Recalls affecting Louisiana
Notices that name Louisiana in their distribution area, plus every nationwide recall — nationwide recalls reach Louisiana too.
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Class II · 1+ years ago
Merit Medical Systems, Inc. 10Fore Hemostasis Valve recall: Due to a manufacturing issue involving the silicone quad ring where the ring
Due to a manufacturing issue involving the silicone quad ring where the ring is deformed or otherwise damaged and may cause a foreign body in the…
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Class II · 1+ years ago
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical recall: Retroactive; Due to complaints, labeling correction for permanent
Retroactive; Due to complaints, labeling correction for permanent tissue-integrating surgical matrices to include prevention and management of would…
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Class II · 1+ years ago
Encore Medical, LP Brand Name: DJO Surgical Product Name: Altivate Reverse Wedge recall: Their is a potential that the reamer may kick or bind up during
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
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Class II · 1+ years ago
Omnia Medical TiBrid Stand Alone Intervertebral Body Fusion Device recall: Failure of fusion system instruments in the field
Failure of fusion system instruments in the field.
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Class II · 1+ years ago
Boston Scientific Corporation Preventive Maintenance Kit Icefx recall: Certain desiccant tube subassemblies were built with end caps
Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.
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Class II · 1+ years ago
Encore Medical, LP Brand Name: DJO Surgical Product Name: FA S Altivate Reverse recall: Their is a potential that the reamer may kick or bind up during
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
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Class II · 1+ years ago
Seaspine Orthopedics Corporation Reef TA Inserter recall: Inserter, used as part of a system with an intervertebral body fusion device
Inserter, used as part of a system with an intervertebral body fusion device, may contribute to difficulty disengaging the implant or improper…
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Class II · 1+ years ago
AVID Medical, Inc. Halyard, ENT PACK recall: Potential for open header bag seals, compromising sterility
Potential for open header bag seals, compromising sterility.
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Class II · 1+ years ago
Orthofix U.S. LLC Pillar SA Ti, Sterile, 37mm x 28mm x 18mm , 20-degrees recall: A 37 mm implant width intervertebral body fusion device has a labeling
A 37 mm implant width intervertebral body fusion device has a labeling discrepancy with incorrect width of 33 mm stated on the outer label side flap…
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Class I · 1+ years ago
Olympus Corporation of the Americas ViziShot 2FLEX. Single Use Aspiration Needle recall: Potential for undetected, deformed a-traumatic tips
Potential for undetected, deformed a-traumatic tips.
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Class II · 1+ years ago
Quidel Corporation QuickVue recall: Dipstick strep A test has potential for false positive results
Dipstick strep A test has potential for false positive results.
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Class II · 1+ years ago
Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked recall: Measles IgM Test Kit lacks premarket approval or clearance
Measles IgM Test Kit lacks premarket approval or clearance.
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Class II · 1+ years ago
Philips Medical Systems Nederland B.V. IntelliSpace Cardiovascular, Software 8.0.0.4 recall: Software issue that results in the display of outdated information
Software issue that results in the display of outdated information.
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Class II · 1+ years ago
Siemens Medical Solutions USA, Inc Artis Pheno. Image-Intensified Flouroscopic X-Ray recall: Limited system movements after startup
Limited system movements after startup .
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Class II · 1+ years ago
Boston Scientific Corporation ICEfx Cryoablation System recall: Certain desiccant tube subassemblies were built with end caps
Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.
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Class II · 1+ years ago
Encore Medical, LP Brand Name: DJO Surgical Product Name: Altivate Reverse Wedge recall: Their is a potential that the reamer may kick or bind up during
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
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Class II · 1+ years ago
Major Pharmaceuticals and Rugby Laboratories Sulfamethoxazole and Trimethoprim recall: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil
Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC)…
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Class II · 1+ years ago
Zydus Pharmaceuticals Inc Chlorpromazine Hydrochloride Tablets, USP, 10 mg recall: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
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Class II · 1+ years ago
Major Pharmaceuticals and Rugby Laboratories Sulfamethoxazole and Trimethoprim recall: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil
Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC)…
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Class II · 1+ years ago
Exela Pharma Sciences LLC 4.2% Sodium Bicarbonate Injection, USP, 5 mEq/10 mL recall: Failed Impurities/Degradation Specifications: out of specification results
Failed Impurities/Degradation Specifications: out of specification results for arsenic in the impurities tested.
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Class II · 1+ years ago
Zydus Pharmaceuticals Inc Chlorpromazine Hydrochloride Tablets, USP recall: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
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Class II · 1+ years ago
Grace & Fire Pty Ltd Ultra Violette, Velvet Screen SPF 50, Blurring Mineral Skinscreen recall: Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed
Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and…
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Class II · 1+ years ago
Zydus Pharmaceuticals Inc Chlorpromazine Hydrochloride Tablets, USP recall: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
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Class II · 1+ years ago
Zydus Pharmaceuticals Inc Succinylcholine Chloride Injection, USP 200 mg/10 mL recall: Failed Impurities/Degradation Specifications: Out-of-Specification test
Failed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation impurity.