Safety Recalls
RSS ↗17,560 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 5,651–5,700 of 17,560
- Class II
Food Recall · October 3, 2025
Frozen Coconut bar Net wt. 4oz (113g) single bars packed in a plastic cup. UPC: 61058590845. Crafted by Fruitique International Miami USA 33016. Phone 1(888)960-6024Undeclared sulfites in product label.
- Class II
Food Recall · October 3, 2025
Italian style shredded cheese blend (containing low-moisture part-skim mozzarella, provolone, parmesan, romano, fontina and asiago cheese), individually packaged in a plastic bag, as: 1) Brookshire'sPotential metal fragments from supplier raw material (downstream recall)
- Class II
Medical Device Recall · October 3, 2025
Integra LifeSciences Corp. (NeuroSciences)
TruDi¿ Navigation System - Multi Instrument Adapter; - Manufacturer's Product Number (Catalog Number): EM-2025-000F Rev 00 or Rev 01;It was determined that when the navigation system is configured with specific revision combinations of the Multi Instrument Adapter together with the Patient Tracker the system may not meet its specified accuracy for visual verification of device location within the patient s anatomy.
- Class II
Medical Device Recall · October 3, 2025
MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.
- Class II
Food Recall · October 3, 2025
Good & Gather Mozzarella & Parmesan shredded cheese blend, Fine Cut, 8 oz., individually packaged in a plastic bag, UPC 8523903856, 12/casePotential metal fragments from supplier raw material (downstream recall)
- Class II
Drug Recall · October 3, 2025
Advanced Pharmaceutical Technology, Inc.
TESTO-100 CIII (testosterone 100 mg), 10 Sterile Pellets per carton, Rx only, Manufactured by: Advanced Pharmaceutical Technology, 132 South Central Avenue, Elmsford, NY 10523, NDC# 57377-100-01Lack of Assurance of Sterility: Potential microbial contamination of subcutaneous pellets.
- Class II
Medical Device Recall · October 3, 2025
MC3 VitalFlow Console, REF 58100; Blood pump of ecmoAs of August 6, 2025, Medtronic has received eleven reports of VitalFlow Consoles displaying an E70 error code during normal operation. When this occurs, the touch screen may become temporarily unresponsive and go blank for up to two minutes before recovering to full functionality. Importantly, the console continues to maintain set pump speed and function throughout.
- Class II
Food Recall · October 3, 2025
Low-moisture part-skim mozzarella shredded cheese, individually packaged in a plastic bag, as: 1) Always Save - Shredded, 5 lb., UPC 7003865782, 4/case 2) Borden - Shredded, 8 oz., UPC 5300007162, 6Potential metal fragments from supplier raw material (downstream recall)
- Class II
Food Recall · October 3, 2025
Mozzarella and provolone shredded cheese blend (containing low-moisture part-skim mozzarella and not-smoked provolone cheeses), individually packaged in a plastic bag, as: 1) Freedom's Choice Pizza BPotential metal fragments from supplier raw material (downstream recall)
- Class II
Food Recall · October 3, 2025
COCACOLA SOUTHWEST BEVERAGES LLC
Sprite 12oz Can 35 pack 49000058482 / JUN2926MAA Sprite 12oz Can 12 pack 49000028928 / JUN2926MAA Sprite 12oz Can 12 pack 49000028928 / JUN3026MABPotential presence of foreign material (metal) in the product
- Class II
Food Recall · October 3, 2025
COCACOLA SOUTHWEST BEVERAGES LLC
Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12oz Can - 35 pack 49000058468 / JUN2926MAAPotential presence of foreign material (metal) in the product
- Class I
Medical Device Recall · October 2, 2025
IV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave, Shut Off) w/Clave, Luer Lock, REF: B33359; 23" (58 cm) 150 ml Burette Set (w/Shut Off), MicroClave, Clamp, REF: B9213; 70" (178 cm)IV Gravity burette administration set burette component is missing an internal shutoff valve intended to stop fluid flow, which if used may result in delay in therapy during setup, over delivery/unrestricted flow, or air may be infused into the body.
- Class I
Food Recall · October 2, 2025
Smoked Mozzarella Penne Salad-Small, Clam shell and Bowl, 4 lbs 8 oz, Individual Unit, Keep Refrigerated, UPC 246511000000Recall notification from supplier of Potential listeria contamination.
- Class II
Food Recall · October 2, 2025
Gluten Free Bean & Rice Burrito. 12 retail units per case. 5.5oz/retail unit. UPC code 042272003525. Frozen.Potential contamination with foreign objects.
- Class I
Medical Device Recall · October 2, 2025
CEREPAK Detachable Coil System - Name/REF: UNIFORM 2MM X 2.5 CM/FCX100202, UNIFORM 2.5MM X 3.3 CM/FCX100253, UNIFORM 3MM X 5.4 CM/FCX100305, UNIFORM 3.5MM X 6.6 CM/FCX100356, UNIFORM 4MM X 7.5 CM/FCX1Detachable coils system may fail to detach, which could result in hemorrhagic and ischemic stroke, procedural delays, or the need for additional surgical intervention.
- Unclassified
Consumer Product Recall · October 2, 2025
Ningbo Leha E-Commerce Co., Ltd., of China doing business as Amazon seller Almpal
Dissolved Oxygen Test KitsThe recalled test kits contain a bottle of sulfuric acid, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The test kits violate the mandatory standard for child-resistant packaging because the bottle of sulfuric acid is not child-resistant, posing a risk of serious injury or death from poisoning, if the contents are swallowed by young children.
- Class I
Food Recall · October 2, 2025
Smoked Mozzarella Penne Salad, bulk, UPC 256616000000Recall notification from supplier of Potential listeria contamination.
- Class II
Medical Device Recall · October 2, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;The motorized longitudinal movement of the FlexArm stand may be inconsistent (not smooth) and eventually may become unavailable. This issue is due to grease leakage from the bearings and/or anti-corrosion oil applied on the bearings, because of which the lubrication on the ceiling rail may be excessive, reducing the friction between the rails and the friction wheel. Expansion to add additional model.
- Unclassified
Consumer Product Recall · October 2, 2025
Blossom Blanks, LLC dba Blossom, of Gadsden, Alabama
Blossom Children's Loungewear setsThe recalled children's loungewear sets violate the mandatory flammability standard for children's sleepwear, posing a risk of burn injuries or death to children.
- Unclassified
Consumer Product Recall · October 2, 2025
Changzhou Hengze Home Furnishing Co., Ltd, of China
Gunaito 10-Drawer DressersThe recalled dressers are unstable, if they are not anchored to the wall, posing serious tip-over and entrapment hazards, that can result in injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.
- Unclassified
Consumer Product Recall · October 2, 2025
BP125, BatPak 2F and BatPak 3F Power BanksThe recalled power banks' lithium-ion batteries can overheat and ignite, even when not in use, posing fire and burn hazards.
- Class I
Food Recall · October 2, 2025
Smoked Mozzarella Penne Salad-Large, Clam shell and Bowl, 9 lbs, Individual Unit, Keep Refrigerated, UPC 246512000000Recall notification from supplier of Potential listeria contamination.
- Unclassified
Vehicle Recall · October 2, 2025
2024 HYUNDAI SANTA FE, 2025 HYUNDAI SANTA FEAn electrical short increases the risk of a fire.
- Unclassified
Consumer Product Recall · October 2, 2025
In Motion Design Inc., of Paramount, California
Evermore Surprise EggsThe toy airplane inside the egg contains levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.
- Class II
Food Recall · October 2, 2025
LMPS 1.5" BULK MOZZARELLA. 11" X 14" X 1.5 slabs, approximately 10 lbs. each. Approx. 1125 lbs. packaged in corrugated totes. Product Code 100003207. Refrigeration at 34-40F.Possible stainless steel pieces in product.
- Class II
Medical Device Recall · October 1, 2025
Magseed Pro 7 cm soft tissue marker. Model Number: MS2-17-1-07. Product Description: The Endomag Magseed Pro Magnetic Marker System is a sterile, single use device composed of a marker preloaded inPotential for contamination with cotton fibers.
- Class II
Medical Device Recall · October 1, 2025
Medline RenewalLigasure Blunt Tip Sealer/Divider, NanoCoated Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic &Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
- Class II
Medical Device Recall · October 1, 2025
Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated, Compatible with FT10 Generator 44 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, LaparoscopiMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
- Class I
Food Recall · October 1, 2025
Scott & Jon s Shrimp Scampi with Linguine, 9.6 oz.Contains Linguine manufactured by Nate's Fine Foods LLC recalled for Listeria monocytogenes and implicated in ongoing outbreak
- Class II
Medical Device Recall · October 1, 2025
Medline Renewal LigaSure Exact, Dissector without Nano-Coating 21cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical Cutting And Coagulation DeviceMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
- Class II
Medical Device Recall · October 1, 2025
Medline Renewal LigaSure Small Jaw Instrument (Purple/White), Compatible with FT10 Generator 18.8 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, LaparoscopiMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
- Class I
Food Recall · October 1, 2025
White Chocolate Coconut Bundt Cake - Net Weight 3 lbs 12 oz Contains: Wheat, Soy, Milk, Eggs No UPCUndeclared allergen ingredient (Wheat) in Ready-to-eat frozen cakes.
- Class I
Medical Device Recall · October 1, 2025
Automated Impella Controller (AIC), used for left heart support blood pump, labeled as the following with corresponding Product Codes: 1. Impella Controller, Packaged, AU; Product Code: 0042-0000-AU.Potential cybersecurity vulnerabilities related to the operating system in the Automated Impella Controller (AIC).
- Class II
Medical Device Recall · October 1, 2025
Beckman Coulter UniCel DxI 800, Part Numbers: 973100, A71456; Photometric Chemistry AnalyzerAn internal investigation has determined that due to defective sub-components within the gantry assembly, a z-axis CAD movement motion error may occur and cause an analyzer to enter a Not Ready or Paused state, leading to a delay in obtaining results.
- Class II
Medical Device Recall · October 1, 2025
Beckman Coulter UniCel DxI 600, Part Numbers: A71460, A30260; Photometric Chemistry AnalyzerAn internal investigation has determined that due to defective sub-components within the gantry assembly, a z-axis CAD movement motion error may occur and cause an analyzer to enter a Not Ready or Paused state, leading to a delay in obtaining results.
- Class I
Medical Device Recall · October 1, 2025
Siemens Medical Solutions USA, Inc
MAGNETOM Cima.X Upgrade. Model Number: 11689304.There is a potential for an ice blockage to form or currently exist within the primary and/or the auxiliary venting paths of the magnet helium containment venting system. In the event of a quench when both venting paths are blocked, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
- Class II
Medical Device Recall · October 1, 2025
Medline Renewal LigaSure Maryland Jaw Sealer/Divider NanoCoated, Compatible w/FT10 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & EndoscopiMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
- Class II
Medical Device Recall · October 1, 2025
Medline Renewal LigaSure Impact Curved Large Jaw Sealer/Divider, Compatible with FT10 Generator, FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & EMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
- Class II
Medical Device Recall · October 1, 2025
Philips Medical Systems DMC GmbH
DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.
- Class II
Medical Device Recall · October 1, 2025
Philips Medical Systems DMC GmbH
DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.
- Class II
Medical Device Recall · October 1, 2025
Medline Renewal LigaSure Maryland Jaw Sealer/Divider Nano Coated, Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, LaparoscopMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
- Class II
Medical Device Recall · October 1, 2025
Thermo scientific MAS Omni CARDIO, Liquid Assayed Integrated Cardiac Control, Model/Catalog Number: OCRD-L, OCRD-101, OCRD-202, OCRD-303, OCRD-SP, OCRD-MP, OCRD-UL; Product Description: In Vitro DiagnThe firm received complaints from customers reporting vial-to-vial variability when using the control with high sensitivity Troponin I assays. This defect may lead to as delay in patient results for hs Troponin I assays.
- Class II
Medical Device Recall · October 1, 2025
Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated, Compatible with FT10 Generator 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic &Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
- Class II
Medical Device Recall · October 1, 2025
Medline Renewal Ligasure Impact Sealer/Divider NanoCoated, Compatible with FT10 Generator 18cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & EndMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
- Class II
Medical Device Recall · October 1, 2025
Philips Medical Systems DMC GmbH
Radiography 7300 C; Model Number: 712037;Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.
- Class II
Medical Device Recall · October 1, 2025
Philips Medical Systems DMC GmbH
CombiDiagnost R90; Model Number: 709031;Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.
- Class I
Food Recall · October 1, 2025
Carrot Bundt Cake - Net Weight 4 lbs Contains: Wheat, Soy, Milk, Eggs, Tree Nuts No UPCUndeclared allergen ingredient (Wheat) in Ready-to-eat frozen cakes.
- Class II
Medical Device Recall · October 1, 2025
Philips Medical Systems DMC GmbH
ProxiDiagnost N90; Model Number: 706110;Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.
- Class II
Medical Device Recall · October 1, 2025
Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated, Compatible with FT10 Generator 44cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic &Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
- Class II
Medical Device Recall · October 1, 2025
Brand Name: ReQuest Measles IgG Product Name: Rubeola IgG Enzyme Linked Immunoabsorbant Assay Model/Catalog Number: 01-190 Software Version: N/A Product Description: Measles IgG tests, performed uDue to distributing the measles IgG IVD without a premarket approved/cleared.