Recalls affecting Oklahoma
Notices that name Oklahoma in their distribution area, plus every nationwide recall — nationwide recalls reach Oklahoma too.
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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…
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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.
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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…
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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…
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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
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
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 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.