Safety Recalls

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15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

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Showing 7,251–7,300 of 15,271

Medical Device Recall · April 3, 2025
Waldemar Link GmbH & Co. KG (Mfg Site)
Tibial Augment; Item Numbers: (1) 880-331/11 (Sz. 1-2 - cemented x-sm), (2) 880-331/12 (Sz. 1-2 - cemented sm), (3) 880-331/13 (Sz. 1-2 - cemented md), (4) 880-331/21 (Sz. 1-2 - cemented lg), (5) 880-
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
Class II
Food Recall · April 3, 2025
Supherb Farms
Label: FROZEN CHOPPED CILANTRO; PACK SIZE: 4 - 8 oz; NET WT: 2 lb; PERISHABLE - KEEP FROZEN; Packaging: 4 - 8 oz ziploc plastic bags in a white cardboard box; Net Wt. 2 lb
Potential contamination with foreign objects.
Class II
Medical Device Recall · April 3, 2025
Medtronic Neuromodulation
Enhanced Verify Evaluation Handset (CFN HH90130FA)
Evaluation handsets may not be able to communicate with the neurostimulator due to handsets having a faster processing speed than prior handsets. An inability to connect may cause the therapy to stop being delivered and a system error will be displayed. Patient may experience return of underlying disease symptoms (e.g. overactive bladder, urinary retention, or fecal incontinence) based on their response to stimulation during the evaluation period.
Class II
Medical Device Recall · April 3, 2025
Waldemar Link GmbH & Co. KG (Mfg Site)
Distal Femoral Augment; Item Numbers: (1) 880-300/11 (Sz. 0 - cemented sm), (2) 880-300/21 (Sz. 0 - cemented lg), (3) 880-301/11 (Sz. 1-2 - cemented sm), (4) 880-301/21 (Sz. 1-2 - cemented lg), (5) 88
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
Class II
Consumer Product Recall · April 3, 2025
Enerco Group Inc., of Cleveland, Ohio
DEWALT 70,000 BTU Outdoor Portable Cordless Forced Air Propane Heaters
The recalled portable heaters' operating instructions can cause consumers to incorrectly depress the start button too quickly and prevent the fan from starting, causing the heaters to overheat, posing fire and burn hazards.
Unclassified
Consumer Product Recall · April 3, 2025
AliExpress, of San Mateo, California
LVOE Hair Dryers
The handheld hair dryers lack an immersion protection device and can cause death or serious injury due to electrocution or shock if they fall into water when plugged in. The hair dryers are in violation of the federal regulations and present a substantial product hazard.
Unclassified
Consumer Product Recall · April 3, 2025
AliExpress, of San Mateo, California
Mini Travel Hair Dryers
The handheld hair dryers lack an immersion protection device and can cause death or serious injury due to electrocution or shock if the hair dryers fall into water when plugged in. The hair dryers are in violation of the federal regulations and present a substantial product hazard.
Unclassified
Consumer Product Recall · April 3, 2025
Amesbury Industries Inc., d/b/a AmesburyTruth, of Houston, Texas
Ashland 10-inch and 14-inch two-bar casement window hinge tracks
The metal sliding arm can disengage from the hinge track causing the window sash to fall, posing an impact injury hazard to consumers.
Unclassified
Consumer Product Recall · April 3, 2025
1616 Holdings Inc., of Philadelphia, Pennsylvania
Room2Room LED Iridescent Bear Lights
The power switch on the USB cord can overheat and melt, posing fire and burn hazards.
Unclassified
Consumer Product Recall · April 3, 2025
Sakar International Inc., of Edison, New Jersey
Vivitar Blender Bottles
The blender's blades can continue to operate when the bottle is not attached to the blender, posing a laceration hazard.
Unclassified
Consumer Product Recall · April 3, 2025
Polaris Industries Inc., of Medina, Minnesota
Model Year 2022-2025 RZR Pro R and RZR Pro R 4 Recreational Off-Road Vehicles (ROVs)
The fasteners on the vehicle's rollover protective structure (ROPS) pillar joints can be missing or loose and fail to protect the occupants, if the vehicle rolls over or tips over. This poses an injury hazard.
Unclassified
Medical Device Recall · April 2, 2025
Preat Corp
Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arc
Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant.
Class II
Drug Recall · April 2, 2025
Amerisource Health Services LLC
Haloperidol Decanoate Injection, 50mg/mL* , 1 mL Single-Dose Vial, Rx only, Manufactured by Somerset Therapeutics Limited, 54/1, Boodhihal Village, Nelamangala, Bangalore - 562123, Karnataka, India, M
Lack of assurance of sterility. Bacterial contamination detected in some media fill units
Class II
Drug Recall · April 2, 2025
Amerisource Health Services LLC
Haloperidol Decanoate Injection, 100mg/mL*, 5 x 1 mL Single-Dose Vials, Rx Only, Manufactured by: Somerset Therapeutics Limited, #54/1 Boodhihal Village, Nelamangala, Bangalore -562123, Karnataka, In
Lack of assurance of sterility. Bacterial contamination detected in some media fill units
Class II
Drug Recall · April 2, 2025
Amerisource Health Services LLC
Haloperidol Decanoate Injection, 100 mg/mL*, 1 x 1 mL Single-Dose Vial, Rx only, Manufactured by: Somerset Therapeutics Limited, #54/1, Boodhihal Village, Nelamangala, Bangalore - 562123, Karnataka,
Lack of assurance of sterility. Bacterial contamination detected in some media fill units
Class II
Medical Device Recall · April 2, 2025
Leica Biosystems Melbourne Pty Ltd
HistoCore PELORIS 3, Model/Catalog Number: 45.0005/45.7512.501 A11, Software Version: 3.4.0. The HistoCore PELORIS 3 Rapid Tissue Processor is a dual retort rapid tissue processor used to prepare tis
There is a leakage issue associated with the tubing in the manifold of the instrument.
Class II
Medical Device Recall · April 2, 2025
Getinge Disinfection Ab
Washer Disinfector Aquadis 56; Model Number: 56M
The frequency inverter is not programmed by supplier according to specification which causes the circulation pump to start earlier than expected, resulting in additional wear and tear, earlier than expected, on the axial seal in the pump housing.
Class II
Food Recall · April 2, 2025
Caraluzzi's Markets
Caraluzzi's Italian Style Seafood Burgers, 8oz; INGREDIENTS: Cod, Salmon, Shrimp, Scallops, Onions, Olive Oil, White Wine, Parsley, Sodium Caseinate (A Milk Derivative), Spices, Garlic, Salt, Paprika,
Product contains undeclared egg.
Class I
Medical Device Recall · April 2, 2025
Getinge Disinfection Ab
Washer Disinfector Aquadis 56; Model Number: 56A
The frequency inverter is not programmed by supplier according to specification which causes the circulation pump to start earlier than expected, resulting in additional wear and tear, earlier than expected, on the axial seal in the pump housing.
Class II
Food Recall · April 1, 2025
TONY'S CHOCOLONELY INC
Tony's Chocolonely Dark Chocolate Almond Sea Salt
Contains foreign objects (stones)
Class II
Medical Device Recall · April 1, 2025
IBA Dosimetry GmbH
myQA iON; Article Number: MQ10-000;
Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character.
Class II
Food Recall · April 1, 2025
TONY'S CHOCOLONELY INC
Tony's Chocolonely Everything Bar
Contains foreign objects (stones)
Class II
Food Recall · April 1, 2025
Dr. Praeger's Sensible Foods Inc.
Dr. Praeger s California Veggie Fries 8oz,
Undeclared Allergen (Soy)
Class II
Food Recall · April 1, 2025
Panaderia Salvadorena Ii
PANADERIA/BAKERY Salvadorena; Quesadilla de Queso; Ingredients: Rice, Wheat Flour, soy, eggs, sugar, butter, baking powder, salt, water, sour cream, sesame seeds; UPC 0 21651 16499 6; NET WEIGHT APPRO
Product contains undeclared milk.
Class II
Medical Device Recall · April 1, 2025
Philips North America Llc
Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.
Unintended motion issues related to Interventional Control that may lead to collision of the Gantry/table with the operator or patient.
Class II
Medical Device Recall · March 31, 2025
Siemens Healthcare Diagnostics Inc
Stratus CS Acute Care cTNI TestPak.IVD test for cardiac troponin I in heparinized plasma.
Siemens Healthcare Diagnostics Inc., is recalling their Stratus CS Acute Care cTNI TestPak, an IVD test for cardiac troponin I in heparinized plasma by removal. The reason for the recall is an increased occurrence of random non-repeatable false positive cardiac Troponin l(cTnI) results at any point during the TestPaks shelf life when using the Stratus CS cTnI Acute Care Testpak.
Class II
Medical Device Recall · March 31, 2025
Belmont Instrument LLC
Straight Inflow/Outflow Patient Line Kit. Model Number: 902-00037. Sterile, single-use, disposable set used with the Hyperthermia Pump. The Straight Inflow/Outflow Patient Line Kit (P/N 902-0003
Potential crack in the female connector located on the Heat Exchanger in the set, which will lead to a fluid leak through the crack during priming of the rapid infuser.
Class II
Drug Recall · March 31, 2025
Medisca Inc.
Bimatoprost powder, Bulk Ingredient, a) 5g (NDC 38779-3066-03), b) 1g (NDC 38779-3066-06), c) 1g (NDC 38779-3066-09) drums, Medisca, Plattsburgh, NY
CGMP Deviations
Class II
Medical Device Recall · March 31, 2025
AVID Medical, Inc.
Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
Class II
Drug Recall · March 31, 2025
Denver Solutions, LLC DBA Leiters Health
Rocuronium Bromide 50 mg per 5mL (10mg per mL), 5mL Single Dose Syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC: 71449-004-11
Lack of Assurance of Sterility: Leaking/damaged syringes.
Class II
Medical Device Recall · March 31, 2025
AVID Medical, Inc.
Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit.
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
Class II
Drug Recall · March 31, 2025
Denver Solutions, LLC DBA Leiters Health
PHENYLephrine HCl in 0.9% Sodium Chloride, 0.5 mg per 5mL (100 mcg/mL), 5 mL Single Dose Syringe, Rx Only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC: 71449-001-11,
Lack of Assurance of Sterility: Leaking/damaged syringes.
Class II
Drug Recall · March 31, 2025
Denver Solutions, LLC DBA Leiters Health
dexmedeTOMIDine HCl PF, in 0.9% Sodium Chloride, 20 mcg (base) per 5mL, (4 mcg (base) per mL), 5mL Single Dose syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112, NDC: 71449-131
Lack of Assurance of Sterility: Leaking/damaged syringes.
Class II
Medical Device Recall · March 31, 2025
AVID Medical, Inc.
Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
Class II
Drug Recall · March 31, 2025
B. Braun Medical Inc
0.9% Sodium chloride Irrigation USP, Isotonic Solution for Irrigation, 500 mL Plastic Irrigation Container (PIC), B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-2201-10
Presence of Particulate Matter
Class II
Drug Recall · March 31, 2025
Denver Solutions, LLC DBA Leiters Health
Ketamine HCl 50mg per 5mL (10 mg per mL), 5mL Single Dose Syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112.NDC: 71449-068-11
Lack of Assurance of Sterility: Leaking/damaged syringes.
Class II
Drug Recall · March 31, 2025
Denver Solutions, LLC DBA Leiters Health
Glycopyrrolate, 1mg per 5mL, (0.2 mg/mL), Single Dose 5 mL syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC 71449-104-11
Lack of Assurance of Sterility: Leaking/damaged syringes.
Class II
Medical Device Recall · March 31, 2025
Belmont Instrument LLC
3.0 Liter Disposable Set (4 sets/case). Model Number: 903-00032. The P/N 903-00032 consists of 4 Large Volume Reservoirs (P/N 903-00018) and 4 Heat Exchanger/Patient Line set (P/N 403-00382). Th
Potential crack in the female connector located on the Heat Exchanger/patient line set, which will lead to a fluid leak through the crack during priming of the Rapid Infuser.
Class II
Medical Device Recall · March 31, 2025
Belmont Instrument LLC
Straight Inflow/Bifurcated Outflow Line Kit. Model Number: 902-00038. Sterile, single-use, disposable set used with the Hyperthermia Pump. The Straight Inflow/Outflow Patient Line Kit (P/N 902-0
Potential crack in the female connector located on the Heat Exchanger in the set, which will lead to a fluid leak through the crack during priming of the rapid infuser.
Class II
Medical Device Recall · March 31, 2025
Ultra Clean Systems, Inc.
Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72 Model Number 6003000805 Ultrasonic cleaning system
During routine preventative maintenance checks, it was revealed that carbon filter sensors were breaking down due to electrochemical degradation.
Class II
Medical Device Recall · March 31, 2025
Belmont Instrument LLC
Hyperthermia Pump Procedure Kit. Model Number: 902-00045. Sterile, single-use, disposable set used with the Hyperthermia Pump. The Hyperthermia Procedure kit (P/N 902-00045) consists of 4.4 Lite
Potential crack in the female connector located on the Heat Exchanger in the set, which will lead to a fluid leak through the crack during priming of the rapid infuser.
Class II
Food Recall · March 29, 2025
Knockroe Inc
Bonya Vanilla Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Undeclared Almonds
Class I
Food Recall · March 29, 2025
Knockroe Inc
Bonya Raspberry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Undeclared Almonds
Class I
Food Recall · March 29, 2025
Knockroe Inc
Bonya Peach Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Undeclared Almonds
Class I
Food Recall · March 29, 2025
NRC Nutrition Pty Ltd
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
inconsistent blending of iodine in the product
Class II
Food Recall · March 29, 2025
Knockroe Inc
Bonya Blueberry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Undeclared Almonds
Class I
Food Recall · March 29, 2025
Knockroe Inc
Bonya Lemon Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Undeclared Almonds
Class I
Food Recall · March 29, 2025
Knockroe Inc
Bonya Passion Fruit Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Undeclared Almonds
Class I
Food Recall · March 29, 2025
Knockroe Inc
Bonya Coconut Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Undeclared Almonds
Class I
Food Recall · March 29, 2025
Knockroe Inc
Bonya Pineapple Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Undeclared Almonds
Class I