Safety Recalls
RSS ↗15,364 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 11,201–11,250 of 15,364
- Unclassified
Vehicle Recall · July 3, 2024
2025 INTERNATIONAL LTTurn signals that do not function as intended may confuse other road users, increasing the risk of a crash.
- Class II
Medical Device Recall · July 3, 2024
GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement Configured for Circular Staplers, 25mm; Catalog number: 1BSGC25;Devices were labeled with an expiration date of four years and ten days rather than the validated two years.
- Class II
Medical Device Recall · July 3, 2024
Siemens Medical Solutions USA, Inc
Sensis Vibe systems with software version VD15B in combination with Sensis High End Server -Intended to be used as a diagnostic and administrative tool supporting hemodynamic catheterizations and/or eIf the Sensis documentation functionality is used during adding of once-per-study reporting events (e.g., Type 1 events, as further defined in the administrator manual), the possibility exists that the application could crash.
- Class II
Medical Device Recall · July 3, 2024
Ortho-Clinical Diagnostics, Inc.
VITROS Immunodiagnostic VITROS Folate Reagent Pack 1/2It was confirmed that fibrinogen in patient plasma samples precipitates out of solution upon the addition of folate stabilizer reagent as part of the pre-treatment process causing the increase in "TM5-4MB" condition codes which lead to a delay of results.
- Class II
Medical Device Recall · July 3, 2024
Siemens Medical Solutions USA, Inc
Sensis Vibe systems with software version VD15B in combination with AXIOM Sensis Post Processing Workstation-Intended to be used as a diagnostic and administrative tool supporting hemodynamic cathetIf the Sensis documentation functionality is used during adding of once-per-study reporting events (e.g., Type 1 events, as further defined in the administrator manual), the possibility exists that the application could crash.
- Unclassified
Consumer Product Recall · July 3, 2024
Focusee LTD, of Los Angeles, California
Tideway High-Speed Hair DryersThe handheld hair dryers lack an immersion protection device, posing an electrocution or shock hazard to consumers, if they fall into water when plugged in. The CPSC has determined that hair dryers not equipped with the integral immersion protection present a substantial product hazard.
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Conchas Guatemala packaged in plastic bagUndeclared Allergen - Soy
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Besos packaged in plastic bagUndeclared Allergen - Soy
- Class II
Medical Device Recall · July 2, 2024
Stryker Sustainability Solutions
Disposable 5 Lead Cable and Lead Wire System, 50 inches, REF: LW-309DS50/5ADisposable 5 lead cable and lead wire system package that should contain lead systems, lead telemetry systems and a dual connect cable, may in fact contain, different ECG Leads, which are not approved for reprocessing, but that may have been reprocessed, which may lead to devices not performing as intended.
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Sheca Redonda packaged in plastic bagUndeclared Allergen - Soy
- Class III
Drug Recall · July 2, 2024
Zydus Pharmaceuticals (USA) Inc
Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534Cross contamination with other products
- Class III
Drug Recall · July 2, 2024
Novel Laboratories, Inc. d.b.a Lupin Somerset
PEG-3350, Sodium Sulfate, Sodium Chloride, Potassium Chloride, Sodium Ascorbate, and Ascorbic Acid for Oral Solution 100g/7.5 g /2.691 g/1.015 g/ 5.9 g / 4.7 g, 3 pouches/carton, Rx only, DistributedDefective container: potential for non-sealed pouches which can lead to product leakage.
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Concha Mexicana packaged in plastic bagUndeclared Allergen - Soy
- Class II
Medical Device Recall · July 2, 2024
Siemens Medical Solutions USA, Inc
LUMINOS Lotus Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Number: 11574100The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays
- Class III
Drug Recall · July 2, 2024
Zydus Pharmaceuticals (USA) Inc
Micafungin for injection, USP, 100 mg/vial, Single-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Zydus Lifesciences Ltd., Vadodara, India, NDC 16714-301-0Cross contamination with other products
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Roscas packaged in plastic bagUndeclared Allergen - Soy
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Pegado packaged in plastic bagUndeclared Allergen - Soy
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Casco packaged in plastic bagUndeclared Allergen - Soy
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Curenitos packaged in plastic bagUndeclared Allergen - Soy
- Class III
Drug Recall · July 2, 2024
Zydus Pharmaceuticals (USA) Inc
Verapamil Hydrochloride Injection, USP 10 mg/4 mL (2.5 mg/mL), 5 x 4 mL Single-Dose Vial per carton, Rx Only, Manufactured by: Zydus Lifesciences Ltd. Vadodara, India, Distributed by: Zydus PharmaceutCross contamination with other products.
- Class II
Medical Device Recall · July 2, 2024
Siemens Medical Solutions USA, Inc
Luminos dRF Max- Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762471The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays
- Unclassified
Vehicle Recall · July 2, 2024
2023 LUCID AIR, 2024 LUCID AIRA sudden loss of drive power increases the risk of a crash.
- Class II
Drug Recall · July 2, 2024
SUN PHARMACEUTICAL INDUSTRIES INC
Decitabine for Injection 50mg per vial, For intravenous infusion only Cytotoxic Agent, Sterile, Rx Only, Single-Dose Vial, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, ManuCGMP Deviations: Out of Specification for Total Aerobic Microbial Count (TAMC) test for unfiltered bulk for decitabine for injection.
- Class II
Medical Device Recall · July 2, 2024
Siemens Medical Solutions USA, Inc
Multitom Rax -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Number: 10860700The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays
- Class II
Medical Device Recall · July 2, 2024
BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-03, 360-1580-01, 360-1580-02, 360-1580-03, 360-2080-01, 360-2080-02, 360-2080-03, 370-1080-01, 370-1080-02, 370Holes have been identified in biopsy instrument packaging trays compromising the sterile barrier, which may lead to cross contamination, or the introduction of micro-organisms into the access site, which could lead to an infectious process, bacteremia, or sepsis.
- Class II
Medical Device Recall · July 2, 2024
CPT Hip Joint Metal/Polymer Semi-Constrained Cemented Prosthesis, used in Hip Arthroplasty; Item Numbers 00811400000 00811400010 00811400100 00811400110 00811400200 00811400210 00811400218 0081Affected product has an increased risk of postoperative perisprosthetic femoral fracture (PFF). The IFU is being updated to reflect the risk of PFF.
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Sheca Anis packaged in plastic bagUndeclared Allergen - Soy
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Cortado Rojo packaged in plastic bagUndeclared Allergen - Soy
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Gusano packaged in plastic bagUndeclared Allergen - Soy
- Unclassified
Vehicle Recall · July 2, 2024
2024 KIA TELLURIDEA loss of drive power increases the risk of a crash. A hole in the engine block increases the risk of a fire.
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Corona packaged in plastic bagUndeclared Allergen - Soy
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Liso packaged in plastic bagUndeclared Allergen - Soy
- Class III
Drug Recall · July 2, 2024
Zydus Pharmaceuticals (USA) Inc
Verapamil Hydrochloride Injection, USP 5 mg / 2mL(2.5 mg/mL), packaged as (a) 25x2 mL Single-Dose Vial per carton, Vial NDC: 70710-1643-1; Carton NDC 70710-1643-7; (b) 5x2 mL Single-Dose Vial per cartCross contamination with other products.
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Champurradas packaged in plastic bagUndeclared Allergen - Soy
- Class II
Food Recall · July 2, 2024
Panaderia Guatemex - Churros packaged in plastic bagUndeclared Allergen - Soy
- Class II
Medical Device Recall · July 2, 2024
Siemens Medical Solutions USA, Inc
Luminos Agile Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762472The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays
- Class III
Food Recall · July 1, 2024
Lush Lavender & Wildberry Spritz is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well RefFirm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
- Class II
Medical Device Recall · July 1, 2024
Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the following Reference numbers: United States: BXB055902C, BXB063902C, BXB065902C, BXB067902C, BXB073902C, BXB075902C, BXB077902CDue to packaging defects, sterility assurance and heparin activity may be compromised.
- Class III
Food Recall · July 1, 2024
Tropical Blackberry is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated AftFirm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
- Class III
Food Recall · July 1, 2024
Sunkissed Lavender and Lemon is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well RefrigeFirm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
- Class III
Food Recall · July 1, 2024
Life s a Peach Spritzer is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well RefrigeratedFirm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
- Class II
Food Recall · July 1, 2024
Abby's Best BISCUIT MIX NET WEIGHT 4 LBS. 8 OZ. (2.04 KG) INGREDIENTS: ENRICHED BLEACHED FLOUR***PARTIALLY HYDROGENATED VEGETABLE SHORTENING (CONTAINS SOYBEAN OIL) WITH EMULSIFIER***LEAVENING***BUTTERDuring an inspection by the SCDA the firm was notified that their label does not declare the allergen wheat.
- Class III
Food Recall · July 1, 2024
Spicy Orange and Mango Fusion is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well RefrigFirm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
- Class III
Food Recall · July 1, 2024
Blackberry and Lime Mixer is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well RefrigeratFirm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
- Class III
Food Recall · July 1, 2024
Keep It Spicy Pear & Jalapeno Mixer is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake WellFirm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
- Class II
Medical Device Recall · July 1, 2024
Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the following Reference numbers: United States: BXB051501A BXB051502A BXB051901A BXB051902A BXB052901A BXB052902A BXB053901A BXB0Due to packaging defects, sterility assurance and heparin activity may be compromised.
- Class II
Medical Device Recall · July 1, 2024
Olympus Corporation of the Americas
The Everest Bipolar Cutting Forceps are intended to be passed through a 5-mm or 10-mm cannula, depending on the model/outer diameter size of the forceps. Coagulation is achieved using electrosurgicalFractures and breakages in packaging trays and Tyvek covers, which may result in a sterility breach
- Class II
Medical Device Recall · July 1, 2024
Olympus Corporation of the Americas
The Everest Bipolar Cutting Forceps are intended to be passed through a 5-mm or 10-mm cannula, depending on the model/outer diameter size of the forceps. Coagulation is achieved using electrosurgicalFractures and breakages in packaging trays and Tyvek covers, which may result in a sterility breach
- Class III
Food Recall · July 1, 2024
Brown Sugar Simple Syrup is a non-alcoholic cocktail mixer. Product is packaged in glass 5oz. bottle and sold under brand Urban River Spirits.Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.