Archive
857 recalls were announced in June 2022.
Of the 857 recalls this month scored against our rubric, 3% are Critical, 27% are Severe.
Which agencies issued them
Cargill Cocoa and Chocolate Inc is recalling 795 boxes of Milk Chocolate Covered Peanut Butter Eggs due to possible Salmonella contamination. The product was distributed to consumers in multiple states.
Euphoria Trading Company is recalling Milk Chocolate Peanut Butter Meltaways due to potential Salmonella contamination in the Jif peanut butter ingredient. The recall is classified as FDA Class I.
Cargill Cocoa and Chocolate Inc is recalling Dark Chocolate Covered Peanut Butter Meltaways due to possible Salmonella contamination. Affected boxes with lot codes 220224AA, 220219AB, and 220215AC were distributed to consumers in multiple states.
Butter Buds Inc voluntarily recalled Butter Buds 8X Non-Dairy food ingredient due to undeclared milk, which poses a risk to consumers with milk allergies. The product was distributed in seven U.S. states and internationally.
Blue Moose of Boulder, LLC is recalling Blue Moose Spinach Artichoke Parmesan Dip because it contains cashews and soy, which are not listed on the label. Consumers with allergies to these ingredients face serious health risks.
Indianapolis Fruit Company recalls Garden Cut Apple Tart for potential Salmonella contamination in peanut butter. Distributed in Kentucky, Illinois, Indiana, Michigan, Ohio, West Virginia, and Wisconsin.
Deskins Candies Peanut Butter No Bake candies are recalled due to Salmonella contamination in the peanut butter. The recall affects 167 cases distributed in West Virginia, Virginia, and North Carolina.
Garden Cut Celery Bites w/ Peanut Butter may contain Salmonella in the peanut butter component. Affected 6oz packages were distributed in seven states with Best By dates between May 25 and June 3, 2022.
Cargill Cocoa and Chocolate Inc is recalling Peanut Butter Fudge due to possible Salmonella contamination. Lot 220219AC with Best if Used by Date 4/19/2022 was distributed across multiple states.
Cargill Cocoa and Chocolate Inc is recalling 795 boxes of Milk Chocolate Covered Peanut Butter Meltaways due to possible Salmonella contamination. The affected product was distributed to retail locations and consumers in multiple states.
Deskins Candies Peanut Butter Fudge is being recalled due to Salmonella contamination in the peanut butter ingredient. The recall affects products distributed to West Virginia, Virginia, and North Carolina.
Deskins Wholesale, LLC is recalling 181 cases of Deskins Candies Peanut Butter Pinwheel due to Salmonella contamination in the peanut butter component. The affected product was distributed in West Virginia, Virginia, and North Carolina.
Cargill Cocoa and Chocolate Inc is recalling Milk Chocolate Covered Peanut Butter Ritz Crackers due to possible Salmonella contamination. Affected lots were distributed across multiple states.
Dexter Axle is recalling 42mm Cartridge Bearing Washers that may crack and cause the hub to separate from the axle, increasing the risk of a crash.
Draeger Medical is recalling approximately 35,950 Drager SafeStar 55 medical devices due to a manufacturing error that may cause occlusion of the device's filters, potentially preventing proper device function.
Artri King Reforzado con Ortiga Omega 3 Tablets are being recalled for containing undeclared diclofenac and being marketed without FDA approval. The recall affects 1,308 bottles distributed nationwide.
Euphoria Trading Company is recalling Dark Chocolate Peanut Butter Meltaways distributed in Oregon due to potential Salmonella contamination from Jif peanut butter.
A G Specialty Foods Inc recalls We BE PB & Jammin Snack Boxes (6 oz) sold in Oregon and Washington due to potential Salmonella contamination.
A G Specialty Foods Inc is recalling Peanut Butter Strawberry Jam Old Fashioned White Bread due to potential Salmonella contamination. Affected products were distributed in Oregon and Washington with best-by dates from May 16 to June 3, 2022.
Cargill is recalling 795 boxes of Dark Chocolate Covered Peanut Butter Eggs (Item code K119D) due to possible Salmonella contamination. Products were distributed to consumers across multiple states.
Indianapolis Fruit Company is recalling Garden Cut Apples with Peanut Butter because the peanut butter component may be contaminated with Salmonella. The recall affects 118 cases distributed to seven U.S. states.
A G Specialty Foods Inc is recalling Peanut Butter Strawberry Jam White Bread due to potential Salmonella contamination. Affected products were distributed in Oregon and Washington.
Taylor Farms New Jersey is recalling Wawa Apples & Peanut Butter 4.9oz. snacks due to possible Salmonella contamination. Products were distributed to Wawa locations in DC, DE, FL, MD, PA, NJ, and VA.
A G Specialty Foods Inc is recalling The Goods Snack Pack due to potential Salmonella contamination. The affected products have Best if Used By dates from 05/16/2022 through 06/03/2022 and were distributed in Oregon and Washington.
Morski Brands is recalling Marketside Gouda Bacon Green Chile Dip distributed nationwide by Walmart due to potential metal fragments in the product. Consumers should not consume affected units.
Morski Brands recalled 832 units of Dawn's Smoked Gouda & Bacon Potato Salad due to possible metal fragments. Consumers with products bearing best-before dates 5-13-22, 6-21-22, 6-24-22, or 6-27-22 should not consume them.
Cedar Crest Caramel Collision Ice Cream is being recalled due to the presence of plastic foreign material in the product. The affected product was distributed across IL, MI, MN, TX, and WI.
Cedar Crest Specialties, Inc. is recalling Cedar Crest WI Campfire S'Mores Ice Cream due to foreign plastic material in the product. Consumers should not consume the affected product.
Morski Brands recalls Ranch BLT Pasta Salad nationwide due to possible metal fragments. The product was sold under Finest Traditions and Dawn's brands with a best-before date of 6-13-22.
Micro Therapeutics is recalling Axium Detachable Coil Systems due to incorrect size and configuration labeling. The 96 affected units were distributed to China and the Republic of Korea.
Thistle Health Inc. recalls 1,003 bottles of Thistle Tropical Limeade due to strawberries potentially contaminated with Hepatitis A. Affected product was distributed in California, Nevada, Oregon, and Washington.
Morski Brands, Inc. is recalling 2,648 units of Finest Traditions Smokey Baked Beans due to the potential presence of foreign metal objects. The recalled product was distributed nationwide.
Morski Brands recalls 1,312 units of Dawn's Campfire BBQ Beans nationwide due to metal foreign objects. Consumers should not consume the product.
Sun Pharmaceutical is recalling medroxyprogesterone acetate injectable suspension due to lack of assurance of sterility. The recall affects approximately 57,997 prefilled syringes distributed nationwide.
Abbott Laboratories recalls one lot of Pedialyte Strawberry Lemonade powder because dextrose derived from wheat was not declared on the label. Lot code 287112S00.
The emergency braking system on certain 2022 Freightliner Cascadia trucks may fail to engage, creating a risk of brake failure. Dealers will install a corrective valve at no cost.
Grand Design is recalling 165 model-year 2022 Momentum travel trailers due to improper 110-volt electrical wiring that can overheat and create a fire risk. Dealers will rewire the power supply at no cost.
Daimler Trucks North America is recalling 2023 Thomas Built Saf-T-Liner C2 school buses because they may lack sufficient emergency exits, increasing injury risk during emergencies.
Tandem t:slim X2 insulin pumps may display inaccurate battery levels, risking insulin delivery failure if the battery depletes unexpectedly. Users should maintain battery above 25% to prevent unintended insulin cessation.
GE Healthcare is recalling CARESCAPE Central Station V2 patient monitoring devices due to potential power supply failure that can cause device shutdown and loss of patient monitoring.
Olympus URETERO-RENO FIBERSCOPE Model URF-P6R recalled due to incorrect adhesive securing the diopter ring, which may cause loss of focus and in rare cases urinary tract perforation.
Washington Homeopathic Products is recalling Proteus homeopathic remedy in multiple potencies due to manufacturing process deviations. The firm initiated this voluntary recall in May 2022.
Sun Pharmaceutical is recalling medroxyprogesterone acetate injectable suspension (150 mg/mL) nationwide due to lack of assurance of sterility. Affected lots contain vials with expiration dates from December 2022 through September 2023.
Sun Pharmaceutical is recalling 4,625 syringes of Medroxyprogesterone Acetate Injectable Suspension (Lot HAC1951A) due to lack of assurance of sterility. The affected medication was distributed nationwide.
Lupin Pharmaceuticals is recalling Zileuton Extended-Release Tablets, 600 mg, due to failed dissolution specifications found during stability testing that may affect medication efficacy.
Sun Pharmaceutical is recalling 26,892 vials of medroxyprogesterone acetate injectable suspension (150 mg/mL) distributed nationwide due to lack of assurance of sterility. The affected lots expire between January and June 2023.
White Cane Sockeye Salmon packages contain undeclared wheat and soy in the teriyaki sauce. Consumers with allergies to these allergens should not consume this product.
RoRo's Dinn-A-Rolls (10oz, UPC 86945900031) are being recalled because the label fails to declare milk as a sub-ingredient in butter. Consumers with milk allergies should not consume this product.
Morski Brands is recalling Steakhouse Potato Salad products nationwide due to metal contamination. Affected brands include Finest Traditions and Dawn's.
Thistle Health Inc is recalling Thistle Watermelon Berry Cold-Pressed Organic Juice (32 fl oz) due to potential Hepatitis A contamination in the strawberry ingredient. The recall affects 965 bottles distributed in California, Nevada, Oregon, and Washington.
Soul Cedar Farm's Zesty Sweet Peppers are being recalled due to potential contamination with Clostridium botulinum. Testing found a pH level of 5.57, which can support dangerous pathogen growth in shelf-stable foods.
Medtronic is recalling Cobalt and Crome ICDs and CRT-Ds due to a software telemetry error in the CareLink SmartSync Device Manager. The error may affect device communication and remote monitoring.
Illumina is recalling approximately 1,014 MiSeq Dx sequencing instruments due to a cybersecurity vulnerability. The devices are distributed worldwide and throughout the United States.
Illumina is recalling 799 NextSeq 550 Dx genetic sequencers due to a cybersecurity vulnerability in the Local Run Manager software. Affected devices have been distributed worldwide and in the United States.
Olympus endoscopes with defective diopter ring adhesive may cause vision loss and, in rare cases, urinary tract perforation.
The Olympus URETERO-RENO FIBERSCOPE Model URF-P6 is recalled for incorrect adhesive securing the diopter ring. The defect may cause loss of adjustment function, blurred vision, and in rare cases, urinary tract perforation.
Volcano Corp is recalling 11 Philips OmniWire Pressure guide wires distributed in Washington, Wisconsin, and Canada due to a potential failed sterilization process.
Washington Homeopathic Products recalled Bacillinum Pulmo homeopathic drug due to manufacturing practice deviations. The Class II recall, initiated in May 2022 and terminated in May 2023, affected nationwide distribution.
Afaxys Pharma is recalling 79,339 prefilled syringes of medroxyprogesterone acetate because the manufacturer could not assure sterility. The syringes were distributed nationwide.
Hand Sanitizer LLC is recalling Say Goodbye to Germs hand sanitizer bottles due to CGMP deviations. FDA testing found acetaldehyde and acetal levels above acceptable limits.
A.P. Nonweiler is recalling its 80% alcohol antiseptic hand sanitizer because FDA testing found acetaldehyde and acetal above safe specification limits. The product was distributed in Wisconsin and Virginia.
Medtronic recalls 3,944 Crome and Cobalt ICDs and CRT-Ds due to a potential telemetry error affecting device communication with external monitors.
Washington Homeopathic Products is recalling Pyrogenium homeopathic remedies in multiple potencies due to current Good Manufacturing Practice (cGMP) deviations. The firm initiated this voluntary recall affecting 6,782 bottles distributed nationwide.
Walmart is recalling all lots of Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets nationwide. The product was marketed without FDA approval based on unapproved labeling claims.
Walmart Inc is recalling Artri King Reforzado con Ortiga Omega 3 Tablets nationwide because the product was marketed as a drug without FDA approval. All lots are affected.
Washington Homeopathic Products is recalling Candida Parapsilosis homeopathic remedies distributed nationwide due to manufacturing practice deviations. The recall affects 134 bottles under lot numbers 22315 and 26502.
Washington Homeopathic Products is recalling Candida Albicans homeopathic remedy due to manufacturing quality control violations. The voluntary recall affects 1,047 bottles distributed nationwide.
Washington Homeopathic Products is recalling Pertussinum in multiple potencies nationwide due to manufacturing practice deviations. Affected lot numbers are 18829, 20142, and 25410.
Washington Homeopathic Products is recalling Diphtherinum homeopathic remedy (potencies 14C, 30C, 200C) distributed nationwide due to manufacturing practice deviations (cGMP violations). Affected lots: 20332, 20333.
Washington Homeopathic Products is voluntarily recalling Streptococcinum homeopathic drug in multiple potencies due to manufacturing practice deviations. No illnesses have been reported.
Washington Homeopathic Products is recalling Influenzinum in multiple potencies due to manufacturing process deviations. The recall affects approximately 6,400 units distributed nationwide.
AMS Packaging is recalling Premium Nature Instant Hand Sanitizer nationwide because FDA analysis found some bottles contain less ethanol than labeled.
Washington Homeopathic Products recalled Medorrhinum liquid pellets nationwide due to deviations from manufacturing standards. The product was distributed in 49 glass amber bottles.
Washington Homeopathic Products is recalling Morbillinum in multiple potencies due to manufacturing practice deviations. No illnesses have been reported.
Washington Homeopathic Products is recalling Syphilinum homeopathic products in multiple potencies due to current good manufacturing practice deviations. The affected products were distributed nationwide.
Washington Homeopathic Products is recalling Tuberculinum homeopathic drug in multiple potencies due to manufacturing practice deviations. The voluntary recall affects product distributed nationwide.
Washington Homeopathic Products is recalling Vaccinotoxinum homeopathic remedies (lot numbers 2512K and 20280) distributed nationwide due to cGMP manufacturing deviations. The voluntary recall was initiated by the firm in May 2022.
Washington Homeopathic Products is recalling Anthracinum liquid pellets due to manufacturing process deviations. The voluntary recall affects 219 bottles distributed nationwide.
Washington Homeopathic Products recalls Colibacillinum homeopathic drug products due to manufacturing practice deviations. The recall involves 206 bottles distributed nationwide; the manufacturer voluntarily initiated it in May 2022.
Washington Homeopathic Products is recalling Tuberculinum Bovinum homeopathic remedy due to current good manufacturing practice deviations. No illnesses have been reported.
Proterra is recalling 185 High Voltage Junction Box DC Links because a battery cable may not be properly connected, risking power loss, ground short circuits, or fire.
Fabform is recalling 2018-2022 FLR-D, FLRR-D, and DBX trailers because a rubber stop may break, allowing the utility gate to detach and increase crash risk.
Daimler Trucks North America is recalling 258 Thomas Built Buses and FCCC Saf-T-Liner models due to a software defect that may cause unexpected engine shutdowns, increasing crash risk.
Daimler Trucks recalls certain Thomas Built school buses (2020-2023) due to an engine control module defect that can cause unexpected engine shutdown while driving, increasing crash risk.
BorgWarner is recalling specific EGR valves where a loose washer may cause the valve to stick open, resulting in an unexpected loss of drive power.
Heartland is recalling 2022 travel trailers because quick disconnect fittings in the LP gas system may crack, causing a gas leak that could lead to a fire. Dealers will replace the fittings free of charge.
Nova Bus is recalling one specific Sheppard model steering gear that may have been assembled incorrectly. The defect can cause the gear to fracture, leading to loss of steering control.
Triple E is recalling 2021-2022 Unity and Wonder RVs because damaged burner control valves may cause a gas leak, increasing fire risk.
Gillig is recalling 2019-2022 Low Floor electric buses because a cable connector may lose electrical connectivity, causing the vehicle to unexpectedly switch to Neutral.
Cruiser RV is recalling 2022 travel trailers with potentially cracked LP gas system fittings that may leak, creating a fire hazard. Dealers will inspect and replace affected fittings free of charge.
Autocar is recalling 2019-2022 Xpeditor trucks due to water intrusion in the external fuse box, which may short circuit and cause unexpected vehicle stalls, increasing crash risk.
Isuzu is recalling certain 2022 N-Series trucks with 6.0L engines for incorrectly wired oil pressure sensor assemblies. The defect prevents driver alerts to low oil pressure, risking engine stall and crashes.
Navistar is recalling certain 2022-2023 IC CE School Buses because their steering gears may have been assembled incorrectly and could fracture, causing a loss of steering control and increasing crash risk.
Sienhua Group is recalling about 580,000 WarmWave and Hunter Oscillating Ceramic Tower Heaters because the cord and plug can overheat during use, posing fire and burn risks. The company has received eight reports of fires at the plug or cord and dozens of reports of overheating.
Irbit Motorworks is recalling 2012-2017 Ural motorcycles because improperly tightened wheel spokes may damage rims or cause wheel lock-up, increasing crash risk.
Honda is recalling 2006-2014 Ridgeline vehicles sold or registered in 23 states and D.C. because road salt corrosion may cause the fuel tank to detach and leak.
TJX is recalling approximately 30,600 Nest Swing Egg Chairs sold at Marshalls, T.J. Maxx, HomeGoods, and Homesense stores because the chairs can tip over or collapse when occupied, posing a fall hazard.
Navistar is recalling 2022-2023 International commercial vehicles with defective steering gears that may fracture and cause loss of steering control. Contact your dealer or Navistar at 1-800-448-7825 for inspection and free replacement.
Kroger-brand acetaminophen tablets in 225-count bottles lack required child-resistant packaging, posing a poisoning risk to young children if ingested. About 25,660 units were sold nationwide from December 2021 through March 2022.
Time-Cap Labs is recalling Kroger-brand aspirin and ibuprofen products because the bottles lack child-resistant packaging required by law, posing a poisoning risk to young children who may swallow the contents.
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