Recalls affecting Nevada
Notices that name Nevada in their distribution area, plus every nationwide recall — nationwide recalls reach Nevada too.
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Class II · 4 months ago
Bard Access Systems, Inc. CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Boston Scientific Corporation CRE Wireguided 6-8mm 240cm recall: Potential sterile breach of the pouches in which devices are packaged
Potential sterile breach of the pouches in which devices are packaged.
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Class II · 4 months ago
Bard Access Systems, Inc. 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class I · 4 months ago
Baxter Healthcare Corporation Hillrom Volara System P.circuit 5KIT AC, , Model/ recall: There have been reports of air and medication leakage from the nebulizer cup
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead…
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Class I · 4 months ago
Windstone Medical Packaging, Inc. A M S, Aligned Medical Solutions recall: Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis)…
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Class II · 4 months ago
Bard Access Systems, Inc. OTP5000 Thora/Para Tray, 5FR recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Siemens Medical Solutions USA, Inc ARTIS icono floor recall: Potential for loss of movement capability after adjusting the detector lift
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
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Class II · 4 months ago
Zimmer Surgical Inc Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS recall: Potential sterility breach in sealing area of sterile pouch. If used
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use…
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Class I · 4 months ago
Windstone Medical Packaging, Inc. A M S, Aligned Medical Solutions, Dr. Lewin Pack recall: Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis)…
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Class II · 4 months ago
Medline Convenience Kits: 1) Block Tray recall: The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd…
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Class II · 4 months ago
Boston Scientific Corporation CRE Wireguided 15-18mm 240cm recall: Potential sterile breach of the pouches in which devices are packaged
Potential sterile breach of the pouches in which devices are packaged.
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Class II · 4 months ago
Boston Scientific Corporation CRE Wireguided 12-15mm 240cm recall: Potential sterile breach of the pouches in which devices are packaged
Potential sterile breach of the pouches in which devices are packaged.
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Class II · 4 months ago
Medline Convenience Kits: 1) Lumbar Puncture Choice recall: The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd…
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Class I · 4 months ago
Insulet Corporation Omnipod DASH Pod. Includes the below Model/REF Numbers: 1 recall: External soft cannula damage during manufacturing that results in insulin
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of…
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Class II · 4 months ago
Baxter Healthcare Corporation Adapter for Head Positioning, Model/ recall: The Adapter for Head Positioning accessory may become loose during patient
The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the…
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Class II · 4 months ago
Medline Convenience kits containing recalled Swan-Ganz Catheters Cabg recall: Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue)…
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Class II · 4 months ago
Accuray Incorporated Cyberknife Treatment Deliver System equipped with the Xchange recall: In certain cases, a collimator may not fully dock
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then…
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Class II · 4 months ago
Bard Access Systems, Inc. CK000662 PowerPicc Solo HF Catheter 5 Fr Triple-Lumen recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Boston Scientific Corporation CRE Wireguided 8-10mm 240cm recall: Potential sterile breach of the pouches in which devices are packaged
Potential sterile breach of the pouches in which devices are packaged.
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Class I · 4 months ago
Hamilton Medical AG Breathing circuit set, coaxial: REF: 260127, 260128, 260167 recall: Ventilator coaxial breathing circuit may have
Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test…
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Class II · 4 months ago
Medline Convenience Kits: 1) Arterial Access Tray W/Lidocaine recall: The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd…
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Class II · 4 months ago
Boston Scientific Corporation CRE Pro Wireguided 6-8mm 240cm recall: Potential sterile breach of the pouches in which devices are packaged
Potential sterile breach of the pouches in which devices are packaged.
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Class II · 4 months ago
W L Gore & Associates, Inc. Gore¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch recall: Due to catheter separation
Due to catheter separation
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Class II · 4 months ago
Covidien Shiley Disposable Decannulation Plug REF Ddcp Udi-Di code recall: Due to product labeling incorrectly including the symbol indicating non-DEHP
Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.