Recalls affecting Texas
Notices that name Texas in their distribution area, plus every nationwide recall — nationwide recalls reach Texas too.
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Class II · 7 months ago
Medtronic MiniMed, Inc. MiniMed 670G 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 B12 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
Synthes Products LLC 2.4 Volt TAP Cortex Screw TO 90MM recall: A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9
A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps…
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD10C 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
Medline Anterior HIP Pack Dynj64672B 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
Medtronic MiniMed, Inc. MiniMed 700G 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
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. Vue Motion V12. Product Number: 1017979 recall: Potential that mis-ordered frames in Vue Motion during dynamic cine runs
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Azurion 7 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.
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD20 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, BAT Coverage 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
Intuitive Surgical, Inc. Brand Name: da Vinci S, Si Tenaculum Forceps Instrument recall: Due to increased in complaints regarding frayed or broken pitch cables
Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
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Class II · 7 months ago
Burlington Medical, Kilt 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
Philips Medical Systems Nederland B.v. Allura Xper FD20/20 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
Philips Medical Systems Nederland B.v. Allura Xper FD20/15 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 I · 7 months ago
Philips Respironics Trilogy Evo, 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.
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Class II · 7 months ago
Burlington Medical, Caps 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 Olympus biopsy valves: 1. BAL 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
Stryker Chromophare Softlit Ring recall: Surgical light assembly may not adequate support the weight of the ceiling
Surgical light assembly may not adequate support the weight of the ceiling cover.
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD10 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
Burlington Medical, Thyroid Shield 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
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.
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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…
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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.