Recalls affecting Florida
Notices that name Florida in their distribution area, plus every nationwide recall — nationwide recalls reach Florida too.
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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 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…
-
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…
-
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…
-
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…
-
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
Tornier HRS Max parts: 1. Tornier HRS Max Tuberosity Body Lat Coat recall: Affected products were incorrectly labeled as Tornier HRS Max products
Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are…
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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…
-
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
Stryker Sustainability Solution Color Cuff 24" Quick Connect Dual Port recall: Due to potential for tourniquet cuffs to detach from the bladder
Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.
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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…
-
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…
-
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…
-
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…
-
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…
-
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