VehicleJul 14, 2026
Explorer body recall — NHTSA campaign 26V448000
Ford Motor Company (Ford) is recalling certain 2016-2019 Explorer vehicles. The roof rail covers may come loose and detach from the vehicle.
bodyFord Motor Company
July 2026 recalls — page 8
These records include useful source details for the selected month.
Medical DeviceJul 8, 2026
Baxter Healthcare Hillrom VOLARA P.CIRCUIT 5KIT recall — FDA Z-2549-2026
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 8, 2026
Medline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY recall — FDA Z-2545-2026
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. for Lidocaine Ampules due to quality…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 8, 2026
Medline Convenience Kits: 1) MULTIMED, 7FR, 20CM, 3L, CVC BUNDLE recall — FDA Z-2536-2026
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. for Lidocaine Ampules due to quality…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 8, 2026
Baxter Healthcare Hillrom VOLARA System P.CIRCUIT KIT recall — FDA Z-2548-2026
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 8, 2026
Bard Access Systems 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr recall — FDA Z-2660-2026
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Class IIFDA: OngoingBard Access Systems, Inc.
Medical DeviceJul 8, 2026
Insulet Omnipod (Eros) Pod recall — FDA Z-2605-2026
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The primary…
Class IFDA: OngoingInsulet Corporation
Medical DeviceJul 8, 2026
Hamilton Medical AG IntelliCuff, Portable automatic cuff pressure controller REF: 951001 recall — FDA Z-2625-2026
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 maintain the cuff pressure set by the user.
Class IIFDA: OngoingHamilton Medical AG
Medical DeviceJul 8, 2026
Medacta Usa Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971 recall — FDA Z-2618-2026
Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem reamer are positioned…
Class IIFDA: OngoingMedacta Usa Inc
Medical DeviceJul 8, 2026
Boston Scientific CRE Pro Wireguided 18-20mm 240cm recall — FDA Z-2631-2026
Potential sterile breach of the pouches in which devices are packaged.
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceJul 8, 2026
Sterile Tourniquet Hoses A.T.S 4000 TS Tourniquet Systems Dual Hose with CPC Connectors recall — FDA Z-2673-2026
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant…
Class IIFDA: OngoingZimmer Surgical Inc
Medical DeviceJul 8, 2026
Windstone Medical Packaging A M S, ALIGNED MEDICAL SOLUTIONS, Preop Kit-NS, Pack Number recall — FDA Z-2621-2026
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose…
Class IFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceJul 8, 2026
Windstone Medical Packaging A M S, ALIGNED MEDICAL SOLUTIONS, DSAEK Pack-RX, Pack Number recall — FDA Z-2619-2026
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose…
Class IFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceJul 8, 2026
Bard Access Systems 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 recall — FDA Z-2666-2026
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Class IIFDA: OngoingBard Access Systems, Inc.
Medical DeviceJul 8, 2026
Boston Scientific CRE Wireguided 10-12mm 240cm recall — FDA Z-2634-2026
Potential sterile breach of the pouches in which devices are packaged.
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceJul 8, 2026
Laborie Medical Technologies Solar GI System (Water Perfusion) recall — FDA Z-2669-2026
Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the…
Class IIFDA: OngoingLaborie Medical Technologies Corp
Medical DeviceJul 8, 2026
Medline Industries Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. recall — FDA Z-2615-2026
Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surfaces are…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceJul 8, 2026
Medline Convenience Kits: 1) MERCY MEDICAL CIRCUMCISION TRAY recall — FDA Z-2546-2026
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. for Lidocaine Ampules due to quality…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 8, 2026
Medline Convenience Kits: 1) ARTERIAL LINE KIT recall — FDA Z-2543-2026
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. for Lidocaine Ampules due to quality…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 8, 2026
Medtronic Harmony Delivery Catheter System recall — FDA Z-2624-2026
Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system under certain procedural or…
Class IFDA: OngoingMedtronic Heart Valves Division
Medical DeviceJul 8, 2026
Bard Access Systems 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A recall — FDA Z-2668-2026
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Class IIFDA: OngoingBard Access Systems, Inc.
Medical DeviceJul 8, 2026
Boston Scientific CRE Pro Wireguided 8-10mm 240cm recall — FDA Z-2627-2026
Potential sterile breach of the pouches in which devices are packaged.
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceJul 8, 2026
Masimo Radius VSM Disposable NIBP Cuff, REF: 4825, 4826 recall — FDA Z-2671-2026
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients,…
Class IIFDA: OngoingMasimo Corporation
Medical DeviceJul 8, 2026
Medline Convenience Kits: 1) OPHTHALMIC PACK W/LIDO recall — FDA Z-2547-2026
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. for Lidocaine Ampules due to quality…
Class IIFDA: OngoingMedline Industries, LP
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.