Safety Recalls

15,362 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 8,401–8,450 of 15,362

• Food Recall · January 15, 2025

  Mutual Trading Company Inc.

  Product is individually packaged in opaque airtight plastic packaging with Chinese lettering on one side. Opposite side contains English label that reads: #61122; ANKIMOBO (prepared Monkfish Liver) I

  Imported Monkfish Liver undeclared allergen (Milk)

  Class I

• Medical Device Recall · January 15, 2025

  Philips North America Llc

  IntelliVue Patient Monitor MX400. Model Number: 866060

  Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

  Class II

• Food Recall · January 15, 2025

  The Candy Basket Inc

  Lemon Jelly Sticks DARK, item number CB750-D, is packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases from c

  Undeclared Yellow #5 and Potassium Sorbate.

  Class II

• Medical Device Recall · January 15, 2025

  Philips North America Llc

  IntelliVue Patient Monitor MX450. Model Number: 866062

  Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

  Class II

• Food Recall · January 15, 2025

  The Candy Basket Inc

  Marionberry Jelly Sticks MILK, item number CB745-M, is packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases

  Undeclared Red #3, Blue #1, Potassium Sorbate, and Propylene Glycol.

  Class III

• Medical Device Recall · January 15, 2025

  DeRoyal Industries Inc

  DeRoyal AMG Suction Connector Tubing REF: 71-2083, 71-C506, 71-C510, 71-C512, 71-C520, Tubing is intended for fluid movement

  The tubing may not ensure that the yankauer stays intact, and secure to the tubing / yankauer connection for a tight seal. This could result in inadequate suction and cause delay in patient care.

  Class II

• Medical Device Recall · January 15, 2025

  Elekta, Inc.

  MOSAIQ Oncology Information System

  Image offsets calculated by oncology Information System software may be incorrect for Linear Accelerator (LINACs) not characterized at IEC61217 scale.

  Class II

• Medical Device Recall · January 15, 2025

  Philips North America Llc

  IntelliVue Patient Monitor MX500. Model Number: 866064

  Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

  Class II

• Medical Device Recall · January 15, 2025

  Getinge Usa Sales Inc

  Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i C20, Flow-i C30, Flow-i C40, Flow-c, Flow-e. For use during anesthesia.

  Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of respiratory tract, which in worst case may lead to lung edema and/or severe hypocalcemia, blistering, superficial ulceration, and/or hypomagnesemia.

  Class I

• Food Recall · January 14, 2025

  Frito-Lay, Inc. Headquarters

  Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 65040 BBD SEP 13 25 P

  Undeclared milk allergen

  Class I

• Medical Device Recall · January 14, 2025

  Draeger Medical Systems, Inc.

  Infinity Central Station. Model Number: MS26800 The Infinity CentralStation (ICS) is intended for centralized monitoring of adult, pediatric and neonatal patient data within the hospital or clinica

  Edifier speakers (shipped in or after April 2023) may not annunciate when configured in analog mode which can lead to delayed treatment to the patient.

  Class II

• Food Recall · January 14, 2025

  Target Corporation

  Nestle Toll House Valentine's Chocolate Chip cookie dough, Makes 20 cookies. Net wt 14 oz. UPC 0 28000-34408 5. Distributed by Nestle USA, Arlington, VA 22209.

  Improper storage temperature.

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura Xper FD10C; Catalog number: 722001

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 3 M12; Catalog numbers: (1) 722063, (2) 722221.

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Food Recall · January 13, 2025

  Monkey Spit

  Monkey Spit "Monkey Mop" BBQ Sauce, 12 fl oz (355ml) glass bottle, 12 bottles/case; Refrigerate after opening; Manufactured by Smith House MFG. 146-A S. Thompson Ave. Nipomo, CA 93444 (805)619-7959 Mo

  Barbeque sauce product contains undeclared listing of (Milk) in product ingredient listing from sub-ingredient Butter.

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura Xper FD20/20; Catalog numbers: 722038

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Cardio Vascular-Allura Centron; Catalog number: 722400 (OUS ONLY).

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 7 B12; Catalog numbers: (1) 722067, (2) 722225, (3) 722235 (OUS ONLY).

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 7 M12; Catalog numbers: (1) 722078, (2) 722223, (3) 722233 (OUS ONLY).

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 5 M20; Catalog numbers: (1) 722228, (2) 722232 (OUS ONLY), (3) 722281 (OUS ONLY).

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Drug Recall · January 13, 2025

  The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

  Duloxetine Delayed-Release Capsules USP, 20 mg, packaged in a) 30 Unit Doses (3x10 blister packs) NDC 0904-7043-04 and b) 100 Unit Doses (10x10 blister packs) NDC 0904-7043-61, Rx only, Packaged and D

  CGMP Deviations: presence of Nitrosamine Drug Substances Related Impurity (NDSRI), N-Nitroso-Duloxetine above the FDA recommended acceptable intake limit

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura Xper FD20/10; Catalog numbers: 722029

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura Xper FD20 OR Table; Catalog numbers: (1) 722023, (2) 722035.

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura CV20; Catalog numbers: 722031

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026,

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura Xper FD10/10; Catalog numbers: (1) 722005, (2) 722011, (3) 722027.

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura Xper FD20 Biplane; Catalog numbers: (1) 722008, (2) 722013.

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura Xper FD10C System Code: (1) 722001

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Food Recall · January 13, 2025

  Monkey Spit

  Monkey Spit "Atomic Mop" BBQ Sauce, 12 fl oz (355ml) glass bottle, 12 bottles/case; Refrigerate after opening; Manufactured by Smith House MFG. 146-A S. Thompson Ave. Nipomo, CA 93444 (805) 619-7959;

  Barbeque sauce product contains undeclared allergen listing of (Milk) in product ingredient listing from sub-ingredient Butter.

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 3 M12 System Code: (1) 722063 (2) 722221

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Food Recall · January 13, 2025

  Monkey Spit

  Monkey Spit "Swamp Mop" BBQ Sauce, 12 fl oz (355ml) glass bottle, 12 bottles/case; Refrigerate after opening; Monkey Spit, LLC, Tepusquet Cyn Santa Maria, CA 93454; Manufactured by Smith House MFG. 14

  Barbeque sauce product contains undeclared allergens (soy) contained in sub-ingredient

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 3 M15; Catalog numbers: (1) 722064, (2) 722222 (3) 722280(OUS ONLY).

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura CV20 System Code: 722031

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028.

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura Xper FD20 Biplane OR Table; Catalog numbers: (1) 722020, (2) 722025.

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  AlluraXperFD20/10 System Code: (1) 722029

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Allura Xper FD20/15; Catalog numbers: 722058

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) 722234 (4) 722282 System Code: (1) 722078 (2) 722223 (3) 722233

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 5 M12; Catalog numbers: (1) 722227, (2) 722231 (OUS ONLY).

  Possibility of the patient falling from the table related to the mattress used on the patient table.

  Class I

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  AlluraXperFD20/15 System Code: (1) 722058

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II

• Medical Device Recall · January 13, 2025

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 5 M12 System Code: (1) 722227 (2) 722231

  Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

  Class II