Recalls affecting Ohio
Notices that name Ohio in their distribution area, plus every nationwide recall — nationwide recalls reach Ohio too.
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Class II · 7 months ago
Molded Products Inc See Luer Cap Set, MPC-130, set, administration, intravascular recall: Molded Products, Inc. is voluntarily conducting a medical device recall
Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline Industries, LP Namic Angiographic Syringe, labeled as follows: 1 recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class II · 7 months ago
Siemens Medical Solutions USA, Inc Artis pheno and Artis Icono biplane recall: During patient examinations, the system may sporadically display a major
During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient. Despite the reported dose…
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Class II · 7 months ago
Brahms GmbH B¿R¿A¿H¿M¿S Kryptor compact React, REF: 89986 recall: Customers have observed quality control values out of range at the lowest
Customers have observed quality control values out of range at the lowest quality control level (QC Level 1) for the PIGF assay which require…
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Class I · 7 months ago
Medline Industries, LP Namic Angiographic Syringe, labeled as follows: 1 recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline Industries, LP Namic Angiographic Control Syringe, labeled as follows: 1 recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class II · 7 months ago
Cipla USA, Inc. Lanreotide Injection, 120 mg*/0.5 mL recall: Lack of Assurance of Sterility: Due to an FDA observation at the contract
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
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Class II · 7 months ago
Fresenius Kabi USA, LLC 0.9% Sodium Chloride Injection, USP 900 mg per 100 mL , 1 recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
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Class II · 7 months ago
Teva Pharmaceuticals USA, Inc Isotretinoin Capsules, USP, 30 mg recall: Superpotent and Subpotent
Superpotent and Subpotent
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Class II · 7 months ago
GE Healthcare Ireland Limited GE Healthcare Omnipaque Injection, 300 mg/mL recall: Presence of particulate matter
Presence of particulate matter
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Class II · 7 months ago
Fagron Compounding Services Vancomycin HCL, 1 gram added to 250 mL recall: Lack of Assurance of Sterility; blue Break-Off-Part could detach
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
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Class II · 7 months ago
Teva Pharmaceuticals USA, Inc Isotretinoin Capsules, USP, 40 mg recall: Superpotent and Subpotent
Superpotent and Subpotent
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Class II · 7 months ago
Fresenius Kabi USA, LLC 0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL 250 mL recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
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Class II · 7 months ago
Fresenius Kabi USA, LLC 0.9% Sodium Chloride Injection, USP, 50 mL x60, Becton recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
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Class II · 7 months ago
Fresenius Kabi USA, LLC 0.9% Sodium Chloride Injection, USP 0.9% 50 mL recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
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Class II · 7 months ago
Fagron Compounding Services norepinephrine Bitartrate recall: Lack of Assurance of Sterility; blue Break-Off-Part could detach
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
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Class II · 7 months ago
Preferred Pharmaceuticals, Inc. Artificial Tears Lubricant Eye Drops recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
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Class II · 7 months ago
Viatris, Inc. Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles recall: Failed Dissolution Specifications
Failed Dissolution Specifications