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Consumer Product Recalls
127,502 recalls from the U.S. Consumer Product Safety Commission, newest first.
January 29, 2025Medical DevicesFDA
Becton Dickinson & Co. recalls BD PCR Cartridges used with MAX System. Model Number: 437519
Hazard: Potential for signal drift in specific lots of BD PCR Cartridges.
January 29, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: Thunderbeat, 5MM, 35CM, Front-
Hazard: The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
January 29, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,20 cm, Front-
Hazard: The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
January 29, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,20 cm, Front-
Hazard: The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
January 29, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,45 cm,Front-a
Hazard: The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
January 29, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,45 cm,Front-a
Hazard: The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
January 29, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,45 cm,Front-a
Hazard: The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
January 29, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,35 cm ,Front-
Hazard: The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
January 29, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,35 cm, Front-
Hazard: The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
January 29, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,20 cm, Front-
Hazard: The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
January 29, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: Thunderbeat Front-Actuated Gri
Hazard: The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
January 29, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm, 35 cm, Front
Hazard: The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
January 29, 2025Medical DevicesFDA
MICROVENTION INC. recalls Microvention, Headway" 17 Advanced Straight Microcatheter with Hydrophilic Coating, REF: MC172150SX-CN, Sterile R, Rx On
Hazard: Sterility assurance; microcatheter inner packaging may contain incomplete seal.
January 29, 2025Medical DevicesFDA
St. Jude Medical recalls CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Hosptial Electronics System (PES) REF CM3000 Merlin.n
Hazard: As a result of a cloud data migration of Patient and Hospital Electronic Systems (PES and HES) reverted to an outdated configuration causing incorrect/inaccurate pulmonary artery (PA) pressure readings.
January 29, 2025Medical DevicesFDA
St. Jude Medical recalls CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Patient Electronics System (PES) REF CM1100 Merlin.ne
Hazard: As a result of a cloud data migration of Patient and Hospital Electronic Systems (PES and HES) reverted to an outdated configuration causing incorrect/inaccurate pulmonary artery (PA) pressure readings.
January 29, 2025Medical DevicesFDA
St. Jude Medical recalls Merlin.net Patient Care Network (PCN) Heart Failure Web Application (Model MN6000) (Which interfaces with CardioMEMS" H
Hazard: Due to a data migration from on-premises server to the cloud environment, some customers reported that they were not able to transmit readings.
January 29, 2025Medical DevicesFDA
Medtronic Perfusion Systems recalls Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
Hazard: Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
January 29, 2025Medical DevicesFDA
Medtronic Perfusion Systems recalls EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
Hazard: Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
January 29, 2025Medical DevicesFDA
Medtronic Perfusion Systems recalls DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr)
Hazard: Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
January 29, 2025Medical DevicesFDA
O&M HALYARD, INC. recalls Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product Descript
Hazard: Elevated residues of anti-block/slip additive used in manufacturing found within sterile packaging.
January 29, 2025Medical DevicesFDA
Stryker Corporation recalls stryker 3.0MM Precision Neuro Match Head, REF 5820-107-530, used to cut bone and bone cement during neurosurgery
Hazard: There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).
January 29, 2025Medical DevicesFDA
Stryker Corporation recalls stryker 3.0MM Neuro Match Head, REF 5820-107-430, used to cut bone and bone cement during neurosurgery
Hazard: There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).
January 29, 2025Medical DevicesFDA
Stryker Corporation recalls The 3.0MM Neuro Match Head Soft Touch bur (5820-107-030) is intended to be used to cut bone and bone cement during neuro
Hazard: There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-030 but package contains a 5820-107-530 device).
January 29, 2025Medical DevicesFDA
Integra LifeSciences Corp. recalls CODMAN CERTAS Plus Programmable Valve Right Angle Valve Only. Model Number: 828820. Implantable device that provides
Hazard: Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
January 29, 2025Medical DevicesFDA
Integra LifeSciences Corp. recalls CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810PL. Implantable device that provid
Hazard: Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
January 29, 2025Medical DevicesFDA
Integra LifeSciences Corp. recalls CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810 Implantable device that provides
Hazard: Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
January 29, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis Med 4000 Auxiliary (AUX), REF 314
Hazard: Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
January 29, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis Med ES Auxiliary (AUX), REF 343
Hazard: Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
January 29, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis MedStation 4000 AUX, REF 306
Hazard: Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
January 29, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis MedStation 4000 Main, REF 303
Hazard: Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,