Recalls published in April 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in April 2026, newest first.
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Class II · 6 months ago
Cook Incorporated Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set recall: Products from the affected device lots were labeled with expiration dates
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
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Class I · 6 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 · 6 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 · 6 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 · 6 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 II · 6 months ago
Cook Medical Arterial Pressure Monitoring Tray, Reference recall: Products from the affected device lots were labeled with expiration dates
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
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Class I · 6 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 · 6 months ago
Xtant Medical Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm recall: Units from one lot were mislabeled with an incorrect part number
Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.
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Class II · 6 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 · 6 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 · 6 months ago
Teva Pharmaceuticals USA, Inc Isotretinoin Capsules, USP, 30 mg recall: Superpotent and Subpotent
Superpotent and Subpotent
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Class II · 6 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 · 6 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 · 6 months ago
Teva Pharmaceuticals USA, Inc Isotretinoin Capsules, USP, 40 mg recall: Superpotent and Subpotent
Superpotent and Subpotent
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Class II · 6 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 · 6 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 · 6 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 · 6 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 · 6 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 · 6 months ago
Viatris, Inc. Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles recall: Failed Dissolution Specifications
Failed Dissolution Specifications
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Class II · 6 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 · 6 months ago
Fresenius Kabi USA, LLC 5% Dextrose Injection, USP 5 g per 100 mL 100 mL in a 100 mL recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
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Class II · 6 months ago
Fresenius Kabi USA, LLC 5% Dextrose Injection, USP 12.5 g per 250 mL 250 mL in a 250 recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
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Class II · 6 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