Archive
561 recalls were announced in July 2022.
Of the 561 recalls this month scored against our rubric, 1% are Critical, 17% are Severe.
Which agencies issued them
Queen Bee Gardens recalls Honey Caramels Vanilla products that may contain undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts), which can harm consumers with allergies.
Chuckanut Bay Foods is recalling Chocolate Cheesecake Bites because the label lists Sunflower Lecithin when the product actually contains Soy Lecithin, an undeclared allergen. Consumers with soy allergies face a potential health risk.
Revive Superfoods Strawberry Zen smoothie mix is being recalled due to potential norovirus contamination in IQF raspberries used as an ingredient. The recall affects 57,960 units distributed to consumers in Pennsylvania, California, Illinois, and Texas.
Queen Bee Gardens is recalling Dark Raspberry Classic snacks due to undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts) that may be present, posing a risk to consumers with tree nut allergies.
Queen Bee Gardens is recalling Bee Joyful Bars due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. The product poses a health risk to consumers with tree nut allergies.
Queen Bee Gardens is recalling Midnight Gold Classic Truffles for potentially containing undeclared tree nuts, which pose a risk to allergic consumers. Distribution included Colorado, New Mexico, Wyoming, and nationwide online.
Queen Bee Gardens is recalling Honey Caramels Red Raspberry because the product may contain undeclared tree nuts. The recalled items were distributed to Queen Bee retail stores in Colorado, New Mexico, and Wyoming, and nationwide via internet sales.
Queen Bee Gardens recalls Truffle Dark Gift Box due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. The product poses a risk to consumers with tree nut allergies.
Queen Bee Gardens is recalling Huckleberry Truffles because they may contain undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). Products were sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide via internet.
Chuckanut Bay Foods is recalling Dipped Cheesecake Bites Chocolate because the product label lists Sunflower Lecithin when it actually contains undeclared Soy Lecithin, a potential allergen.
Stryker Neurovascular is recalling 71 Trevo Trak 21 Microcatheter units because the product carton label is missing the required product drawing or illustration.
Randox Laboratories is recalling Soluble Transferrin Receptors Calibrator kits used in lab analyzers. The calibrators can produce incorrect test results, with some values potentially underestimated by up to 30 percent.
Glenmark Pharmaceuticals is recalling Aspirin and Extended-Release Dipyridamole Capsules due to capsule breakage defects. Approximately 168,936 bottles were distributed nationwide.
Stryker is updating the Instructions for Use for the Triton Sponge System software (versions 4.6.5, 4.8.7, 4.9.6) to clarify proper handling technique for sponges and calibration placard. The FDA Class III recall affects 51 units distributed nationwide.
Randox Laboratories is recalling Soluble Transferrin Receptor reagent (TF10159) due to calibration curve defects causing inaccurate test results on Siemens Atellica CH analyzers.
LumiraDx is recalling SARS-CoV-2 antibody quality control products because modifications to the test were made outside the scope of FDA-approved authorization. The recall affects 99 units distributed across 13 U.S. states.
Launch Sequence Euphoria Capsules were marketed without FDA approval. Consumers should discontinue use immediately and contact the manufacturer.
Vi-Jon's hydrogen peroxide topical solution has been recalled due to cross-contamination with low levels of isopropyl alcohol. Multiple brands are affected nationwide in the USA and Canada.
Xstrahl Limited is recalling specific lot codes of the X80 RADiant Photoelectric Therapy System due to a potential compatibility issue with replacement treatment applicators. Devices were distributed in Florida, California, and Kentucky.
Boston Scientific is recalling GreenLight HPSEA Laser Fibers due to an incompatibility with the fiber card that causes an error message and requires equipment replacement during procedures.
Synapse Biomedical revised labeling for the NeuRx Diaphragm Pacing System to clarify that temperature range symbols indicate storage conditions, not transport or package conditions. The revision affects 71 units distributed in the United States.
R & D Systems is replacing Instructions for Use (IFU) for Quantikine IVD Erythropoietin Human Serum Controls due to an incorrect CE marking designation that should not appear on the self-certified product.
Ferrari is recalling various models from 2005-2022 because a defective brake fluid reservoir cap may cause a leak, leading to partial or total loss of brake function.
Capacity of Texas is recalling 2021-2022 TJ 5000, 6500, and 9000 trucks because incorrectly assembled steering gears may fracture, causing loss of steering control.
Spartan Fire is recalling 2020-2021 Metrostar and Gladiator fire trucks because a loose electrical connection may cause the load center to overheat and increase the risk of a fire.
E-One is recalling specific 2019-2022 fire trucks because a loose electrical connection may cause the load center to overheat, increasing fire risk.
Ford is recalling certain 2022 F-53 and F-59 motorhome and commercial chassis vehicles because the steering wheel attachment bolt may loosen and separate. This could result in loss of steering control and increased crash risk.
Ember is recalling 2022 Overland series trailers because cracked LP gas fittings may cause a leak, increasing the risk of fire.
Lion Electric is recalling 2020-2022 Lion C school buses because the parking brake may fail if not properly adjusted, increasing crash risk.
Shyft Group is recalling certain 2022-2023 Spartan RV Chassis vehicles due to improperly assembled steering gears that may fracture, causing loss of steering control. Owners should contact the manufacturer for free inspection and replacement.
Monroe Towmaster is recalling 2021-2022 TC-14D, T-24, and TC-24 trailers because installed tires have a lower load rating than required, increasing the risk of tire failure and crashes.
Daimler Trucks North America is recalling 2019-2023 Thomas Built Buses Minotour school buses because tire labels list the wrong size, potentially affecting vehicle stability.
Mercedes-Benz has recalled certain 2019–2022 AMG vehicles (CLS53, E53, GT53, and GT43 models) due to transmission wiring harness misrouting that can expose electrical connectors to corrosion, creating a fire risk.
Jaguar Land Rover is recalling certain 2022-2023 Land Rover Defender and other models due to defective front seat belt pretensioners that may fail to properly restrain occupants in a crash, increasing injury risk.
Cheetah Chassis is recalling 2023 trailers because twist lock handles may separate, creating a road hazard or unsecuring containers.
Aqualung i330R SCUBA diving computers can fail to adjust for user altitude and display incorrect dive-time calculations above 3,000 feet, creating risks of decompression sickness and drowning.
Vichy Laboratoires is recalling LiftActiv Peptide-C Anti-Aging Ampoules because the glass vials can break when opened, causing cuts to fingers and hands. The manufacturer has received 35 injury reports, including one requiring stitches.
Tesla is recalling certain 2022 Model S vehicles because the front bumper carrier structure may alter crash detection, causing the front passenger airbag to deploy incorrectly during low speed crashes. This increases the risk of passenger injury.
Toyota is recalling certain 2022-2023 Tacoma vehicles due to insufficient welds in the upper child seat anchors. These defects may prevent proper anchoring of child seats, increasing the risk of injury during crashes or sudden stops.
Nissan recalls 2022 Pathfinder rental vehicles where a software defect can disable the rearview camera, increasing crash risk. Affected customers will receive a free software update via dealer or over-the-air update.
The Hammock Source is recalling about 32,500 Key West Knock Down Hammock Stands because the weld attaching the stand to the base can break, posing a fall hazard. Nine reports of stands breaking have been received, including two reports of scrapes and bruises.
Subaru recalls 2015-2021 WRX vehicles; backup light switch may corrode and fail, disabling backup lights and rearview camera in reverse, reducing visibility and increasing crash risk.
Jaguar is recalling 2021-2022 F-PACE vehicles because incorrect tail lights may cause rear turn signals to fail, increasing crash risk.
Toyota is recalling 2022 RAV4, RAV4 Hybrid, and RAV4 Prime vehicles because a front passenger seat occupant detection sensor may fail to properly detect occupants. This could cause improper air bag deployment during a crash, increasing injury risk.
Jaguar is recalling 2022 XF, F-Type, and F-Pace vehicles because the driver and front passenger seat belt pretensioners may be damaged, causing improper restraint during a crash.
Monti Kids is recalling about 1,500 Toy Box with Bins units sold online from July 2021 through February 2022 because a small dowel can become exposed and detach, posing a choking hazard to young children.
Crye Precision is recalling LRB Leg Loops because the buckle can loosen and slip when worn with a load-rated belt, creating a fall hazard. About 300 units are affected.
Cruiser RV is recalling 2022 Shadow Cruiser travel trailers because the federal certification label displays the incorrect Gross Axle Weight Rating, which may allow the vehicle to be overloaded.
Konges Sløjd Baby Mirror Activity Toys are being recalled because the mirror can detach from the silicone cover, exposing sharp edges that pose a laceration risk to children. About 85 units were sold in the United States.
Bryant Ranch Prepack has recalled Morphine Sulfate extended-release tablets due to a label mix-up where bottles may contain the wrong strength. Contact your pharmacy to verify your correct dose.
Arti King Refozado con Ortiga y Omega 3 Tablets are recalled nationwide because FDA testing found undeclared diclofenac and dexamethasone. The product was marketed without FDA approval and should not be used.
Natreve Vegan Protein Powder (Lot# 46359 and 46360) is recalled nationwide due to an undeclared milk allergen.
Wawa cold brew coffee pints are being recalled due to undeclared peanuts. Approximately 1,000 units were distributed in Delaware, Florida, Maryland, New Jersey, Pennsylvania, Virginia, and Washington DC.
Zeltiq Aesthetics is voluntarily recalling CoolCurve+ ZELTIQ Vacuum Applicators due to increased reports of Paradoxical Hyperplasia during 2019–2021, an adverse event involving abnormal fat growth at treatment sites.
MSI Express Inc. is recalling Knorr Curry Chicken and Rice Soup Mix because it contains undeclared milk, a known allergen.
Morphine Sulfate extended-release tablets (30 mg) distributed in Alabama were recalled due to a critical label mix-up where bottles labeled as 60 mg contain 30 mg, and bottles labeled as 30 mg may contain 60 mg.
J & M Foods is recalling Favorite Day Lavender Shortbread Cookie Bites for undeclared egg and soy lecithin. Consumers with allergies to these ingredients should not consume the product.
Tailor Made Compounding is recalling 106 vials of compounded testosterone/anastrozole injectable due to lack of sterility assurance. The product was distributed nationwide in the USA and Puerto Rico.
Daimler Trucks North America is recalling 2023 Thomas Built Buses Saf-T-Liner EFX school buses because they may lack sufficient emergency exits, increasing injury risk during emergencies.
Volkswagen is recalling certain 2021-2022 Atlas Cross Sport vehicles due to an infotainment system defect that may prevent the rearview camera image from displaying. This loss of rear visibility increases crash risk.
Tiffin is recalling certain 2021-2023 Allegro and related motorhomes due to a defective LPG tank connection that may cause propane leaks and fire risk. Free inspection and repair are available through Tiffin dealers.
Volkswagen is recalling certain 2019-2021 Audi Q8 and 2020-2021 Audi Q7 vehicles due to a fuel pump component that may break, causing the pump to fail. A failed fuel pump can stall the engine, increasing crash risk.
BMW is recalling 2022 X3 xDrive30i vehicles because the high-pressure fuel rail may crack and cause a fuel leak in the engine compartment, increasing the risk of fire. Dealers will replace the fuel rail free of charge.
Tailor Made Compounding recalls 39 vials of a compounded injectable product for lack of assurance of sterility. Distribution was nationwide in the USA and Puerto Rico.
Volkswagen Group of America is recalling 2,584 2022 Audi A3 and S3 sedans because the seat belt tensioners may not restrain occupants properly during a crash.
Alliance RV is recalling 2022-2023 Paradigm and Valor travel trailers due to electric retractable awning weld separation that may allow the awning to drop unexpectedly, increasing injury risk.
Tailor Made Compounding recalls 84 vials of Dexpanthenol Preservative Free due to lack of assurance of sterility. The medication was distributed nationwide and in Puerto Rico.
Alcon has recalled 320 kits of Custom Pak Surgical Procedure Packs distributed across Arizona, California, Missouri, and New York because they contain latex gloves instead of the specified non-latex gloves, creating an allergen hazard for sensitive patients.
Fruselva America SPA is recalling Nature's Promise Organic Mango, Banana, Kale, Rice & Pineapple baby food pouches due to elevated thallium (heavy metal) contamination. Affected products were distributed in MA, ME, NH, NY, VT, MD, PA, and WV.
Tailor Made Compounding is recalling 63 vials of Hydroxocobalamin 25mg/mL injectable solution nationwide due to lack of assurance of sterility. Consumers should not use affected batches.
Aesculap Implant Systems LLC is recalling TC Cooely Micro Needleholder instruments because units labeled as 200mm are actually 150mm. This labeling error could impact surgical procedures.
AquaBplus 2000 water purification systems for dialysis have an installation guideline error that may reduce heat disinfection effectiveness. Patients using affected units may be at risk.
Medtronic MiniMed 620G insulin pumps may experience battery cap deterioration, resulting in incomplete battery circuit and loss of power. Approximately 2,287 affected pumps have been distributed across the U.S.
Tailor Made Compounding recalls 101 vials of Glycyrrhizic Acid (8mg/mL) nationwide due to lack of assurance of sterility in this injectable preparation. Patients should contact their healthcare provider.
Market Day Krabbycakes (840 bags, Item 3320) are being recalled because they contain undeclared shrimp and carmine colorant. The product was distributed across multiple states; consumers with shellfish allergies should not consume it.
Walker & Sons Inc is recalling Slap Ya Mama Cajun Fish Fry due to undeclared wheat allergen. Consumers with wheat allergies should not consume the product.
Tailor Made Compounding is recalling 90 vials of GAC (Glutamine/Arginine/L-Carnitine) injectable solution distributed nationwide and in Puerto Rico due to lack of assurance of sterility.
Tailor Made Compounding recalls 349 vials of Estradiol Cypionate 10mg/mL due to lack of assurance of sterility. The product was distributed nationwide in the USA and Puerto Rico.
Tailor Made Compounding is recalling 220 vials of Pentosan Polysulfate Sodium due to lack of assurance of sterility. The affected batches were distributed nationwide in the United States and Puerto Rico.
Tailor Made Compounding recalled 9,993 vials of compounded semaglutide/cyanocobalamin due to lack of assurance of sterility. No illnesses have been reported.
Jubilant Draximage Inc. is recalling Draximage MAA, an injectable diagnostic drug kit, due to failed endotoxin testing. The recall affects 519 cartons distributed nationwide (Lot 1H005, expiration November 30, 2023).
Tailor Made Compounding recalls two batches of Alprostadil/Papaverine/Phentolamine injectable due to lack of sterility assurance. The recall affects 32 vials distributed nationwide and in Puerto Rico.
Tailor Made Compounding is recalling 924 vials of Methionine/Inositol/Choline B12 + Carnitine injectable compound nationwide due to lack of assurance of sterility.
TMC Acquisition LLC is recalling Alpha Lipoic Acid 25mg/mL vials due to lack of assurance of sterility in manufacturing. The product was distributed nationwide.
TMC Acquisition LLC is recalling Folic Acid 5mg/mL injectable vials due to lack of assurance of sterility. The recall affects 45 units distributed nationwide and in Puerto Rico.
Tailor Made Compounding is recalling 652 vials of Methylcobalamin 10mg/mL injectable due to lack of assurance of sterility. No illnesses or injuries have been reported.
Tailor Made Compounding is recalling 243 vials of Nandrolone Decanoate injectable medication due to lack of sterility assurance. The affected product was distributed nationwide in the USA and Puerto Rico.
Tailor Made Compounding recalls Testosterone Cypionate injections due to lack of sterility assurance. The recall affects 4,219 vials distributed nationwide.
Tailor Made Compounding is recalling 294 vials of Gonadorelin 100mcg/mL distributed nationwide because the manufacturer cannot assure the product meets sterility standards.
Tailor Made Compounding recalls Glutathione 200mg/mL injectable vials due to lack of sterility assurance. The FDA Class II recall affects 40 vials distributed nationwide.
Tailor Made Compounding has recalled Vitamin D3 50,000IU/mL vials nationwide due to lack of sterility assurance during manufacturing. No illnesses have been reported.
Tailor Made Compounding is recalling Levocarnitine 500mg/mL vials nationwide due to lack of sterility assurance, a Class II FDA recall.
TMC Acquisition LLC recalls 191 vials of Methylcobalamin 1mg/mL distributed nationwide and in Puerto Rico due to lack of sterility assurance. Consult your healthcare provider regarding any vials in your possession.
Tailor Made Compounding is recalling 176 vials of testosterone cypionate/propionate injectable due to lack of assurance of sterility. The product was distributed nationwide.
Tailor Made Compounding has recalled 182 vials of Melanotan I injectable due to lack of assurance of sterility. The affected vials were distributed nationwide and in Puerto Rico.
Tailor Made Compounding is recalling 5,842 vials of compounded semaglutide/cyanocobalamin injectable due to lack of sterility assurance. The product was distributed nationwide in the United States and Puerto Rico.
Tailor Made Compounding is recalling Teriparatide injectable syringes nationwide due to lack of assurance of sterility. Patients using affected batches should contact their healthcare provider immediately.
Tailor Made Compounding is recalling ascorbic acid injectable vials due to lack of sterility assurance. The affected vials were distributed nationwide and in Puerto Rico.
Tailor Made Compounding is recalling 246 vials of compounded testosterone injections distributed nationwide due to lack of assurance of sterility. Non-sterile injectable medications may pose a risk of infection.
Tailor Made Compounding is recalling 1,562 vials of Sermorelin/Glycine injectable distributed nationwide because the manufacturer cannot assure the product meets sterility standards. Patients should stop using the recalled product and contact their healthcare provider.
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