Recalls published in November 2025
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in November 2025, newest first.
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Class II · 11 months ago
Medline convenience kits labeled as: 1) Central Line Pack recall: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker…
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Class II · 11 months ago
Anatomy Supply Partners, LLC. Safe-T-Fill Plastic Blood Gas Capillary Tubes, 230 ¿L recall: Due to products manufactured under an inadequate quality system to include
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
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Class II · 11 months ago
Medline convenience kits labeled as: 1) Minor EYE Tray #81 recall: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker…
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Class II · 11 months ago
Cellavision AB REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer recall: Automated cell-locating device barcode reader may read the barcode
Automated cell-locating device barcode reader may read the barcode of the previously processed slide resulting in a misattribution of diagnostic…
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Class II · 11 months ago
Anatomy Supply Partners, LLC. Safe-T-Fill Micro Capillary Blood Collection, 200 ¿L recall: Due to products manufactured under an inadequate quality system to include
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
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Class II · 11 months ago
Medline convenience kits labeled as: Circumcision Pack, REF Dynj16826O recall: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker…
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Class II · 11 months ago
Anatomy Supply Partners, LLC. Safe-T-Fill MicroHematocrit Capillary Tubes, 50 ¿L recall: Due to products manufactured under an inadequate quality system to include
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
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Class II · 11 months ago
Anatomy Supply Partners, LLC. Safe-T-Fill Micro Capillary Blood Collection, 125 ¿L recall: Due to products manufactured under an inadequate quality system to include
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
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Class II · 11 months ago
Anatomy Supply Partners, LLC. Safe-T-Fill Micro Capillary Blood Collection, 200 ¿L recall: Due to products manufactured under an inadequate quality system to include
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
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Class II · 11 months ago
Anatomy Supply Partners, LLC. Safe-T-Fill End Caps for Safe-T-Fill Blood Gas recall: Due to products manufactured under an inadequate quality system to include
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
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Class II · 11 months ago
Medline convenience kits labeled as: 1) ACH Plastics Breast-Lf recall: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker…
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Class II · 11 months ago
DermaRite Industries, LLC DermaCerin, Skin Protectant Moisturizing Cream recall: CGMP Deviation; manufactured at the same facility where other products
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
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Class III · 11 months ago
Alembic Pharmaceuticals Limited Fesoterodine Fumarate, Extended-release Tablets recall: Failed Impurities/Degradation Specifications: Due to levels of 'Diester
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
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Class II · 11 months ago
DermaRite Industries, LLC 4-N-1 Skin Protectant, No Rinse Wash Cream with Dimethicone recall: CGMP Deviation; manufactured at the same facility where other products
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
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Class III · 11 months ago
Imprimis NJOF, LLC Klarity-C Drops 0.1%, Preservative-Free Sterile Ophthalmic Emulsion recall: Subpotent Drug
Subpotent Drug
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Class II · 11 months ago
DermaRite Industries, LLC McKesson Skin Protectant, Lanolin USP recall: CGMP Deviation; manufactured at the same facility where other products
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
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Class II · 11 months ago
Zydus Pharmaceuticals Inc Bromocriptine Mesylate Capsules, USP, 5 mg recall: Failed Impurities/Degradation Specifications: Out of Specification (OOS)
Failed Impurities/Degradation Specifications: Out of Specification (OOS) result reported for 2- Bromoergine impurity of Bromocriptine Mesylate…
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Class II · 11 months ago
DermaRite Industries, LLC Lantiseptic, Dry Skin Therapy, Lanolin USP 30% recall: CGMP Deviation; manufactured at the same facility where other products
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
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Class II · 11 months ago
DermaRite Industries, LLC Renew Skin Repair Cream, Dimethicone 1.5% recall: CGMP Deviation; manufactured at the same facility where other products
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
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Class II · 11 months ago
Park Avenue Compounding Fentanyl citrate, 2 mcg / ml / Ropivacaine recall: CGMP Deviations: Revised interpretation of Acceptable Quality Level (AQL)
CGMP Deviations: Revised interpretation of Acceptable Quality Level (AQL) results.
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Class I · 11 months ago
Otsuka ICU Medical LLC Potassium Chloride Inj., 20 mEq total in 50 mL Flexible recall: Labeling: Label Error on Declared Strength-The overwrap label may incorrectly
Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of…
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Class II · 11 months ago
DermaRite Industries, LLC Hand-E-Foam, Benzethonium Chloride 0.20% recall: CGMP Deviation; manufactured at the same facility where other products
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
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Class II · 11 months ago
DermaRite Industries, LLC GelRite Instant Hand Sanitizer, Alcohol 65% recall: CGMP Deviation; manufactured at the same facility where other products
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
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Class II · 11 months ago
DermaRite Industries, LLC UltraSure Anti-Perspirant & Deodorant recall: CGMP Deviation; manufactured at the same facility where other products
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.