Lead recalls (page 4)
349 recalls.
- Allura Xper FD20/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 Biplane recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 Biplane recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10F recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Product Name: Allura Xper FD10C recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - MAXXUS recall (GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING)
Medical deviceClass IIReported January 21, 2026 · GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and ... - SMV BodyTrack recall (GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING)
Medical deviceClass IIReported January 21, 2026 · GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and ... - SMV DSI recall (GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING)
Medical deviceClass IIReported January 21, 2026 · GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and ... - SMV DSX New Line recall (GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING)
Medical deviceClass IIReported January 21, 2026 · GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and ... - MAVERICK¿ Measurement Module Spectrometer PN 820-01367 recall (REPLIGEN CORPORATION)
Medical deviceClass IIReported January 21, 2026 · Potential Elevated Laser Output A disconnected cable or a poorly crimped cable under mechanical bending stress can cause loss of electrical contact. At one... - Greatale Recalls Self-Feeding Pillows Due to Risk of Serious Injury or Death from Aspiration and Suffocation
Consumer productReported January 16, 2026 · The recalled self-feeding pillows hold the bottle at an unsafe angle while keeping it fixed in place so the infant cannot pull away. This can lead to... - Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK recall (Medline Industries, LP)
Medical deviceClass IIReported January 14, 2026 · Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and patient... - Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog Number:... recall (IMRIS Imaging Inc)
Medical deviceClass IIReported January 14, 2026 · Torque screw may crack or separate. If used, an affected screw could lead to inadequate head stabilization, compromised surgical precision, procedural delays... - Philips Tempus Pro Patient Monitor recall (Remote Diagnostic Technologies Ltd.)
Medical deviceClass IIReported January 14, 2026 · Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BDR) but ICP and BDR measurements have not been tested or validated for accuracy. If... - Revogene C. difficile recall (Meridian Bioscience Inc)
Medical deviceClass IIReported January 14, 2026 · The affected lots show a decline in performance over time, which may lead to false-negative results. - The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay with... recall (Roche Diagnostics Operations, Inc.)
Medical deviceClass IIReported January 14, 2026 · Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - LifeShield Drug Library Management recall (ICU Medical, Inc.)
Medical deviceClass IIReported December 31, 2025 · For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been completed. Users... - BD Pyxis MedStation ES recall (CareFusion 303, Inc.)
Medical deviceClass IIReported December 31, 2025 · Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a... - Chef brand Milk Pan 24cm recall (Shata Traders Inc.)
FoodClass IIReported December 24, 2025 · Products found to contain leachable lead levels (3.00 mg/L) - Intelerad InteleShare software recall (DICOM Grid, Inc.)
Medical deviceClass IIReported December 24, 2025 · Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are met: Viewing... - Orthofix NorthStar OCT Navigation Surgical Technique Guide recall (SEASPINE ORTHOPEDICS CORPORATION)
Medical deviceClass IIReported December 24, 2025 · The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards as... - Sonex brand aluminum pot recall (Alanwar Food Corp.)
FoodClass IReported December 10, 2025 · Products found to contain leachable lead levels (0.323mg/L)