Recalls published in September 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in September 2026, newest first.
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Class II · last month
Cardinal Health 200, LLC Presource Packs Containing CliniClean Pericare Wipes within recall: The Urinary Catheter Trays contain CliniClean Pericare Wipes
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing…
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Class II · last month
Johnson & Johnson Surgical Vision, Inc. Healon EndoCoat PRO recall: Surgical instructions sent for viscoelastic products used during ophthalmic
Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is…
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Class II · last month
Cardinal Health 200, LLC Presource Packs Containing CliniClean Pericare Wipes within recall: The Urinary Catheter Trays contain CliniClean Pericare Wipes
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing…
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Class II · last month
Fresenius Medical Care Renal Therapies Group, LLC 5008X HD/HDF with Twister Blood recall: Heightened probability of blood leak from the connection between the Arterial
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may…
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Class II · last month
Cardinal Health 200, LLC Presource Packs Containing CliniClean Pericare Wipes within recall: The Urinary Catheter Trays contain CliniClean Pericare Wipes
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing…
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Class II · last month
Cardinal Health 200, LLC Presource Packs Containing CliniClean Pericare Wipes within recall: The Urinary Catheter Trays contain CliniClean Pericare Wipes
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing…
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Class II · last month
Diagnostica Stago, Inc. STA Staclot Protein S, Model/ recall: A positive drift in QC values within the reagent's stated 4-hour onboard
A positive drift in QC values within the reagent's stated 4-hour onboard stability period was identified
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Class II · last month
AVID Medical, Inc. Halyard medical convenience kits labeled as: 1) A-P PACK - 205936 recall: The recall notice was initiated due to a Medicom Urgent Medical Device
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges…
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Class II · last month
Medline Convenience Kits: 1) Blood Culture Tray Pediatric recall: The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to…
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Class II · last month
Golden State Medical Supply Inc. Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle recall: Failed Dissolution Specifications. Notification from the manufacturer
Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution
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Class II · last month
Mylan Pharmaceuticals Inc Carton label: Mycophenolate Mofetil for injection, USP recall: Failed Dissolution Specifications
Failed Dissolution Specifications
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Class II · last month
Baxter Healthcare Corporation Clindamycin Phosphate in 0.9% Sodium Chloride Injection recall: CGMP Deviations
CGMP Deviations
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Class II · last month
Baxter Healthcare Corporation Vancomycin Injection, USP in 5% Dextrose, 1 g per 200mL recall: CGMP Deviations
CGMP Deviations
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Class II · last month
Baxter Healthcare Corporation Clindamycin Injection USP in 5% Dextrose, 900 mg/50 mL recall: CGMP Deviations
CGMP Deviations
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Class II · last month
Mylan Pharmaceuticals Inc Prasugrel Tablets, USP, 10mg recall: Failed Dissolution Specifications; product failed to meet 18-month stability
Failed Dissolution Specifications; product failed to meet 18-month stability testing acceptance criteria
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Class III · last month
Chiesi USA, Inc. Revcovi Injection, 2.4mg/1.5mL , Single-Dose Vial recall: Failed Stability Specifications: Out of specification stability result
Failed Stability Specifications: Out of specification stability result for the protein concentration profile.
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Class II · last month
Sage Products, LLC 2% Chlorhexidine Gluconate* Cloth, Non-sterile recall: Cross Contamination with Other Products
Cross Contamination with Other Products
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Class II · last month
Baxter Healthcare Corporation Vasopressin, in 0.9% Sodium Chloride Injection recall: CGMP Deviations
CGMP Deviations
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Class II · last month
Baxter Healthcare Corporation Vancomycin Injection, USP, in 0.9% Sodium Chloride recall: CGMP Deviations
CGMP Deviations
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Class II · last month
Baxter Healthcare Corporation Famotidine Injection in Sodium Chloride Injection, 20 mg recall: CGMP Deviations
CGMP Deviations
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Class III · last month
Bionpharma Inc. Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 recall: Presence of Foreign Tablets/Capsules
Presence of Foreign Tablets/Capsules
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Class II · last month
Baxter Healthcare Corporation Myxredlin, Insulin Human in 0.9% Sodium Chloride recall: CGMP Deviations
CGMP Deviations
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Class II · last month
Lexia LLC Broadway Joe's Pain Cream, 3000 gm CBD, ,4 oz-jar recall: CGMP Deviations: Potential contamination of raw material
CGMP Deviations: Potential contamination of raw material
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Class II · last month
Baxter Healthcare Corporation Clindamycin Injection USP in 5% Dextrose, 900 mg/50 mL recall: CGMP Deviations
CGMP Deviations