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 I · 9 months ago
Boston Scientific Corporation HOT AXIOS Stent and Electrocautery-Enhanced Delivery recall: Increased reports of stent deployment and expansion issues. The most common
Increased reports of stent deployment and expansion issues. The most common outcome reasonably foreseeable resulting from difficulty deploying the…
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Class II · 9 months ago
Olympus Corporation of the Americas Product Name: Disposable Triple Lumen recall: Devices which did not undergo thermoforming could deform and lose performance
Devices which did not undergo thermoforming could deform and lose performance.
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Class II · 9 months ago
Fujirebio Diagnostics, Inc. Product Name: Lumipulse G pTau 217 Plasma Calibrators recall: Customers may experience inaccurate test results by observing a higher
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low…
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Class II · 9 months ago
Etac A/S Brand Name: Molift Product Name: Molift Mover 205 Model/ recall: A customer experienced that during assembly and load testing of the device
A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation…
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Class II · 9 months ago
Olympus Corporation of the Americas Product Name: Single Use 3-Lumen Sphincterotome V recall: Devices which did not undergo thermoforming could deform and lose performance
Devices which did not undergo thermoforming could deform and lose performance.
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Class II · 9 months ago
Olympus Corporation of the Americas Product Name: Disposable Triple Lumen recall: Devices which did not undergo thermoforming could deform and lose performance
Devices which did not undergo thermoforming could deform and lose performance.
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Class II · 9 months ago
Changchun Wancheng Bio-Electron Co., Ltd. Exploro Highly Sensitive Male Fertility / recall: Test strips and other tests including for near-patient testing
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S…
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Class II · 9 months ago
Biomerieux Inc VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B o recall: Potential risk of Quality Control failures and/or false resistant antibiotic
Potential risk of Quality Control failures and/or false resistant antibiotic results when testing isolates of Enterobacterales/Enterobacteriaceae…
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Class II · 9 months ago
Changchun Wancheng Bio-Electron Co., Ltd. Male Fertility Sperm Test for Home Use recall: Test strips and other tests including for near-patient testing
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S…
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Class II · 9 months ago
Olympus Corporation of the Americas Product Name: Single Use 3-Lumen Sphincterotome V recall: Devices which did not undergo thermoforming could deform and lose performance
Devices which did not undergo thermoforming could deform and lose performance.
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Class II · 9 months ago
Olympus Corporation of the Americas Product Name: Single Use 3-Lumen Sphincterotome V recall: Devices which did not undergo thermoforming could deform and lose performance
Devices which did not undergo thermoforming could deform and lose performance.
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Class II · 9 months ago
Etac A/S Brand Name: Molift Product Name: Molift 4-point sling bars Model/ recall: A customer experienced that during assembly and load testing of the device
A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation…
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Class II · 9 months ago
Fujirebio Diagnostics, Inc. Product Name: Lumipulse pTau 217 Plasma Controls Model/ recall: Customers may experience inaccurate test results by observing a higher
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low…
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Class II · 9 months ago
Olympus Corporation of the Americas Product Name: Disposable Triple Lumen recall: Devices which did not undergo thermoforming could deform and lose performance
Devices which did not undergo thermoforming could deform and lose performance.
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Class II · 9 months ago
Olympus Corporation of the Americas Product Name: Single Use 3-Lumen Sphincterotome V recall: Devices which did not undergo thermoforming could deform and lose performance
Devices which did not undergo thermoforming could deform and lose performance.
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Class II · 9 months ago
Beckman Coulter, Inc. Coulter DxH Diluent, REF 628017 Coulter DxH ECO Diluent REF recall: Due to specific lots of diluents contributing to elevated platelet Daily
Due to specific lots of diluents contributing to elevated platelet Daily Checks background counts cycle with use with analyzers.
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Class II · 9 months ago
Vortex Surgical Inc. Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2 recall: There may be voids located in the seal of Tyvek pouches associated
There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has…
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Class II · 9 months ago
Sun Pharmaceutical Industries Inc Diclofenac Sodium, Topical Gel, 3%, 100 g tube recall: Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower
Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower than the limit] result in viscosity for Diclofenac Sodium Gel, 3%.
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Class II · 9 months ago
Granules Pharmaceuticals Inc. Trazodone Hydrochloride, USP, 50 mg, 100-Count Bottle recall: Presence of Foreign Tablets/Capsules
Presence of Foreign Tablets/Capsules
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Class I · 9 months ago
Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10 recall: Marketed without an Approved NDA/ANDA: FDA analysis found this product
Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil
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Class II · 9 months ago
Unichem Pharmaceuticals USA Inc. Bisoprolol Fumarate and Hydrochlorothiazide tablets recall: cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity
cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
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Class III · 9 months ago
Fazt & Loud LLC Lost and Found Energy, Sour Gummy Bear, 12pck, 16oz Cans Case recall: Recall is due to a misprint on the label that incorrectly identifies
Recall is due to a misprint on the label that incorrectly identifies the total caffeine content on the can. The item contains 300mg of caffeine…
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Class III · 9 months ago
OptiWize Health OptiWize Collagen Plus 320 count bottle recall: The firm initiated a voluntary recall after NSF testing showed that labeled
The firm initiated a voluntary recall after NSF testing showed that labeled ingredient quantities did not align with analytical test results…
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Class II · 9 months ago
Beacon Promotions Inc Repackaged M&Ms Peanut candies recall: Undeclared allergens (milk, soy, and peanut)
Undeclared allergens (milk, soy, and peanut)