Recalls published in July 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in July 2026, newest first.
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Class I · 4 months ago
Baxter Healthcare Corporation Hillrom Volara System P.circuit KIT , 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
Siemens Medical Solutions USA, Inc ARTIS icono ceiling 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
Bard Access Systems, Inc. 5605150 Power-Trialysis Short-Term Straight Dialysis 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
Insulet Corporation Omnipod Pod. Includes the below Model/REF Numbers: 1. POD-ZXP425 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
Hamilton Medical AG IntelliCuff, Portable automatic cuff pressure controller REF recall: Due to reported complaints, the cuff device may alarm with a "Cuff System
Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to…
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Class II · 4 months ago
Bd Switzerland Sarl Medline 111 Gravity SET W/3 Needle Free Y-Sites REF Dyndtn0555 recall: Due to engineering sample labeled "Not for Human Use" being inadvertently
Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market.
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Class II · 4 months ago
Medacta Usa Inc Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970 recall: Surgical instruments used during shoulder arthroplasty procedures does
Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming…
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Class II · 4 months ago
Boston Scientific Corporation CRE Pro 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
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, Preop Kit-NS 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 I · 4 months ago
Windstone Medical Packaging, Inc. A M S, Aligned Medical Solutions, Dsaek Pack-RX 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. 1174108 PowerPicc Catheter 4 Fr Single-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 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
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…