Recalls affecting South Dakota
Notices that name South Dakota in their distribution area, plus every nationwide recall — nationwide recalls reach South Dakota too.
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Class II · last month
Baxter Novum IQ Syringe Pump recall: A software issue that may occur during a Volume/Time (VOT) multi-syringe
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be…
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Class II · last month
Medline Convenience Kits: 1) LABOR CDS 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
Medline recall: Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an…
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Class II · last month
Medline Convenience Kits: 1) Ultrasound Breast Pack 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
Medline Convenience Kits: 1) DYKM1414 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
Fresenius Medical Care Renal Therapies Group, LLC Granuflo Dry Acid Concentrate recall: Complaints of blue-green discoloration in product
Complaints of blue-green discoloration in product
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Class II · last month
Medos International Sarl Velys Enabling Tech Robotic-Assist Station REF: 451611001 recall: Software issue within robotic controller which may cause unintended movement
Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning.
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Class II · last month
Fresenius Medical Care Renal Therapies Group, LLC 5008X Standard HD Pre-Flush 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
Medline recall: Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an…
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Class II · last month
AVID Medical, Inc. Halyard medical convenience kits labeled as: 1) ENT, Model/ 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
Boston Scientific Corporation Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac recall: There is potential for a delay in AF Burden Alert notification affecting
There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs)…
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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