Archive
478 recalls were announced in June 2020.
Of the 478 recalls this month scored against our rubric, 2% are Critical, 18% are Severe.
Which agencies issued them
Volvo is recalling specific 2007-2020 models because a front seat belt cable may fatigue and fail to secure occupants during a crash.
Bridgestone is recalling specific V-Steel tires for mobile cranes because they lack required DOT and safety markings, potentially leading to unsafe operating conditions.
BMW is recalling 2020-2021 7 Series vehicles because the rear middle child seat tether anchor may be inaccessible, increasing injury risk in crashes.
Pilgrim's Pride is recalling approximately 59,800 pounds of fully cooked chicken breast nuggets that may contain flexible rubber material.
Forest River is recalling 2021 Palomino Columbus recreational trailers because improperly located furnace vents may allow exhaust fumes to enter the trailer, posing a risk of carbon monoxide poisoning.
Forest River is recalling the 2021 Cherokee Wolf Pack toyhauler because the propane line may be routed around sharp edges, which can cause a leak and fire risk. Owners should contact Forest River at 1-260-499-2100 for a free repair.
Forest River is recalling 2020-2021 Rockwood trailers with incorrect Gross Axle Weight Rating information on their Federal Placards. This could allow operators to unknowingly overload the vehicle, increasing crash risk.
Chrysler is recalling 2020 Ram 1500 pickups and Promaster vans because a side curtain airbag diffuser may detach, preventing proper inflation in a crash.
FCA US LLC is recalling specific MOPAR steering drag link assemblies for Heavy Duty Ram 2500 and 3500 trucks because a jam nut may loosen, risking loss of steering control.
Tenneco is recalling Clevite-Pullman rear suspension lower control rods installed in Gillig Low Floor buses because the design makes them susceptible to failure over time.
Costway is recalling about 16,000 double baby strollers because they violate federal safety standards, posing fall, entrapment, and strangulation risks to children.
GE Healthcare is recalling Giraffe OmniBed infant incubators equipped with Servo Oxygen modules because they may deliver a different oxygen level than displayed.
SCA Pharmaceuticals is recalling 333 bags of Heparin Sodium 5,000 units due to out-of-specification potency results at the 30-day stability timepoint.
Toyota is recalling 2013-2015 Prius and 2014-2017 Prius V vehicles because excessive voltage in the inverter may cause the hybrid system to shut down, increasing crash risk.
Triple E is recalling 2020 Wonder W24MB, W24RTB, and W24FTB motorhomes because an improperly tightened electrical connection may short circuit and cause a fire.
Apotex Inc. is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above acceptable intake levels.
Defibtech is recalling 860 Lifeline PRO AEDs because a component issue may cause the device to abort or fail to deliver a shock.
Forest River is recalling 2020 Palomino Real-Lite campers because window glass may detach from the frame, posing a projectile hazard.
PD-Rx Pharmaceuticals is recalling specific lots of metformin HCL ER 500 mg tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
AvKARE Inc. is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Captain Rusty's Seafood Products LLC is recalling Lobster Dip because routine inspection found undeclared major allergens, including fish, egg, soy, milk, wheat, and crustacean shellfish.
Brake Parts Inc. is recalling aftermarket brake master cylinders for specific Volkswagen models because the piston may pop out, risking a complete loss of braking.
Stryker is recalling specific Humerus End Cap implants because the blister pack seal may be compromised, meaning sterility cannot be assured.
Captain Rusty's Seafood Products LLC is recalling Blue Crab Dip because it contains undeclared major allergens, including fish, egg, soy, milk, and wheat.
Siemens is recalling MAMMOMAT Revelation mammography systems because a software limitation may make it difficult to remove the vacuum biopsy system if an exam is interrupted.
Stryker GmbH is recalling specific locking screws because the blister pack seal may be compromised, meaning sterility cannot be assured.
Toyota is recalling 2019-2020 RAV4 and 2020 RAV4 Hybrid vehicles because water may enter the steering gear box, causing a loss of electric power steering assist.
Captain Rusty's Seafood Products LLC is recalling Smoked Mahi Dip because routine inspections found undeclared egg and soy allergens.
Becton Dickinson is voluntarily recalling Mueller Knife Handles because a machining burr on the collet threads may prevent the blade from seating securely.
Stryker is recalling specific lots of locking screws because the blister pack seal may be compromised, meaning sterility cannot be assured.
Abbott is recalling 421 Alinity C Processing Modules because they may generate incorrect results for specific chemistry assays.
The Furniture Connexion is recalling Modavari Forrest Live Edge Benches because they can tip over, posing fall and injury risks.
GE Healthcare is recalling Giraffe Incubators with Servo Oxygen modules because they may deliver different oxygen levels than displayed.
Stryker GmbH is recalling specific T2 Humerus End Cap implants because the blister pack seal may be compromised, meaning sterility cannot be assured.
Stryker is recalling specific lots of Locking Screws because the blister pack seal may be compromised, meaning sterility cannot be assured.
Stryker GmbH is recalling specific Advanced T2 Tibia Compression Screws because the blister pack seal integrity may be compromised, meaning sterility cannot be assured.
Stryker GmbH is recalling specific lots of Locking Screws because the blister pack seal may be compromised, meaning sterility cannot be assured.
Stryker is recalling specific locking screws because the packaging seal may be compromised, meaning sterility cannot be assured.
Resource Optimization & Innovation LLC is recalling Regard SRHS GIC Port A Cath devices because holes in the packaging may compromise the sterile field.
Stryker GmbH is recalling specific lots of locking screws because the blister pack seal may be compromised, meaning sterility cannot be assured.
Stryker GmbH is recalling specific lots of End Cap T2 Tibia implants because the blister pack seal may be compromised, meaning sterility cannot be assured.
Medtronic is recalling 36 units of Bone Void Filler, Small, because the product may not maintain its setting characteristics for the labeled shelf-life, potentially increasing surgical time.
Medtronic is recalling 41 units of Bone Void Filler Kits because the product may not set properly, potentially increasing surgical time and causing incomplete bone formation.
Stryker is recalling specific locking screws because the packaging seal may be compromised, meaning sterility cannot be assured.
Biomet is recalling 705 units of Screw Instrument Trays because the device and tray failed steam sterilization process validation testing.
Abaxis Inc is recalling 15 Piccolo Xpress chemistry analyzers because they display incorrect reference ranges for analytes, which may affect test result interpretation.
Biomet is recalling 136 units of the Outer Sheath 4.5/5.0,6.5 because the device and tray failed steam sterilization validation testing.
AvKARE Inc. is recalling Metformin Hydrochloride Extended-Release Tablets 750 mg because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Stryker GmbH is recalling specific lots of locking screws because blister pack seals may be compromised, potentially affecting sterility.
Stryker GmbH is recalling specific Gamma3 End Caps because the blister pack seal may be compromised, meaning sterility cannot be assured.
Defibtech is recalling 860 DDU-2300 AEDs because a component issue may cause the device to abort or fail to deliver a shock.
Captain Rusty's Seafood Products LLC is recalling Smoked Salmon Dip due to undeclared milk, a major allergen, discovered during a routine inspection.
Biosense Webster is recalling PENTARAY NAV High-Density Mapping Catheters because they can become entrapped in the heart's valves during use.
Captain Rusty's Seafood Products LLC is recalling Cajun Crab & Lobster Dip because it contains undeclared major allergens, including fish, egg, soy, milk, wheat, and crustacean shellfish.
Stryker GmbH is recalling specific End Cap implants because the blister pack seal may be compromised, meaning sterility cannot be assured.
Biosense Webster is recalling PENTARAY NAV High-Density Mapping Catheters because they can become entrapped in the cardiac valvular apparatus during use.
AngioDynamics is recalling BioFlo and Xcela PICC Convenience Kits because they contain BD PosiFlush SF Saline Flush Syringes that were previously recalled by BD Medical.
Vac-Tron is recalling 100 units of 2020 vacuum excavator trailers because they may be missing rear and rear-side reflex reflectors, which reduces visibility and increases crash risk.
Leica Microsystems is recalling ARveo and M530 OH6 microscope systems because voltage changes may cause equipment shutdown, potentially interrupting surgical procedures.
Defibtech is recalling 860 Lifeline ECG Automated External Defibrillators because a component issue may cause the device to abort or reset, potentially failing to deliver a shock.
Stryker GmbH is recalling specific lots of Locking Screws because the blister pack seal may be compromised, meaning sterility cannot be assured.
Medtronic is recalling 6 units of Bone Void Filler, Large, because the product may not maintain its setting characteristics for the labeled shelf-life.
GSK is recalling Gaviscon Regular Strength Liquid Antacid bottles because the labels lack a required magnesium safety warning.
Hikma Pharmaceuticals is recalling 82,426 vials of Irinotecan Hydrochloride Injection due to a crimp defect in the flip-cap.
Ortho-Clinical Diagnostics is recalling VITROS AMYL Slides Reagent because multiple coatings show imprecision on control fluids compared to expected standards.
Gaviscon Liquid Antacid Extra Strength is being recalled because the bottle label lacks a required magnesium safety warning. The recall covers single and twin-pack bottles distributed nationwide.
AngioDynamics is recalling certain PICC Kits because they contain BD PosiFlush SF Saline Flush Syringes that were previously recalled by BD Medical.
AngioDynamics is recalling BioFlo and Xcela PICC kits because they contain BD saline flush syringes that were previously recalled by BD Medical.
GSK is recalling Gaviscon Extra Strength Liquid Antacid because the bottle label is missing a required magnesium safety warning.
Eco Lips Inc. is recalling 68,400 tubes of EcoLips Sport Lip Balm, SPF 30, because the avobenzone concentration exceeds FDA limits.
Resource Optimization & Innovation LLC is recalling Regard SRHS Central Line Kits because holes in the packaging may compromise the sterile field.
Ortho-Clinical Diagnostics is recalling VITROS AMYL Slides Reagent because multiple coatings show imprecision on control fluids. The product is used for in vitro diagnostic testing.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Product Performance Verifier I units because multiple coatings of AMYL Slides show imprecision on control fluids.
Hikma Pharmaceuticals is recalling 17,998 vials of Irinotecan Hydrochloride Injection due to a crimp defect in the flip-cap.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Product Performance Verifier II units because multiple coatings of AMYL Slides show imprecision on control fluids.
Gaviscon Regular Strength Liquid Antacid is being recalled because the bottle label lacks the required magnesium safety warning.
AngioDynamics is recalling certain PICC Kits because they contain BD PosiFlush SF Saline Flush Syringes that were previously recalled by BD Medical.
Diasol, Inc. is recalling 212 cases of liquid acid concentrate for hemodialysis because of incorrect labeling of the dialysate concentration.
Aurobindo Pharma USA Inc. is recalling Olanzapine Tablets, USP 7.5 mg, because the product failed impurity and degradation specifications.
Volkswagen is recalling two 2018 Golf GTI vehicles because the VIN on the Federal Certification label may not match the actual vehicle VIN, potentially preventing owners from identifying safety recalls.
Abbott Vascular is recalling 13 units of Xience Sierra coronary stents because they bear an incorrect expiration date.
Aurobindo Pharma USA Inc. is recalling Olanzapine Tablets, USP 2.5 mg, because the product failed impurities and degradation specifications.
Newell is recalling 2020-2021 P50 motor coaches because a decorative cover may become lodged under the brake pedal, potentially impacting the ability to stop.
Ford is recalling 2020 F-250, F-350, and F-550 Super-Duty diesel pickups because a brittle transmission part may fracture, causing engine stalls or increased braking effort.
Ford is recalling 2020 Expedition and Lincoln Navigator vehicles because a driver's side second-row seat headrest bracket may be improperly welded, potentially failing to restrain occupants in a crash.
Mercedes-Benz is recalling 2020 C300, E350, and GLC300 vehicles because improperly tightened turbocharger oil line screws may cause leaks that increase fire risk.
ECCO is recalling 761 LED stop, tail, turn, and reverse lights for emergency vehicles because they may be too bright, potentially affecting other drivers' vision.
Forest River is recalling 2020 Surveyor trailers because a furnace may detach from the exhaust vent, creating a carbon monoxide hazard.
Grand Design is recalling 2016-2018 Reflection trailers because a wiring connector may allow water intrusion, potentially causing an electrical short circuit and fire.
The 2021 Forest River FR3 recreational vehicle has a wiring harness defect that can cause leveling jacks to deploy while driving, risking loss of vehicle control. Forest River will provide free repairs.
Certain 2020-2021 motorhomes built on Sprinter chassis may develop a brake hose chafed by the fender liner, potentially losing brake fluid. Owners should have dealers inspect and replace brake hoses and modify fender liners at no cost.
Lochinvar is recalling about 34,300 residential boilers because a flue grommet can fail, allowing carbon monoxide to escape. Consumers should contact a technician for a free repair.
Modus Furniture is recalling Brighton, Travis, and Bevelle dressers because they are unstable without mirrors, posing tip-over and entrapment risks to children.
American Honda is recalling about 25,000 2019-2020 Pioneer and Talon off-highway vehicles because they may move while in park, posing crash and injury risks.
Dometic is recalling specific CFX3 and CFF Series chest refrigerators because a faulty protection device may cause voltage overload, electrical damage, and fire risk.
Fresenius Kabi is recalling specific lots of Ketorolac Tromethamine Injection because particulate matter was found in reserve sample vials.
Endologix is recalling Ovation iX Abdominal Stent Graft Systems because a material weakness may cause polymer leaks during implantation, potentially leading to clinical events.
La Bodega Meat LLC is recalling approximately 83,038 pounds of raw beef products that were distributed without the benefit of import re-inspection.
Fresenius Kabi is recalling specific lots of Ketorolac Tromethamine Injection because particulate matter was found in reserve sample vials.
Arrow International is recalling FlexTip Plus Epidural Kits because a rotatable collar on the filter may detach, causing a leak.
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