2019 Chrysler Jeep Cherokee and 2018 Volkswagen Atlas vehicles due to manufacturing defects that may delay or prevent air bag deployment.
JBS Food Canada ULC is recalling approximately 38,406 pounds of raw boneless beef head meat products that were imported into the United States without undergoing required FSIS import re-inspection.
General Motors is recalling 2020 Buick, Cadillac, Chevrolet, and GMC vehicles because the roof-rail air bag inflator may separate during deployment, increasing injury risk.
Bio Source Naturals is recalling Wintergreen and Birch Sweet Essential Oils because the packaging is not child-resistant, posing a risk of poisoning to young children.
Miles Industries is recalling about 370 Valor H5 gas fireplaces in the U.S. because delayed ignition can shatter the glass window, posing burn and laceration risks.
Xtreme Outdoors is recalling 2020 Little Guy Mini Max Trailers because understated weight ratings on certification labels may cause trailers to exceed tow vehicle capacity.
Transliquid Technologies is recalling Mystic Shield hand sanitizer bottles due to the presence of undeclared methanol.
Becton Dickinson is recalling SafeStep Huber Needle Sets with GuardIVa Antimicrobial Hemostatic Dressing Port Access Kits due to potential tubing cracks that may cause leakage.
Becton Dickinson is recalling SafeStep Huber Needle Sets because tubing may crack, risking chemical exposure, blood loss, or infection.
Becton Dickinson is recalling PowerLoc MAX infusion sets because tubing may crack, risking leakage of chemicals or biohazard materials.
Becton Dickinson is recalling SafeStep Huber Needle Sets because tubing may crack, risking leakage of chemicals or blood.
Becton Dickinson is recalling PowerLoc MAX infusion sets because tubing cracks may cause leakage of chemicals or biohazard materials.
Winnebago is recalling 2019-2020 Micro Minnie 5 travel trailers because a bedroom emergency exit window was not installed, potentially preventing escape during an emergency.
Lupin Pharmaceuticals is recalling Cefdinir for Oral Suspension due to out-of-specification assay results in retention samples.
Becton Dickinson is recalling SafeStep Huber Needle Sets because tubing may crack or break, risking leakage of chemicals or blood.
Philips is recalling 28 IntelliVue MX700 patient monitors due to defective power supplies that may energize metal parts or prevent operation.
REV Recreation Group is recalling 2019-2020 Fleetwood Pace Arrow motorhomes because loose battery brackets may cause a short circuit and fire.
Boston Scientific is recalling 656 IceForce 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Becton Dickinson is recalling SafeStep Huber Needle Set Port Access Kits because tubing may crack or break, potentially causing leakage of hazardous materials or blood.
Wellspect HealthCare is voluntarily recalling specific LoFric Origo urethral catheters due to a potential defect in the distal tip.
Carefusion 2200 Inc is recalling Thora-Para 5 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Becton Dickinson is recalling PowerLoc MAX infusion sets because tubing may crack, risking chemical exposure, blood loss, or infection.
Sysmex America, Inc. is recalling eight PS-10 Sample Preparation Systems because they may contain insufficient antibody without triggering an error message or alarm.
Carefusion 2200 Inc is recalling Safe-T-Centesis 6 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Wellspect HealthCare is voluntarily recalling specific LoFric Origo urinary catheters because of a potential defect in the distal tip.
Carefusion 2200 Inc is recalling Thora-Para 8 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Becton Dickinson is recalling PowerLoc MAX Power Injectable Infusion Port Access Kits due to potential tubing cracks that may cause leakage of hazardous materials.
Boston Scientific is recalling 79 IceFORCE 2.1 CX Prostate Kits because needle surfaces deteriorated due to unexpected electrolysis during procedures.
Carefusion 2200 Inc is recalling Safe-T 8 Fr Thora-Para Trays because internal valve leaks may introduce up to 30cc of air into patients.
Carefusion is recalling Safe-T PLUS Thora-Para 5 Fr Non-Valved Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling 48 IcePearl 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
BMW is recalling 2020 X3 vehicles because they lack rearview camera software, increasing crash risk when reversing.
Becton Dickinson is recalling SafeStep Huber Needle Sets because tubing may crack or break, potentially causing leakage of chemicals or biohazard materials.
Mevion Medical Systems is recalling eight MEVION S250 Proton Radiation Treatment Systems because a sharp edge on a perforated screen poses an injury risk to service personnel.
Becton Dickinson is recalling PowerLoc MAX Power Injectable Infusion Sets because tubing may crack or break near the Luer or Y site, risking leakage of chemicals or blood.
Carefusion 2200 Inc is recalling Safe-T-Centesis 6 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Carefusion 2200 Inc is recalling Thora-Para 5 Fr Non-Valved Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Carefusion 2200 Inc is recalling Safe-T 5 Fr Thora-Para Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling 71 IceFORCE 2.1 Prostate Cryoablation Kits because needle surfaces deteriorated due to unexpected electrolysis during procedures.
Boston Scientific is recalling IcePearl 2.0 CX 90 Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Carefusion 2200 Inc is recalling Thora-Para 8 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
EHOB, Inc. is recalling 173 Expansion Control Overlays (Item No. 1004EC) because a portion of the lot may have been contaminated with blood.
Chuckanut Bay Foods is recalling 60 Red Velvet Layered Cheesecakes distributed in California because the product contains undeclared walnuts.
Philips is recalling 28 IntelliVue MX800 patient monitors due to defective power supplies that may energize metal parts or prevent operation.
Boston Scientific is recalling 88 Prostate Cryoablation Kits because needle surfaces deteriorated during procedures due to unexpected electrolysis.
Philips is recalling 3,075 IntelliVue G7m Anesthesia Gas Modules due to a firmware issue that may interrupt gas measurement and display.
Becton Dickinson is recalling SafeStep Huber Needle Sets because tubing may crack or break, potentially causing leakage of hazardous chemicals or blood.
Siemens is recalling syngo.via RT Image Suite software versions VB30 and VB40 because modified MR image orientations may result in incorrect geometry and radiation treatment plans.
Carefusion 2200 Inc is recalling Safe-T-Centesis PLUS 6 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling 18,440 IceFORCE 2.1 CX 90 Needle Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Boston Scientific is recalling 39 IceFORCE 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Carefusion 2200 Inc is recalling Safe-T-Centesis PLUS 8 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Wellspect HealthCare is voluntarily recalling LoFric Origo urinary catheters due to a potential defect in the distal tip.
Certain 2020-2021 Thor motorhomes with swivel seats have wiring harnesses that may be routed incorrectly, potentially causing side airbags to deploy inadvertently or fail during crashes. Owners should contact Thor or Mercedes-Benz for free inspection and repair.
Carefusion 2200 Inc is recalling Safe-T PLUS Thora-Para 8 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling 193 IcePearl 2.1 CX Prostate Kits because needle surfaces deteriorated due to unexpected electrolysis during procedures.
Carefusion 2200 Inc is recalling Safe-T-Centesis 8 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Medtronic Xomed is recalling IPC software upgrade v 2.7.3.0 because the M5 Microdebrider may rotate faster than the set value.
Carefusion 2200 Inc is recalling Safe-T PLUS Thora-Para 5 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling 205 IcePearl 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Shanghai United Imaging Healthcare is recalling three uCT 550 CT systems in Texas due to software issues that may cause image artifacts or scanning interruptions.
U&I Corp. is recalling six ANAX 5.5 Poly-Reduction Screws because they were laser etched with the wrong size (6.0x45 instead of 6.0x50).
Medtronic is recalling Accurian RF Ablation Cannulas because the probes catch on a lip inside the hub, causing insertion difficulty.
Smith & Nephew is recalling 12 TRIGEN intramedullary nail sleeves because a manufacturing error led to improper re-sterilization of the polyethylene material.
CJ Haide (Ningbo) Biotech Co., Ltd is recalling Aminature L-Cysteine HCl Anhydrous due to a complaint of metal fragments.
NuVasive Inc is recalling 23 NVM5 EMG Modules because they contain an incorrect SSEP harness instead of the correct NVM5 Harness, potentially delaying spinal surgery monitoring.
Medtronic is recalling Accurian RF Ablation Cannulas because the probes may catch on a lip inside the hub, causing insertion difficulty.
Medtronic is recalling Accurian RF Ablation Cannulas because the probe catches on a lip inside the hub, causing insertion difficulty.
Medtronic is recalling Accurian RF Ablation Cannulas because the probe catches on a lip inside the hub, causing insertion difficulty.
Medtronic is recalling Accurian RF Ablation Cannulas because the probe may catch on a lip inside the hub, causing insertion difficulty.
Walker Emulsions Inc. is recalling Walker Hand Sanitizer because it contains DA-2I Ethanol, an excipient not approved for use in hand sanitizers.
Walker Emulsions Inc. is recalling 1-gallon bottles of 60% hand sanitizer because it contains an unapproved excipient, DA-2I Ethanol.
Medtronic is recalling Accurian RF Ablation Cannulas because the probe catches on a lip inside the hub, causing insertion difficulty.
LivaNova USA is recalling 140 sterile disposable connectors because some packages contained incorrect 3/8x1/4 reducers instead of the specified 1/2x1/2 connectors.
HF Acquisition Co. LLC is recalling specific lots of Famotidine Injection because a customer reported the product was received in a non-refrigerated state.
Triangle Tube is recalling about 63,000 Prestige Solo and Excellence gas boilers because a vent adapter may detach, causing carbon monoxide leaks. One death was reported.
BMW is recalling 2019-2020 X5 and 2020 X6 M vehicles because the steering column shaft bearing plate may not be properly attached, which can affect handling and increase crash risk.
Jamaican Tastee Patties, LLC is recalling approximately 60,457 pounds of beef and chicken patty products that were repackaged and relabeled without federal inspection.
Meritor is recalling specific pressure assemblies where an incorrect fitting may cause the power steering hydraulic hose to fail, resulting in a loss of steering assist.
Daimler Trucks North America is recalling 2021 Saf-T-Liner C2 School Buses because the brake pedal arm may rotate out of position, increasing crash risk.
High Altitude Trailer is recalling 2019-2020 XT50 trailers with retrofitted rear swing arm spare tire carriers because a weld may fail, causing the tire to separate and increasing crash risk.
Honda is recalling 2019-2020 Odyssey vehicles because water intrusion can cause the rearview camera to display a distorted or no image, increasing crash risk.
Honda is recalling 2018-2020 Odyssey vehicles because water in the door handle cables may cause freezing, preventing the sliding doors from latching securely.
Honda is recalling certain 2019-2021 Pilot vehicles due to faulty software that may prevent the rearview camera from displaying properly. This increases the risk of crashes since drivers cannot see behind the vehicle.
Tiffin is recalling 2018-2020 Zephyr and 2019-2020 Bus motorhomes because improperly wired control modules may cause windshield wipers to stop working.
Honda is recalling 2018-2020 Odyssey, 2019-2020 Passport, and 2019-2021 Pilot vehicles with software causing the instrument panel to fail to display critical information (engine oil pressure, speedometer, gear position) and preventing the rearview camera image from displaying.
Kia is recalling 2020 Telluride vehicles equipped with Smart Cruise Control because trailer brake lights may not illuminate when the system applies brakes, increasing crash risk.
Daimler Vans USA is recalling 2019 Mercedes-Benz Sprinter vans because the chassis may lack required stabilization, increasing crash risk.
Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because incorrect rear leaf spring shims may affect handling and increase crash risk.
PACCAR is recalling 2020 Peterbilt 520 trucks because incorrect bolts may allow the steering assist bracket to loosen, potentially locking the steering.
Coco's Italian Market is recalling approximately 16,868 pounds of frozen meat products produced without federal inspection. No adverse reactions have been reported.
Mercedes-Benz is recalling one 2020 GLE 350 because a driver's seat bolt may not be installed correctly, which could increase injury risk in a crash.
Great Dane is recalling 2018-2020 Truck Bodies because the license plate light may aim rearward, failing federal safety standards and increasing crash risk.
Kiel is recalling Avance coach seats because the automatic locking retractor mode of the seat belts cannot be activated, increasing injury risk in crashes.
Keystone Fuzion and Impact toy hauler travel trailers may have incorrectly wired generator transfer switches that could energize the shore power connection, creating an electrical shock hazard. Keystone will inspect and correct the wiring at no charge.
Polaris is recalling approximately 13,200 Ranger, PRO XD, and Bobcat utility vehicles because a defective clutch component can cause unexpected motion, posing a crash hazard.
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