Recalls affecting Kentucky
Notices that name Kentucky in their distribution area, plus every nationwide recall — nationwide recalls reach Kentucky too.
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Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/20 OR Table recall: The BIOS battery may deplete faster than initially anticipated during
The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the…
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Class I · 1+ years ago
Siemens Medical Solutions USA, Inc Magnetom Lumina recall: There is a potential for an ice blockage to form or currently exist within
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be…
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Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/10 recall: The BIOS battery may deplete faster than initially anticipated during
The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the…
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Class I · 1+ years ago
Siemens Medical Solutions USA, Inc Magnetom Verio recall: There is a potential for an ice blockage to form or currently exist within
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be…
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Class II · 1+ years ago
Schiller, Ag Argus PB-3000, Reference Numbers: 1A.701307 recall: Vital sign monitoring instrument may trigger an error message during blood
Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure…
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Class II · 1+ years ago
Getinge 88-Series Washer- Disinfector recall: Potential for device to overheat during operation if the circulation pressure
Potential for device to overheat during operation if the circulation pressure calibration was not performed or had been performed incorrectly, and…
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Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/15 recall: The BIOS battery may deplete faster than initially anticipated during
The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the…
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Class II · 1+ years ago
Northeast Scientific Inc. NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy recall: Potential for breaches in the sterile barrier packaging
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
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Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD10 recall: The BIOS battery may deplete faster than initially anticipated during
The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the…
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Class I · 1+ years ago
Medline Industries, LP Reprocessed Livewire Steerable Electrophysiology Catheter Item recall: Specific lots of reprocessed electrophysiology and ultrasound catheters
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual…
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Class I · 1+ years ago
Draeger, Inc. Brand Name: Atlan Product Name: Atlan A350 Model/ recall: The device either indicated a failure of the piston ventilator before use
The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
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Class II · 1+ years ago
ZAP-X recall: If the radiosurgery system triggers a proximity error message during a long
If the radiosurgery system triggers a proximity error message during a long gantry move (greater-than180 degrees), and a subsequent proximity error…
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Class II · 1+ years ago
MedicalCommunications GmbH Ashvins variant Heyex 2 / Heyex Pacs. Software Version recall: Potential that the measured value may be smaller than the actual area
Potential that the measured value may be smaller than the actual area.
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Class II · 1+ years ago
Northeast Scientific Inc. NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy recall: Potential for breaches in the sterile barrier packaging
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
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Class II · 1+ years ago
Northeast Scientific Inc. NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy recall: Potential for breaches in the sterile barrier packaging
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
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Class II · 1+ years ago
North American Rescue LLC. Junctional Emergency Treatment Tool , REF: 30-0088 recall: Device used for unilateral or bilateral occlusion of blood flow to the lower
Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the…
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Class I · 1+ years ago
Siemens Medical Solutions USA, Inc Biograph mMR recall: There is a potential for an ice blockage to form or currently exist within
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be…
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Class I · 1+ years ago
Siemens Medical Solutions USA, Inc Magnetom Skyra recall: There is a potential for an ice blockage to form or currently exist within
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be…
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Class II · 1+ years ago
Amerisource Health Services LLC Carbamazepine Extended-Release Tablets, USP 400 mg recall: Failed Dissolution Specifications
Failed Dissolution Specifications.
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Class II · 1+ years ago
Apotex Corp. Ketorolac Tromethamine Ophthalmic Solution, 0.5%, 5 mL recall: Lack of Assurance of Sterility; atypical weight loss due to improper bottle
Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns
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Class II · 1+ years ago
Zydus Pharmaceuticals Inc Entecavir Tablets, USP, 1 mg, 30-count bottle recall: Failed impurity/degradation specifications:Out of Specification result
Failed impurity/degradation specifications:Out of Specification result for an individual organic impurity
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Class II · 1+ years ago
Apotex Corp. Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution, 0.2%/0.5% recall: Lack of Assurance of Sterility; atypical weight loss due to improper bottle
Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns
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Class II · 1+ years ago
Zydus Pharmaceuticals Inc Entecavir Tablets, USP, 0.5 mg, 30-count bottle recall: Failed impurity/degradation specifications:Out of Specification result
Failed impurity/degradation specifications:Out of Specification result for an individual organic impurity
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Class II · 1+ years ago
Lawrence Wholesale LLC Shrimp Cocktail Bowl recall: Product manufactured under insanitary conditions whereby it may have
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)