Archive
391 recalls were announced in April 2022.
Of the 391 recalls this month scored against our rubric, 2% are Critical, 17% are Severe.
Which agencies issued them
Tiffin is recalling certain 2021 and 2022 Allegro and Allegro Bay motorhomes due to defective hydraulic cylinder seals. The slide-room may extend unintentionally, increasing crash risk.
Daimler Trucks North America is recalling 2019-2023 Thomas Built Buses HDX school buses because a battery cable may chafe and cause a fire.
Alliance RV is recalling certain 2022 Paradigm, Avenue, and Valor recreational trailers due to cracked quick disconnect fittings in the LP gas system that can cause gas leaks, creating a fire hazard.
About 635,000 Insignia air fryers and air fryer ovens can overheat, posing fire and burn hazards. Best Buy is offering refunds or store credit for affected units sold between November 2018 and February 2022.
MWA LLC is recalling about 4,200 LUXE+WILLOW heated blankets sold nationwide from January to March 2022 because the blanket can overheat if left plugged in and powered on for extended periods, creating fire and burn hazards.
Monti Kids is recalling about 1,375 Wooden Push Toys because the rolling cylinder can separate, exposing internal balls that pose a choking hazard to children. No injuries have been reported.
SafeRacks/Monsterrax overhead garage storage racks may collapse from the ceiling due to defective hex bolts, posing an impact injury hazard. About 12,800 units sold online from September through December 2021.
The Red League is recalling approximately 910 children's pajamas that fail to meet federal flammability standards for sleepwear, posing a risk of burn injuries. Consumers should remove the pajamas from children and contact The Red League for return instructions and a full refund.
Elite Comfort Solutions is recalling about 700 Nectar Premier Mattresses sold through nectarsleep.com from July to September 2021 because they fail to meet federal flammability standards, posing a fire hazard. No injuries have been reported.
Norwex USA is recalling approximately 40,000 ceramic knives because the handles can break during use, creating a laceration hazard. The knives were distributed free as promotional items from January through February 2022.
Sensory Medical Inc recalled 225 units of the Cub 2 Enclosed Bed Canopy System for potential misuse risk. The firm is updating product warnings and precautions for devices distributed before December 16, 2021.
Giant Eagle recalled Happy Face Cookies from two Ohio stores due to undeclared milk allergen. Consumers with milk allergies should not consume these products.
Kibbi, LLC is recalling 2021 Renegade Villagio and Vienna motorhomes because a stranded wire in the electrical relay may cause overheating and increase the risk of a fire.
Giant Eagle is recalling Happy Face Cookie 4-packs due to undeclared milk allergen. Consumers with milk allergies should avoid this product.
B&G Foods is recalling Back to Nature Cheddalicious Cheese Flavored Crackers due to undeclared egg and milk allergens caused by mispackaging. Consumers with egg or milk allergies should discard the product or return it.
Teva Pharmaceuticals is recalling IDArubicin Hydrochloride Injection vials due to the presence of silica and iron oxide particulate matter. The recall affects nationwide distribution within the United States.
Preferred Pharmaceuticals is recalling Clobetasol Propionate Lotion 0.05% distributed in Illinois due to manufacturing deviations and discontinued stability study program. Consumers should contact their healthcare provider.
Continental Mills is recalling Gordon Choice Southern Style Fish Breader (Lot KX2065) nationwide due to the presence of foreign materials. Consumers should not consume this product and should return it to the place of purchase.
Daimler Trucks North America is recalling 2022 Western Star 4900 and 4700 trucks because seat belts may not be secured properly, increasing injury risk in crashes.
BMW is recalling 2019-2023 X5, X6, X7, and 4 Series vehicles because the sunroof may close without the key fob inside, creating injury risk. Dealers will reprogram the control unit free of charge.
Continental Mills voluntarily recalls Krusteaz Cinnamon Crumb Cake (Lot KX2063) due to potential foreign materials that could pose a choking or injury risk.
Continental Mills is recalling Great Value Buttermilk Pancake & Waffle Mix (item #714-5000) due to foreign materials. Approximately 1,125 cases were distributed nationwide.
Krusteaz Buttermilk Pancake Mix (Lot code KX2066, best-by 3/6/2024) is being recalled nationwide due to foreign materials. Consumers should not consume this product.
Medline Industries is recalling approximately 8,990 cases of Standard PVC Laryngeal Masks distributed nationwide because the mask cuff may disconnect from the breathing tube.
Merit Medical is recalling AccessPLUS Large Bore Hemostasis Valves due to an internal design gap that can trap guidewires, potentially delaying medical procedures.
Stanbio Laboratory's Creamatocrit Plus breast milk analyzer was marketed without required FDA 510(k) clearance. Its performance has not been validated, and erroneous results could lead to inadequate nutritional supplementation for infants.
Kroger Buttermilk Pancake & Waffle Mix with specific lot codes may contain foreign materials. Consumers who purchased this product should not use it.
Continental Mills is recalling Gordon Choice Yellow Cake Mix (lot KX2066) nationwide due to the presence of foreign materials. The recall was voluntarily initiated on March 10, 2022.
Skippy Reduced Fat Creamy Peanut Butter (40 oz) is being recalled due to potential steel contamination. No illnesses have been reported.
Wilton Industries is recalling specific lots of Chocolate Cookie Bunny Hutch Kit because milk is not listed in the allergen statement, despite being present in the product.
Pepsico is recalling 780 cases of Lipton Iced Tea Peach 24-packs in four states due to incorrect labeling. Individual bottles labeled as zero sugar contain regular sugar.
Krusteaz Pro Buttermilk Pancake Mix is being recalled due to potential foreign materials. Approximately 970 cases with specific lot codes were distributed nationwide.
Skippy Foods recalls SKIPPY Creamy Peanut Butter Blended with Plant Protein (397g) due to potential small steel contaminants. The recall affects over 9,300 cases distributed across multiple states.
Skippy Foods recalls SKIPPY Reduced Fat Chunky Peanut Butter due to potential small steel contaminants. The recall affects 9,353 cases distributed across multiple U.S. states.
Taylor Farms is recalling Thai Noodle Salad Kit (108 oz) due to plexiglass found in an ingredient. The affected product was distributed to Kroger locations in Illinois, Indiana, Kentucky, Missouri, and Ohio with best by dates March 10-16, 2022.
Continental Mills is recalling 240 cases of IHOP Pancake Mix (Item #743-0278) nationwide due to the presence of foreign materials. Affected lots are KX2062 and KX2063 with a best-by date of 9/1/2022.
Preferred Pharmaceuticals is recalling certain lots of Lansoprazole Delayed-Release Capsules 15mg due to dissolution testing results that do not meet specifications. Approximately 791 bottles were distributed nationwide.
GE Healthcare's MUSE Cardiology Information System may lose test measurement edits and diagnosis statements after signing. The Class II recall affects 147 units in the US and internationally.
B Braun Medical Inc is recalling conductivity sensors used in Dialog hemodialysis systems due to potential cracking during use, which could cause leaks in the dialysate circuit and improper ultrafiltration. Affected patients should contact their healthcare provider.
Deerfield Imaging recalls the Trumpf Mount Clamp Assembly component used in surgical head fixation devices. The clamp may deflect during use and become difficult to loosen after procedures, potentially requiring surgical intervention.
LIPOSORBER LA-15 LDL Adsorption Column labeling has been updated to address a risk of severe anaphylactoid reactions and shock in patients receiving treatment while taking ACE inhibitors.
Boston Scientific is recalling ROTAWIRE Drive and ROTAWIRE Drive Floppy guide wire devices because pouch seals may be open, compromising sterility. The recall affects 433 5-packs distributed in the US, territories, Japan, and Canada.
Abbott Vascular is recalling INDEFLATOR Plus 30 balloon inflators due to increasing complaints of leaks and intermittent loose connections that could affect device function during medical procedures.
Luminex Corporation is recalling 4 Verigene Processor SP diagnostic devices that repeatedly failed to produce results, returning No Call outputs instead. Two of three customer complaints involved this malfunction.
Boston Scientific is recalling ROTAWIRE Drive guidewires due to potentially open pouch seals that could compromise product sterility. Affected units were distributed in the US, territories, Japan, and Canada.
Nextremity Solutions recalls the Nextra Hammertoe Correction System because the driver's proximal end is oversized, making it difficult to connect and remove from the implant, potentially delaying surgery.
Siemens Healthcare Diagnostics recalls approximately 2,158 units of Atellica CH Lithium_2 reagent (Lot Numbers 110108, 110185, 110238, 110302) due to potential for reagent carryover affecting quality control results, patient samples, and calibrator results.
The mounting brackets on Breas Ventilator Trolleys can become detached, allowing ventilators to fall. This poses an injury risk to people near the equipment.
Siemens Healthcare is recalling Atellica CH Hemoglobin A1c reagent kits due to potential reagent carryover affecting quality control and patient test results. The issue may cause inaccurate diabetes monitoring measurements.
Integra LifeSciences is recalling the Universal Flexible Arm (part number REF 1362275) because excess tightening force can break the internal cable at the tip, rendering the device unusable.
Graphic Controls' CLARAVUE Pre-wired Electrode set does not meet required electrical specifications for defibrillation use. The device fails to withstand 5,000 volts without breakdown, potentially resulting in ineffective defibrillation.
The Nextra Hammertoe Correction System surgical kit is being recalled due to an oversized driver that cannot properly connect to and remove from the implant. This defect can delay surgery.
CLARAVUE Pre-wired ECG electrodes may not meet electrical safety standards for defibrillation, potentially delivering an ineffective electrical charge during emergency use. This is a Class II recall affecting devices nationwide.
Graphic Controls' CLARAVUE Pre-wired Electrode units fail to meet electrical safety specifications required for defibrillation. The device delivers an inefficient electrical charge and may result in ineffective defibrillation.
Graphic Controls' CLARAVUE pediatric electrode set fails electrical safety standards. The device may not deliver adequate charge during defibrillation, potentially rendering emergency treatment ineffective.
Abbott Vascular is recalling 23 lots of Priority Pack accessory kits and packs due to reports of leaks and loose connections in the devices.
B Braun Medical Inc is recalling conductivity sensors used in Dialog and Dialog+ hemodialysis systems due to potential cracks that could cause dialysate circuit leaks, affecting ultrafiltration during treatment.
Abbott Vascular is recalling seven lots of the Plus 30 Priority Pack due to increased reports of leaks and intermittent loose connections in the vascular devices.
Conformis is recalling specific units of the iTotal Identity Posterior Stabilised Knee Replacement System due to incorrect tibial base plate implants being packaged in surgical kits.
Cardinal Health PROTEXIS PI and PI Classic surgical gloves were distributed without proper sterilization. The affected 486,578 pairs should not be used, as non-sterile gloves present an infection risk during surgical procedures.
Nextremity Solutions is recalling the Nextra Hammertoe Correction System Driver (SKU: NX-DR) due to oversizing at the proximal end, which impairs connection and removal from the implant, causing surgical delays. The defect affects 239 units distributed in the US, Japan, and the Netherlands.
Graphic Controls is recalling CLARAVUE Pre-wired Electrode sets because they fail to meet electrical safety specifications for defibrillators, potentially delivering inadequate charge during emergency treatment.
Abbott Vascular recalls 20/30 Indeflator medical devices due to increased complaints of leaks and loose connections. The recall affects 17 product lots distributed nationwide and internationally.
Nextremity Solutions is recalling the Nextra Hammertoe Correction System due to an oversized driver component that makes it difficult to properly connect and remove during surgery.
Nextremity Solutions recalls 459 units of the Nextra Hammertoe Correction System due to an oversized proximal driver end that prevents proper connection and removal during surgery.
The CLARAVUE Pre-wired Electrode does not meet electrical safety standards for defibrillators. It may not deliver effective electrical charge during emergency defibrillation.
Merit Medical Systems is recalling 36,445 Access-9 Large Bore Hemostasis Valves due to an internal gap that can trap the guidewire, potentially delaying medical procedures.
Siemens is recalling Atellica CH Calcium_2 diagnostic reagent due to potential reagent carryover that could impact quality control, patient samples, and calibrator results. The recall affects approximately 2,395 units distributed globally and in the US.
Varian ARIA radiation therapy management software versions 13.6 through 16.1 may generate incorrect treatment plan values that could direct radiation therapy to the wrong location. No illnesses have been reported.
Abbott Vascular is recalling the 20/30 Priority Pack w/COPILOT device due to an increase in complaints of leaks and loose connections. The recall affects 131 lots distributed nationwide and internationally.
Ittella International recalls Tattooed Chef Plant-Based Sausage Breakfast Bowls nationwide due to an incorrect gluten-free claim on the container lid. The product contains wheat flour, which is correctly listed in the ingredients and allergen statement.
Aurobindo Pharma USA Inc. is recalling 433,809 vials of Cyanocobalamin injection nationwide because assay testing showed the drug is subpotent, containing less than the specified 1,000 mcg/mL of active ingredient. Affected lots with specific expiration dates from September 2022 to April 2023 are identified for recall.
Bio-Botanica is recalling NATURE's ANSWER Coral Calcium supplements because the product contained cesium chloride, a New Dietary Ingredient. The recall affects 6852 bottles distributed to 17 states.
Preferred Pharmaceuticals is recalling Econazole Nitrate Cream 1% due to CGMP deviations. The manufacturer discontinued its stability study program; affected lots were distributed in California and Florida.
Medline Industries is recalling Stanbio TDM/Beta-Hydroxybutyrate Linearity Standards due to improper storage controls that may affect test result timing. The recall affects 10 boxes distributed to healthcare facilities in six states.
Continental Mills voluntarily recalled 450 cases of Krusteaz Belgian Waffle Mix nationwide due to the presence of foreign materials.
Medline's Hydroxybutyrate LiquiColor Tests are recalled due to improper storage that may cause delayed test results. The recall affects 45 units distributed across 16 U.S. states.
Siemens Healthcare Diagnostics is recalling Atellica CH Fructosamine reagent (lots 211359, 211451) due to potential reagent carryover that could affect diagnostic test accuracy.
Philips is updating instructions for cleaning and disinfecting reusable autoclavable temperature probes due to revisions needed in the disinfection process.
Volcano Corp is recalling MM-TSM touch screen modules used with IntraSight Integrated IVUS systems because they may crack or become damaged, potentially rendering the imaging equipment non-functional.
IntraSight Mobile IVUS Systems touch screen modules lack required labeling information including device identifier and manufacturer information. Affected units were distributed to healthcare facilities in the US and internationally.
Enerco is recalling specific Mr. Heater LP gas quick connector fittings because they may crack and leak gas, increasing the risk of fire.
Maserati is recalling 2022 MC20 vehicles because faulty rear tail lights may cause brake lights to flicker, potentially confusing other drivers and increasing crash risk.
Triple E Recreational Vehicles is recalling 2021-2022 Wonder W24RL models because an incorrect weight decal may lead to overloading the storage compartment.
Tesla is recalling one 2022 Model X vehicle due to a missing body structure reinforcement bracket at the second-row seat. This failure to comply with federal seat restraint standards increases the risk of occupant injury in a crash.
Tesla is recalling certain 2018-2022 Model 3 Performance vehicles because the speedometer's mph/km/h unit display may fail in Track Mode. Drivers may not know their vehicle's speed, increasing crash risk. Tesla will provide a free software update.
Firehouse Jams is recalling 3,819 pounds of uncured bacon marmalade produced without federal inspection. No adverse reactions have been reported.
Tiny Idahomes is recalling 2021-2022 Rugged Mountain Custom RV Travel trailers because an improperly welded coupler may cause the trailer to separate from the tow vehicle.
Mercedes-Benz is recalling certain 2021 GLC models because the headlight electrical connection may not be watertight, risking headlight failure. Reduced visibility increases crash risk.
Autocar is recalling 2019-2021 Xpeditor vehicles because the hazard lights do not function when the ignition is off, increasing crash risk. Dealers will repair or replace the wire harness at no charge.
General Motors is recalling 2015 Buick Enclave, Chevrolet Traverse, and GMC Acadia vehicles because the driver's air bag inflator may explode during deployment.
Ford is recalling 2015 Escape vehicles with 2.0L engines because a shifter cable bushing may degrade or detach, potentially causing unexpected vehicle movement or rolling.
GE Appliances is recalling about 155,000 French door refrigerators because the freezer handle can detach when opened, posing a fall hazard. The company has received 71 reports of handle detachment resulting in 37 injuries, including three serious falls.
Bentley is recalling 2021-2022 Bentayga vehicles because second row seats may not be locked on all rails, increasing injury risk in a crash.
Ford is recalling specific 2020-2022 Explorer models because a rear axle bolt may fracture, causing the driveshaft to disconnect and increasing crash risk.
Nissan is recalling certain 2022 Rogue vehicles due to a manufacturing defect that may cause fuel tank walls to be too thin. Road debris could puncture the tank, creating a fire hazard.
Ford is recalling 2020 Super Duty trucks with 6.7L diesel engines because a transmission washer can disintegrate, potentially preventing the vehicle from holding Park.
Ford is recalling 2020-2021 F-150s, Expeditions, Super Duties, and Lincoln Navigators with defective windshield wiper arms that may break and fail, reducing visibility and increasing crash risk. Owners should contact Ford at 1-866-436-7332 to schedule a free replacement.
Chrysler is recalling 2022 Jeep Grand Cherokee vehicles because a software error prevents the driver from knowing if a turn signal fails, increasing crash risk.
Rae Wellness has recalled approximately 191,200 units of Prenatal and Immunity Capsules because the bottles do not have child-resistant packaging as required by law. The iron-containing supplements pose a risk of poisoning if swallowed by young children.
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