Recalls affecting New Mexico
Notices that name New Mexico in their distribution area, plus every nationwide recall — nationwide recalls reach New Mexico too.
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Class II · 4 months ago
Laborie Medical Technologies Corp Solar GI System recall: Under extended clinical use conditions (e.g
Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the…
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Class I · 4 months ago
Medline Industries, LP Reprocessed Electrophysiology Catheters and Ultrasound recall: Expansion of RES 98277. Specific lots of reprocessed catheters may contain
Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual…
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Class II · 4 months ago
Medline Convenience Kits: 1) Mercy Medical Circumcision 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
Medline Convenience Kits: 1) Arterial Line KIT 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
Siemens Medical Solutions USA, Inc ARTIS icono biplane 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 I · 4 months ago
Medtronic Harmony Delivery Catheter System recall: Devices containing inner shaft assemblies from specific manufacturing lots
Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the…
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Class II · 4 months ago
Bard Access Systems, Inc. 4380 Economy Soft Tissue Biopsy Tray 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 Pro 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 II · 4 months ago
Masimo Corporation Radius VSM Disposable NIBP Cuff, REF: 4825, 4826 recall: Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger…
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Class II · 4 months ago
Medline Convenience Kits: 1) Ophthalmic Pack W/Lido 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
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
Medline Convenience kits containing recalled Swan-Ganz Catheters CV 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 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
Boston Scientific Corporation CRE Wireguided 18-20mm 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. 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…