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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
August 6, 2025Medical DevicesFDA
Boston Foundation For Sight recalls BostonSight PROSE Lens.
Hazard: Select orders of lenses were manufactured with errors impacting sagittal height, haptics, or both.
August 6, 2025Medical DevicesFDA
Boston Foundation For Sight recalls BostonSight SCLERAL Lens
Hazard: Select orders of lenses were manufactured with errors impacting sagittal height, haptics, or both.
August 6, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura R8.2.x Systems. Software Verion: R8.2.x. 1. Allura Xper FD10, Model Number: 722026. 2. Allura Xper
Hazard: Potential for temporary loss of imaging (X-ray) functionality due to software issue.
August 6, 2025Medical DevicesFDA
MICROVENTION INC. recalls LIFEPEARL Drug Elutable Microspheres: 200 +/- 50 micrometers, REF: 8LP2S200; 400 +/- 50 micrometers, REF: 8LP2S400
Hazard: Drug Elutable Microspheres have a smaller actual average diameter that is not within specification, which may lead to inability to reach the desired treatment location (non-targeted embolization), additional procedure/treatment required, blockage other than target vessel, increased procedure time, incomplete embolization, and/or inability to treat the patient.
August 6, 2025Medical DevicesFDA
Steris Corporation recalls Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR E-Series Surgical Lighting Systems
Hazard: The DFPM yoke assembly ("yoke assembly") may detach from the spring arm. Should the yoke assembly detach from the spring arm, the yoke assembly would not be expected to fully detach but rather hang from the wiring within the yoke assembly.
August 6, 2025Medical DevicesFDA
Steris Corporation recalls Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR A-Series Surgical Lighting Systems
Hazard: The DFPM yoke assembly ("yoke assembly") may detach from the spring arm. Should the yoke assembly detach from the spring arm, the yoke assembly would not be expected to fully detach but rather hang from the wiring within the yoke assembly.
August 6, 2025Medical DevicesFDA
Remote Diagnostic Technologies Ltd. recalls Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an ac
Hazard: Kit USB flash drive contains outdated software, which could result in reverting patient monitor to outdated software and reintroducing the video laryngoscope issue (related to an August 2023 recall), which could lead to delay in diagnosis, delayed treatment, hypoxia due to unexpected loss of video laryngoscopy and all other monitor measurements during system restart.
August 6, 2025Medical DevicesFDA
HeartSine Technologies Ltd recalls HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The HeartSine samaritan¿ PAD (Public Access Defibr
Hazard: Due to a component manufacturing issue, Automated External Defibrillator may not function properly (deliver shocks)
August 6, 2025Medical DevicesFDA
Implant Direct Sybron Manufacturing LLC recalls The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to store, sterilize, verify Drill Stop leng
Hazard: The Drill stop kit contains incorrect components.
August 6, 2025Medical DevicesFDA
Hamilton Medical AG recalls Breathing circuit set, coaxial, 1.80 m, with flow sensor and expiratory valve set, REF: 260128, used with HAMILTON-C1, H
Hazard: Ventilator coaxial breathing circuit may have a crack in blue tubing, which is used to deliver fresh gas to the patient. The crack will compromise inspiratory and expiratory flows, leading to partial or complete rebreathing of exhaled gases, which could lead to acute hypercapnia, respiratory acidosis, and if unrecognized organ dysfunction.
August 6, 2025Medical DevicesFDA
Abiomed, Inc. recalls Automated Impella Controller (AIC), used in left heart support blood pump, including the following: 1. Impella Contr
Hazard: A potential issue with the Automated Impella Controller (AIC) not detecting an Impella pump when it is connected
August 6, 2025Medical DevicesFDA
Draeger, Inc. recalls SafeStar 60A Plus Filter. Bidirectionally breathing system filter.
Hazard: Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
August 6, 2025Medical DevicesFDA
Draeger, Inc. recalls HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter.
Hazard: Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
August 6, 2025Medical DevicesFDA
Draeger, Inc. recalls SafeStar 55 Plus Filter. Bidirectionally breathing system filter.
Hazard: Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
August 6, 2025Medical DevicesFDA
Draeger, Inc. recalls SafeStar 90 Plus Filter. Bidirectionally breathing system filter.
Hazard: Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
August 6, 2025Medical DevicesFDA
Apic Yamada America recalls Molding Equipment. WCM series. Model WCM-330GL-i
Hazard: Apic Yamada has recently discovered that certain products may be out of compliance with FDA electronic product regulations in that they did not bear a required label.
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds E54564-BREADER X5-NET WT 25LBS
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds B90737-BREADER X1-NET WT 25LBS
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds B6AAK3-BREAD CRUMBS X1-NET WT 35LBS
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds B6229J-PIZZA CRISP-NET WT 35LBS
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds B62262-BREAD CRUMBS X1-NET WT 1200 LBS
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds B61672--BREAD CRUMBS X1-NET WT 35 LBS.
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds B61610-BREAD CRUMBS X1-NET WT 45 LBS
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds B61453-BREAD CRUMBS X1-NET WT 25 LBS
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds B60960-BREAD CRUMBS X1-NET WT 6 LBS
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds B6047J-BREAD CRUMBS-NET WT 35 LBS.
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds B6010J BREAD CRUMBS-NET WT 35 LBS
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds B57569 BREADER X1- NEW WT 25 LBS.
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds A93060 BREADER X1- NEW WT 40 LBS.
Hazard: potential Listeria Monocytogenes Contamination
August 6, 2025Food & BeverageFDA
Newly Weds Foods, Inc. recalls Newly Weds A60647- BREAD CRUMBS X1-NET WT 35 LBS.
Hazard: potential Listeria Monocytogenes Contamination