Recalls published in April 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in April 2026, newest first.
-
Class II · 7 months ago
Civco Medical Instruments Co. Inc. eTRAX Needle System Starter Kit 12G recall: There was an error in inspection and programming of the eTRAX needle sensor
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip…
-
Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD10/10 recall: Philips has identified instances where X-ray imaging may not be initiated
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
-
Class II · 7 months ago
Medtronic MiniMed, Inc. MiniMed 770G Insulin Pump recall: All Medtronic MiniMed infusion pumps (Paradigm series, 600 series
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and…
-
Class II · 7 months ago
Intuitive Surgical, Inc. Brand Name: da Vinci S, Si Double Fenestrated Grasper recall: Due to increased complaints for broken/frayed grip cables for reusable
Due to increased complaints for broken/frayed grip cables for reusable instruments.
-
Class II · 7 months ago
Medline Industries, LP Sterile Radiology Procedure Kits recall: There is a potential breach in the sterile pouch packaging for one lot
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
-
Class II · 7 months ago
Summa Therapeutics, LLC Brand Name: Finesse BTK Multicath Product Name: Injectable recall: Potential for the balloon in the device to not meet burst specifications
Potential for the balloon in the device to not meet burst specifications.
-
Class II · 7 months ago
Brand Name: Olympus Soltive Pro SuperPulsed Laser System Product Name recall: Following a complaint investigation, Olympus identified a potential defect
Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause…
-
Class II · 7 months ago
Medline convenience kits containing Olympus biopsy valves: 1. Bronch recall: Kits contain recalled Olympus biopsy valves. Olympus is investigating
Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the…
-
Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/20 OR Table recall: Philips has identified instances where X-ray imaging may not be initiated
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
-
Class I · 7 months ago
Philips Respironics Trilogy EV300, Software Version 1.05.15.00 recall: In some situations, the Obstruction Alarm does not trigger within
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
-
Class I · 7 months ago
Baxter Healthcare Corporation Blue Ventilator Adapter Module recall: Urgent Medical Device Correction for the Volara system single-patient use
Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of…
-
Class II · 7 months ago
Philips Medical Systems Nederland B.v. Azurion 5 M20 recall: Philips has identified instances where X-ray imaging may not be initiated
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
-
Class II · 7 months ago
Civco Medical Instruments Co. Inc. eTRAX Needle Sensor - 16G recall: There was an error in inspection and programming of the eTRAX needle sensor
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip…
-
Class II · 7 months ago
Intuitive Surgical, Inc. Brand Name: da Vinci S, Si Monopolar Curved Scissors recall: Due to increased complaints for broken/frayed grip cables for reusable
Due to increased complaints for broken/frayed grip cables for reusable instruments.
-
Class II · 7 months ago
Mentor Texas, LP. Artoura Breast Tissue Expanders Reference Numbers: SDC-100UH recall: Infusion sets may contain dull/blunt needle tip
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
-
Class II · 7 months ago
Burlington Medical, Blockers recall: Potential for attenuation degradation over time, decreasing the lifespan
Potential for attenuation degradation over time, decreasing the lifespan.
-
Class I · 7 months ago
Philips Respironics Trilogy Evo Universal recall: In some situations, the Obstruction Alarm does not trigger within
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
-
Class I · 7 months ago
Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00 recall: In some situations, the Obstruction Alarm does not trigger within
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
-
Class II · 7 months ago
Mentor Texas, LP. CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers recall: Infusion sets may contain dull/blunt needle tip
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
-
Class II · 7 months ago
Medtronic MiniMed, Inc. MiniMed 630G Insulin Pump recall: All Medtronic MiniMed infusion pumps (Paradigm series, 600 series
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and…
-
Class II · 7 months ago
RefleXion X1 Radiotherapy System Model RXM1000, Part #800-00006-00 recall: Due to a radiotherapy medical system software defect
Due to a radiotherapy medical system software defect, when performing angular roll corrections followed by a repeat localization, the roll…
-
Class II · 7 months ago
Philips Medical Systems Nederland B.v. Azurion 7 M12 recall: Philips has identified instances where X-ray imaging may not be initiated
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
-
Class II · 7 months ago
Medtronic MiniMed, Inc. MiniMed 640G Insulin Pump recall: All Medtronic MiniMed infusion pumps (Paradigm series, 600 series
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and…
-
Class II · 7 months ago
Medtronic MiniMed, Inc. MiniMed 780G Insulin Pump recall: All Medtronic MiniMed infusion pumps (Paradigm series, 600 series
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and…