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 · 5 months ago
Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers recall: Affected devices exhibited fractures at the distal shaft tip without complete
Affected devices exhibited fractures at the distal shaft tip without complete detachment.
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Class II · 5 months ago
C.R. Bard Inc Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 recall: Due to stain present on the surface of affected foley catheters
Due to stain present on the surface of affected foley catheters.
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Class II · 5 months ago
Novapproach Spine, LLC OneLIF Interbody Cage : 010-107-1007/Small 7 Degree 10mm X 7mm recall: Intervertebral body fusion system straight inserter failed to properly attach
Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage…
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Class II · 5 months ago
Philips Azurion systems not configured with an optional auxiliary pan recall: Potential safety issue with Philips Azurion systems
Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the…
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Class II · 5 months ago
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Becton, Dickinson and Company Swan-Ganz Pacing Catheter, Models: D200F7 recall: Catheters may, due to a manufacturing process and material changes
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to…
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Class II · 5 months ago
Medtronic Gundry Retrograde Cannula Manual-Inflate Silicone Body 13FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall: Certain lots of product have the potential for a sterile barrier breach
Certain lots of product have the potential for a sterile barrier breach.
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Class II · 5 months ago
Philips Medical Systems Nederland B.v. Azurion system recall: The deaeration hose in X-ray tube cooling units type CU3101
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially…
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Class II · 5 months ago
Becton, Dickinson and Company Swan-Ganz Jr Catheter, Models: Sgpt54, Sgpt64P, Sgpt755P recall: Catheters may, due to a manufacturing process and material changes
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to…
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Class II · 5 months ago
Haleon US Holdings LLC Gas-X, Simethicone 125 mg/ Antigas, 120 SoftGels recall: Labeling: Not Elsewhere Classified- Incomplete inactive ingredient
Labeling: Not Elsewhere Classified- Incomplete inactive ingredient information on the carton labeling.
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Class III · 5 months ago
Lannett Company Inc. Primidone Tablets USP, 250mg, 100-count bottle recall: Cross contamination with other products: API contaminated with trace amounts
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
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Class III · 5 months ago
Sagent Pharmaceuticals Busulfan Injection, 60 mg per 10 mL , 8x10 mL Single-Dose Vials recall: Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
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Class II · 5 months ago
ANI Pharmaceuticals, Inc. Estradiol Gel, 0.1%, 0.25 mg, 0.25 g per packet recall: Defective Container; packets were found to be either empty or partially full
Defective Container; packets were found to be either empty or partially full.
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Class III · 5 months ago
Amerisource Health Services LLC Primidone Tablets, USP, 250 mg, 100 Tablets per carton recall: Cross contamination with other products: API contaminated with trace amounts
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
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Class II · 5 months ago
UCB Biosciences Inc. cimzia , 2x200mg/mL Prefilled Syringes recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
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Class III · 5 months ago
Golden State Medical Supply Inc. Primidone Tablets, USP, 250 mg, 100-count bottle recall: Cross contamination with other products: API contaminated with trace amounts
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
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Class III · 5 months ago
Golden State Medical Supply Inc. Primidone Tablets, USP, 50 mg, 50-count bottle recall: Cross contamination with other products: API contaminated with trace amounts
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
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Class III · 5 months ago
Amerisource Health Services LLC Primidone Tablets, USP, 50 mg, 100 Tablets per carton recall: Cross contamination with other products: API contaminated with trace amounts
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
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Class II · 5 months ago
Zydus Pharmaceuticals Inc Erythromycin Tablets, USP, 250 mg, 30 tablets per bottle recall: CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
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Class II · 5 months ago
Lupin Pharmaceuticals Inc. Liraglutide Injection, 18 mg/3 mL recall: Presence of particulate matter: a white thread-like structure in the cartridge
Presence of particulate matter: a white thread-like structure in the cartridge