Recalls published in April 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in April 2026, newest first.
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Azurion 3 M15 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.
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Class II · 7 months ago
Burlington Medical, Frontal Aprons recall: Potential for attenuation degradation over time, decreasing the lifespan
Potential for attenuation degradation over time, decreasing the lifespan.
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Class II · 7 months ago
Medtronic MiniMed, Inc. MiniMed 530G 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…
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Class II · 7 months ago
Ultradent Products, Inc. Jiffy Original recall: Composite polisher cups may crumble and break apart easily
Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.
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Class II · 7 months ago
Medline kits containing Olympus biopsy valves: 1. Bronch Procedure KIT 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…
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Class II · 7 months ago
ReCor Medical Inc. Brand Name: Paradise¿ Ultrasound Renal Denervation System Product recall: Due to firm distributing a nonconforming product that supposed to be scrapped
Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
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Class II · 7 months ago
Civco Medical Instruments Co. Inc. eTRAX Needle Sensor - 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…
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD20 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.
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Class II · 7 months ago
Enfit G-Tube Connector, Medline recall: Connectors were not manufactured to required dimensional specifications
Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to…
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Class II · 7 months ago
Intuitive Surgical, Inc. Brand Name: da Vinci S, Si Grasping Retractor Instrument recall: Due to increased complaints for broken/frayed grip cables for reusable
Due to increased complaints for broken/frayed grip cables for reusable instruments.
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Class II · 7 months ago
Burlington Medical, Protective Sleeves recall: Potential for attenuation degradation over time, decreasing the lifespan
Potential for attenuation degradation over time, decreasing the lifespan.
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Class II · 7 months ago
Mentor Texas, LP. Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H 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.
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/10 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.
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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.
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Class II · 7 months ago
Medline kits containing Olympus biopsy valves: 1. Bronchoscopy 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…
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Class I · 7 months ago
Abiomed, Inc. Purge Cassette, sold within Impella Pump Sets and Individually recall: Increased risk of purge leaks with Generation 1 purge cassettes
Increased risk of purge leaks with Generation 1 purge cassettes.
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Class II · 7 months ago
Burlington Medical, Kilt Blockers recall: Potential for attenuation degradation over time, decreasing the lifespan
Potential for attenuation degradation over time, decreasing the lifespan.
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Class II · 7 months ago
Medline Kits containing Enfit G-Tube Connector 1. SKU Dykm2720 G/J Tube recall: Connectors were not manufactured to required dimensional specifications
Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to…
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Class II · 7 months ago
Medtronic MiniMed, Inc. Paradigm REAL-Time Revel 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…
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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.
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Class II · 7 months ago
Siemens Healthcare Diagnostics, Inc. Atellica CH Enzymatic Hemoglobin A1c recall: A potential for depressed results for Atellica CH A1c_E when processing
A potential for depressed results for Atellica CH A1c_E when processing Atellica CH RCRP on the same analyzer. Customers processing A1c_E and RCRP on…
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD10F 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.
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Class II · 7 months ago
Burlington Medical, Demi Half Aprons recall: Potential for attenuation degradation over time, decreasing the lifespan
Potential for attenuation degradation over time, decreasing the lifespan.
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Class II · 7 months ago
Brand Name: Olympus Soltive Premium SuperPulsed Laser System Product 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…