Latest recalls — page 70
Older notices, newest first.
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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
Syringe Luer LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product recall: A single lot of expired syringes were distributed due to a distribution
A single lot of expired syringes were distributed due to a distribution system control failure.
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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.
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Class II · 4 months ago
Boston Scientific Corporation CRE Pro 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
Bard Access Systems, Inc. 1274108D PowerPicc SV Catheter 4 Fr Dual-Lumen Rekw2449 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
Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN recall: May contain incorrect connectors and will not attach or misconnect to ENFit
May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in…
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Class II · 4 months ago
Siemens Medical Solutions USA, Inc ARTIS icono ceiling recall: Potential issue with the Display ceiling suspension (DCS Fix XL) that holds
Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place. Over time some screws that keep the monitor…
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Class II · 4 months ago
Boston Scientific Corporation CRE Pro Wireguided 10-12mm 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
Raysearch Laboratories Ab RayCare 2024A SP4. Oncology Information Systems recall: Beam set delivery note issues in which there is potential data loss
Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is…
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Class II · 4 months ago
Medline Convenience Kits: 1) Pain Mgmt/ Pref W. MED NDL 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
Medline Convenience kits containing recalled Swan-Ganz Catheters Right 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
Medline Convenience Kits: 1) DYNJ0621189X 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
Baxter Healthcare Corporation Hillrom Volara System P.circuit KIT 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 II · 4 months ago
Bard Access Systems, Inc. CK000525B PowerPicc Provena Solo Catheter 4 Fr Dual-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
Bard Access Systems, Inc. 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 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
Bard Access Systems, Inc. CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI 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
Medline Convenience Kits: 1) Suturing SET 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
Medline Convenience Kits: 1) PI CVC KIT 3L 7 FR 16 CM 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…