Archive
526 recalls were announced in June 2024.
Of the 526 recalls this month scored against our rubric, 3% are Critical, 25% are Severe.
Which agencies issued them
Certain 2023 Jeep Grand Cherokee vehicles have a loose second-row seat belt buckle bolt that may not properly restrain occupants during a crash. Dealers will inspect and tighten the bolt free of charge.
Black Diamond Equipment is recalling Neve Strap Crampons and Accessory Kits because screws connecting the heel cup to the crampon can loosen, causing the heel cup to detach and creating a fall hazard. The firm has received three reports of incidents but no injuries have been reported.
Altec is recalling 2023-2024 aerial devices and related truck-mounted equipment due to lighting wire harness overload that may prevent vehicle lights from illuminating, reducing visibility to other drivers and increasing the risk of crashes.
Airstream is recalling 2024 Interstate motorhomes because a missing 12-volt fuse could allow the supply wire to overheat, increasing the risk of fire.
Danisco USA Inc. is recalling Grindsted Hi-Dress CDS 1880 Stabilizer and Emulsifier System due to potential Salmonella contamination. The product was distributed to facilities across multiple US states, Canada, and Mexico.
Megadyne Medical Products is recalling its MEGA SOFT Pediatric Patient Return Electrode due to reports of patient burns during electrosurgical use. Approximately 1,270 units distributed worldwide are affected.
Danisco USA Inc. is recalling GS 1134 Kreme WIP, a food ingredient product, due to potential Salmonella contamination affecting multiple U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Creamer 2395 Stabilizer and Emulsifier System due to potential Salmonella contamination. The product was distributed across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Germantown Gard (A) Preservative due to potential Salmonella contamination. The recall affects 21,000 kg distributed across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Yogurt 7133 Stabilizer System due to potential Salmonella contamination. The affected ingredient was distributed to multiple U.S. states, Canada, and Mexico.
Danisco USA Inc. has issued a recall of Grindsted ASC 2354 Stabilizer and Emulsifier System for potential Salmonella contamination. The product is distributed to multiple US states, Canada, and Mexico.
Danisco USA Inc. recalls Grindsted Turkey Hill 1512 NF NSA Stabilizer and Emulsifier System (10 lot numbers) due to potential Salmonella contamination. The 2,270-pound product was distributed to 28 US states, Canada, and Mexico.
Danisco USA Inc. recalls ASC 2138 Stabilizer and Emulsifier System due to potential Salmonella contamination. Affected product distributed across US, Canada, and Mexico.
The FDA recalled 3,138 Arrow Ultra 8 intra-aortic balloon catheter kits globally due to potential balloon inflation failure and helium pathway damage that could compromise critical cardiac support.
Danisco USA Inc. is recalling Grindsted Creamer 2160 System bags due to potential Salmonella contamination. The recall affects 31,865.40 kg distributed across the US, Canada, and Mexico.
Hormel Foods is recalling PLANTERS Honey Roasted Peanuts 4oz packages due to possible Listeria monocytogenes contamination. Approximately 15,132 packages were distributed to retailers in FL, GA, AL, NC, and SC.
Multiple brands of yogurt pretzels are being recalled due to potential Salmonella contamination. Affected products were distributed in California and Washington.
Danisco USA Inc. recalls Grindsted Sour Cream 6563 stabilizer system for potential Salmonella contamination affecting 33,600 kg distributed across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Germantown Stabilizer 1772-II, a food stabilizer and emulsifier system, due to potential Salmonella contamination. The product was distributed across the U.S., Canada, and Mexico.
Danisco USA Inc. is recalling CRE-90 (RO1) Stabilizer System due to potential Salmonella contamination. The product was distributed across multiple US states, Canada, and Mexico.
Bonneval Foods is recalling 45 pounds of BBQ Pork Skins because the product contains undeclared wheat and soy allergens. The product was sold in Louisiana and Mississippi.
Forest River is recalling 3,192 school buses because the restraining barrier may not provide sufficient protection in a crash, increasing injury risk.
Danisco USA Inc. is recalling Avicel-plus GP 1615 Stabilizer System FCC due to potential Salmonella contamination. The affected bulk food additive was distributed to manufacturers across multiple U.S. states, Canada, and Mexico.
Endera is recalling 2021-2024 school buses because seat assemblies may lack reinforcing washers, causing non-compliance with safety standards and increasing injury risk.
Danisco USA Inc. is recalling Reese SG FR Sweetener Blend, CM50 due to potential Salmonella contamination. The recall affects product distributed across 24 US states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Iced Coffee 6752 Stabilizer System in 50 lb bags due to potential Salmonella contamination. The recall affects product distributed across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted CFF 1455 Stabilizer System due to potential Salmonella contamination. The product was distributed to commercial customers in 24 US states, Canada, and Mexico.
Danisco USA Inc. is recalling GSD 0911 Stabilizer due to potential Salmonella contamination. The food ingredient additive was distributed to manufacturers across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted SSD 6018 Stabilizer System due to potential Salmonella contamination. The product has been distributed to customers in the United States, Canada, and Mexico.
Arrow International is recalling intra-aortic balloon catheter kits due to potential inflation failure, catheter damage, and helium loss that could cause serious health consequences.
Arrow International is recalling its UltraFlex Intra-Aortic Balloon Catheter Kit because of infrequent device malfunction that could lead to serious health consequences. 44,807 units are affected worldwide.
Hormel Foods is recalling Planters Deluxe Lightly Salted Mixed Nuts (8.75 oz) due to possible Listeria monocytogenes contamination. The recall affects 6,804 cans distributed to five southeastern states.
Danisco USA Inc. is recalling Yogurt 6626 Stabilizer System due to potential Salmonella contamination. The product was distributed across 23 US states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Whipped Cream #2 stabilizer system due to potential Salmonella contamination. The product was distributed in 24 US states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Creamer 2103 Stabilizer and Emulsifier System due to potential Salmonella contamination. Approximately 36,265 kg was distributed across multiple U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted SSD 5731 Non-GMO Stabilizer System due to potential Salmonella contamination. The product was distributed across multiple U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted GSD 1076 Stabilizer and Emulsifier System in 50-pound bags due to potential Salmonella contamination. The product was distributed to multiple US states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted IcePro 2427 TH Stabilizer System due to potential Salmonella contamination. The product was distributed across the United States, Canada, and Mexico.
County Road Seafood is recalling Crab Cake 2 Pack products distributed to NC and SC because they contain undeclared egg. Consumers with egg allergies should not consume this product.
Danisco USA Inc. is recalling Grindsted Sweet Roll Dough Blend 2 Stabilizer & Emulsifier System due to potential Salmonella contamination. The product was distributed across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Sweetlife CINN. Roll BAS Stabilizer & Emulsifier System due to potential Salmonella contamination. The product was distributed across 28 U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Creamer 1817 Stabilizer System due to potential Salmonella contamination. The product was distributed to 23 U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Germantown Dari Whip II, a food stabilizer and emulsifier product, due to potential Salmonella contamination. The product was distributed across 23 US states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Iced Coffee 6880 Stabilizer System because of potential Salmonella contamination. The affected product (lot 1204625920) was distributed in the US, Canada, and Mexico.
Danisco USA Inc. is recalling Germantown Gard Preservative (25 kg bags) due to potential Salmonella contamination. The product was distributed across the US, Canada, and Mexico.
Danisco USA Inc. has recalled Grindsted SSD 6242 Stabilizer System due to potential Salmonella contamination. The recall affects 884.52 kg of product distributed to the United States, Canada, and Mexico.
Danisco USA Inc. is recalling Germantown Enhance Plus Stabilizer System (lot 1204572178) due to potential Salmonella contamination. The product was distributed across multiple US states, Canada, and Mexico.
Danisco USA Inc. is recalling Cremodan SL-64-A Stabilizer System due to potential Salmonella contamination. The product was distributed across multiple U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted WCS 1265 Stabilizer and Emulsifier System due to potential Salmonella contamination. The product was distributed across the US, Canada, and Mexico.
Getinge's sevoflurane vaporizer component may degrade into hydrogen fluoride, posing inhalation and skin exposure risks to healthcare workers and patients. The FDA Class I recall affects 120 units distributed across six U.S. states.
Danisco USA Inc. is recalling Grindsted TH GSD 2272 Stabilizer and Emulsifier System distributed in bulk due to potential Salmonella contamination. The product was distributed across the U.S., Canada, and Mexico.
Danisco USA Inc. recalls CRE-90 (RO1) 25 KG bags due to potential Salmonella contamination. The product was distributed across 24 U.S. states, Canada, and Mexico.
PACCAR is recalling 2025 Kenworth and Peterbilt trucks due to improperly heat-treated ball studs in steering assemblies that may break, causing loss of steering control.
A defective drip chamber in the Alaris Pump Infusion Set may detach from the tubing, potentially delaying treatment or causing unintended exposure to medications. BD is recalling approximately 11,300 units distributed across the US and Canada.
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reports of the slider GDS swivel rod separating from the swivel core. Approximately 53,308 units are affected worldwide.
Schreiber Foods Inc is recalling whipped cream cheese spread sold under multiple store brands due to potential Salmonella contamination. Consumers should return the product to the retailer.
Nihon Kohden's BSM-3000 Series Bedside Monitors may produce false SpO2 probe failure alarms due to a software issue. Healthcare facilities should contact the manufacturer for guidance.
Atrium Medical is recalling ADVANTA VXT vascular grafts following complaints of separation between the slider component and swivel core.
Schreiber Foods Inc is recalling 835,721 units of Essential Everyday Blueberry Cream Cheese Spread (8 oz) due to potential Salmonella contamination. No illnesses have been reported.
Schreiber Foods Inc is recalling Strawberry Cream Cheese Spread sold under brands including Fareway, Happy Farms, Hy-Vee, and Schnuck due to potential Salmonella contamination. Approximately 835,721 units were distributed across multiple states and Puerto Rico.
Schreiber Foods is recalling Chive and Onion Cream Cheese Spread sold under the Fareway, Happy Farms, and Hy-Vee brands due to potential Salmonella contamination. Affected consumers should not consume the product.
Schreiber Foods is recalling Ranch Garlic Cream Cheese Spread due to potential Salmonella contamination. Approximately 835,721 units were distributed to 19 states and Puerto Rico.
Schreiber Foods is recalling cream cheese spread sold under Dunkin, Happy Farms, Hy-Vee, Piggly Wiggly, and Schnucks brands due to potential Salmonella contamination. The recalled products were distributed to multiple states and Puerto Rico.
Atrium Medical Corporation recalls Advanta VXT vascular grafts due to separation of internal swivel components. Approximately 53,308 units worldwide are affected, with the slider GDS swivel rod potentially separating from its core.
Atrium Medical recalls ADVANTA VXT vascular grafts due to reported separation of the slider swivel rod from its core, creating a gap between components. No injuries reported.
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. No injuries have been reported.
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. Approximately 53,308 units have been affected worldwide.
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reports of the slider rod separating from the swivel core, which could impair proper device function.
Atrium Medical Corporation is recalling its ADVANTA VXT vascular grafts due to complaints of swivel rod separation from the swivel core, which could affect device function and patient safety.
Atrium Medical recalls ADVANTA VXT vascular grafts due to reports of the Slider GDS Swivel Rod separating from the Swivel Core. The internal component separation could compromise device function.
The ADVANTA VXT vascular graft is being recalled because its slider rod can separate from the swivel core, creating a gap between components. No injuries have been reported.
Atrium Medical is recalling 53,308 ADVANTA VXT vascular grafts worldwide due to reported separation of the slider rod from the swivel core, with a gap observed between the components.
Atrium Medical is recalling 53,308 ADVANTA VXT vascular grafts due to reports of Slider GDS Swivel Rod separation from the Swivel Core. Component separation could compromise device function.
Atrium Medical's ADVANTA VXT vascular graft may experience separation of the slider mechanism from its core, affecting over 11,000 US units. No injuries have been reported.
Newport has recalled Class II laser systems because their key-actuated safety switch can be removed while the laser remains on, violating federal safety requirements.
Atrium Medical recalls FLIXENE vascular grafts due to reported separation between the slider rod and swivel core. Affected grafts may fail to function properly if deployed.
Atrium Medical recalls ADVANTA VXT vascular grafts due to separation of the slider swivel rod from its core. The defect affects 53,308 units distributed worldwide.
Atrium Medical recalls FLIXENE vascular grafts due to reported separation of the Swivel Rod from the Swivel Core, creating gaps that could affect device function. Over 53,000 units worldwide are affected.
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to separation of the Slider GDS Swivel Rod from the Swivel Core. Over 53,000 units affected worldwide.
Atrium Medical Corporation is recalling the Advanta VXT vascular graft due to reports of the swivel rod separating from the swivel core. The recall affects approximately 53,308 units distributed in the United States and worldwide.
CORENTEC is recalling LOSPA Tibial Insert knee implant components due to an unsupported 10-year expiration date. Patients with these devices should consult their physician.
Panera Kitchen Sink Cookie dough pucks from Rise Baking Company are being recalled due to potential Salmonella contamination. The recall covers 29,019 cases distributed across 20 U.S. states.
The Arial mobile application experiences frequent restarts on iOS 17.4 and 17.5, causing alert overload, communication failures, and offline status in healthcare facilities.
WAVi Co. is recalling 281 units of the WAVi Research EEG Desktop System following an FDA-issued Warning Letter. The company requested the return of components due to closure of their research study.
Della Fattoria, LLC is recalling 115 loaves of Della Fattoria Seeded Wheat Bread sold in California because the product contains sesame seeds but sesame is not declared on the label.
CORENTEC's LOSPA Patella Component knee implants are recalled due to an unsupported 10-year expiration date. Thirty-five units were distributed nationwide.
Medline is recalling 25.2 million Luer Lock disposable syringes because testing documentation does not confirm they deliver accurate volumes across their claimed capacity. The inaccuracy may pose a risk to patient health.
Verathon is recalling GlideScope Core 15-inch monitors due to software issues causing potential image loss or degradation. Approximately 2,568 units were distributed across the US and internationally.
Glenmark Pharmaceuticals is recalling Rizatriptan Benzoate 10mg tablets nationwide due to N-nitroso impurity levels exceeding FDA acceptable limits, affecting 13,296 cartons.
Becton Dickinson is recalling 2,061 kits of BD SARS-CoV-2 Reagents for BD MAX Systems because they may produce false negative results due to decreased enzyme activity. The kits were distributed nationwide and internationally.
Della Fattoria, LLC is recalling Della Fattoria Sicilian Semolina bread due to missing sesame seed declarations on the label. Consumers with sesame allergies should not consume this product.
Schreiber Foods is recalling Garden Vegetable Cream Cheese Spread sold under multiple brands due to potential Salmonella contamination. Approximately 835,721 units were distributed to 19 states and Puerto Rico.
Philips HA FlexTrak II patient transport trolleys may leak hydraulic oil onto the floor when pressed, creating a slip and fall hazard. About 590 units are affected worldwide.
Simultaneous ECG measurements with multiple devices can cause electrical interference that may prevent this defibrillator from functioning properly. The recall affects 1,745 units distributed nationwide.
Oil may leak from the HA FlexTrak patient transport device when the hydraulic pedal is pressed, creating a potential slipping or falling hazard on the floor.
Glenmark Pharmaceuticals recalls certain Rizatriptan Benzoate tablets due to N-Nitroso Desmethyl Rizatriptan impurity levels exceeding FDA acceptable limits. The affected lots were distributed nationwide.
Stryker Neurovascular recalls certain lots of Synchro SELECT Guidewires due to PTFE coating damage that may occur when using a backloading technique. The damage is caused by sharper-than-intended edges on older introducer versions.
Medline Industries is recalling over 5 million Luer Slip disposable syringes because testing documentation does not confirm they deliver accurate volumes across their claimed capacity range. This poses a risk to patient health.
Philips is recalling the HA FlexTrak patient transport trolley due to potential oil leaks from the hydraulic system that create slipping and falling hazards. Approximately 100 units have been distributed worldwide.
Medline is recalling 67,811 units of sterile iris scissors because the tip protector may detach during use. The recall affects units distributed nationwide and internationally.
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