Safety Recalls
RSS ↗15,259 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 5,051–5,100 of 15,259
- Class II
Medical Device Recall · August 13, 2025
UniCel DxH 900 COULTER Cellular Analysis System, configured with the Led HGB Photometer REF: C11478Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.
- Class I
Food Recall · August 13, 2025
Tuscan Artichoke and Mozzarella Salad; Keep Refrigerated, NET WT: 8.5 OZ, UPC# 6 82906 90935 1 Manufactured by Fresh and Ready Foods LLC, San Fernando, CA 91340undeclared allergen (Wheat and Milk) on ready to eat sandwiches.
- Class III
Medical Device Recall · August 13, 2025
Penner Pacific Bathing Spa, Model Numbers 360020-1PThe device does not bear a unique device identifier.
- Class II
Medical Device Recall · August 13, 2025
Philips CT systems labeled as the following: 1. Ingenuity Core128 / Elite China, Model Number: 728324.The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- Class I
Food Recall · August 13, 2025
Spanish Club Ciabatta; Keep Refrigerated, NET WT: 10.5 OZ, UPC# 6 82906 90933 7 Manufactured by Fresh and Ready Foods LLC, San Fernando, CA 91340undeclared allergen (Wheat and Milk) on ready to eat sandwiches.
- Class III
Medical Device Recall · August 13, 2025
Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, 360030-1C, 360030-XC, 360030-XCT, 360030-1CTS, 360030-XCTS, 3600301-CTS, 360030-XCE, 36The device does not bear a unique device identifier.
- Class II
Medical Device Recall · August 13, 2025
Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306.The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- Class II
Medical Device Recall · August 13, 2025
Philips CT systems labeled as the following: 1. IQon Spectral CT, Model Number: 728332.The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- Class II
Medical Device Recall · August 13, 2025
Philips CT systems labeled as the following: 1. CT 6000, Model Number: 728307.The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- Class III
Medical Device Recall · August 13, 2025
Penner Pacific Bathing Spa, Model Numbers 760010-1, 770010-1The device does not bear a unique device identifier.
- Class II
Medical Device Recall · August 13, 2025
Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel, Model Number: 728235. 2. Brilliance CT 64 Channel, Model Number: 728231. 3. Ingenuity Flex, Model Number: 728317The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
- Class III
Medical Device Recall · August 13, 2025
Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A, 361910-XThe device does not bear a unique device identifier.
- Class III
Medical Device Recall · August 13, 2025
Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XLThe device does not bear a unique device identifier.
- Class III
Medical Device Recall · August 13, 2025
Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-XThe device does not bear a unique device identifier.
- Class I
Food Recall · August 12, 2025
Wegmans Assorted Cheese Flight - Varies (sold by the lb) - Black Plastic container with clear lid UPC: 2-77100-XXXXX-5 (X - varies by weighted price)Products may be contaminated with Listeria monocytogenes
- Class I
Medical Device Recall · August 12, 2025
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCMC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.
- Class I
Medical Device Recall · August 12, 2025
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.
- Class I
Medical Device Recall · August 12, 2025
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.
- Class II
Food Recall · August 12, 2025
PURE CANE GRANULATED SUGAR, NET WT 50 LB (22.67kg), Distributed by Domino Foods, Inc., Yonkers, NY 10705, STORE IN A COOL, DRY PLACEPotential contamination with foreign objects.
- Class I
Food Recall · August 12, 2025
Wegmans Caramel Apple Pecan Topped Brie Cheese -Small - 13 OZ - Clear plastic container with lid UPC: 2-77645-XXXXX-3 (X - varies by weighted price)Products may be contaminated with Listeria monocytogenes
- Class II
Medical Device Recall · August 12, 2025
Siemens Medical Solutions USA, Inc
Artis Pheno. Image-Intensified Flouroscopic X-Ray System.Limited system movements after startup .
- Class II
Medical Device Recall · August 12, 2025
Applied Medical Technology Inc
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 90, REF E NRT-05090-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestiThe nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
- Class II
Food Recall · August 12, 2025
Frozen shrimp in bulk packaging. 20 lbs (10 x 2 lbs blocks); 20 lbs (20 x 1 lbs blocks); 9 lbs case UPC# SH0176; SH0430; SH0320; SH0369; SH0370Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
- Class II
Food Recall · August 12, 2025
Baker's Authority Three Seed Mix; 5lb bag; stored dry at room temperature; packaged in silver bagProduct label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: millet and flax
- Class II
Medical Device Recall · August 12, 2025
Applied Medical Technology Inc
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 90, REF E NRT-06090-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestiThe nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
- Class I
Food Recall · August 12, 2025
Wegmans Grilling Camembert with Tapenade & Roasted Tomatoes - 10 OZ - Overwrapped black and gold metal tray UPC: 2-77297-XXXXX-0 (X - varies by weighted price)Products may be contaminated with Listeria monocytogenes
- Class I
Food Recall · August 12, 2025
Quesito El Establo brand Spanish Cheese QUESITO COLOMBIANO; INGREDIENTS: Milk, Cheese Cultures, Salt, Vitamins C and D; INGREDIENTES: Leche, Cuajo, Sal, Vitaminas C y D; NET WT. 1 LB.; KEEP REFRIGERATProduct was manufactured and held under insanitary conditions. Product may be contaminated with Listeria monocytogenes.
- Class II
Food Recall · August 12, 2025
Baker's Authority Everything Bagel Mix; 5lb bag and 1lb bag; stored dry at room temperature; packaged in silver bagProduct label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: poppy seeds, dried garlic, dried onion, and sea salt
- Class I
Food Recall · August 12, 2025
Wegmans Medium Camembert Soft Ripened Cheese - 8.8oz - Round wooded container; UPC: 2-77467-00000-7 , 0-77890-53515-8Products may be contaminated with Listeria monocytogenes
- Class II
Food Recall · August 12, 2025
Baker's Authority Graham Cracker Meal; 5lb bag; stored dry at room temperature; packaged in silver bagProduct label does not list ingredients including major food allergens: wheat and soy (vegetable oil). Additional undeclared ingredients include: niacin, reduced iron, vitamin B1, vitamin B2, invert sugar
- Class II
Medical Device Recall · August 12, 2025
Applied Medical Technology Inc
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 55, REF E NRT-06055-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestiThe nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
- Class II
Medical Device Recall · August 12, 2025
Applied Medical Technology Inc
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55, REF E NRT-05055-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestiThe nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
- Class II
Medical Device Recall · August 11, 2025
Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The Merge Hemo, Model RCSV2 device is a hemodynamics recording computer system that mMerge Healthcare has been informed by Schiller AG (Baar, Switzerland) of an issue with the Schiller ARGUS PB-3000 Patient Data Module (PDM) where certain units trigger an error message on the Merge Hemo Client ( Pressure Sensor Defective ) during non-invasive blood pressure (NIBP) measurements, specifically when the initial inflation pressure is set in the high-pressure range (>240 mmHg). The ARGUS PB-3000 is a vital signs monitoring instrument intended to be integrated into the Merge Hemo System. No other components of the Merge Hemo System are affected.
- Class II
Medical Device Recall · August 11, 2025
Siemens Healthcare Diagnostics, Inc.
Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP). Material Number: 11097543.Potential for falsely depressed patient, quality control (QC), and/or calibration results or delayed results.
- Class II
Drug Recall · August 11, 2025
Lisdexamfetamine Dimesylate Capsules, 40 mg, 100-count bottles, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC 0527-4664-37Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate Capsules 40mg, contained Lisdexamphetamine Dimesylate Capsules 30mg.
- Class II
Medical Device Recall · August 11, 2025
Agilent Technologies Denmark ApS
Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number: GA60461-2CN Software Version: Not applicable Product Description: FLEX Monoclonal MouTheir is the potential for weak staining which may result in false negative CD20 identification.
- Class I
Food Recall · August 11, 2025
Brie Royal Faucon; Net Weight about: 2.2lb/ 1kg LOT AUS/USProduct may be contaminated with Listeria monocytogenes
- Class II
Medical Device Recall · August 11, 2025
Agilent Technologies Denmark ApS
Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number: GA60461-2 Software Version: Not applicable Product Description: FLEX Monoclonal MouseTheir is the potential for weak staining which may result in false negative CD20 identification.
- Class II
Medical Device Recall · August 11, 2025
Agilent Technologies Denmark ApS
Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number: GA60461-2J Software Version: Not applicable Product Description: FLEX Monoclonal MousTheir is the potential for weak staining which may result in false negative CD20 identification.
- Unclassified
Vehicle Recall · August 10, 2025
2026 BMW R 1300 RTA loss of drive power while riding increases the risk of a crash.
- Unclassified
Vehicle Recall · August 10, 2025
2026 BMW X6Water inside electrical components can cause a loss of headlights or door closing functions, increasing the risk of a crash. In addition, an electrical short circuit may occur, increasing the risk of a fire while parked or driving.
- Class II
Food Recall · August 10, 2025
BISCUIT MIX, SNG 1000042143 NET WEIGHT 2.625 LBS Packed Exclusively For: Chick-fil-A, Inc. 5200 Buffington Road Atlanta, Ga 30349Undeclared eggs
- Unclassified
Vehicle Recall · August 9, 2025
2025 RIVIAN R1T, 2025 RIVIAN R1SFailure to detect another vehicle increases the risk of a crash.
- Class II
Medical Device Recall · August 8, 2025
Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8 m), Product Code REF 2C8519; intravascular administration setBaxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation.
- Class II
Medical Device Recall · August 8, 2025
Greiner Bio-One North America, Inc.
Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2%, REF: 454322Blood collection tubes were manufactured with the label applied too high on the tube, which shifted the printed fill level mark upward, which could result in unnecessary sample rejection and repeat collections.
- Class III
- Class II
Medical Device Recall · August 8, 2025
RayStation with the following product descriptions: 1. RayStation 10B, Software Version: 10.1.0.613. 2. RayStation 10B Service Pack 1, Software Version: 10.1.1.54. Product Description: RadDICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
- Class II
Medical Device Recall · August 8, 2025
Philips Medical Systems Nederland B.V.
IntelliSpace Cardiovascular, Software 8.0.0.4.Software issue that results in the display of outdated information.
- Class II
Medical Device Recall · August 8, 2025
Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.