FoodJul 8, 2026
MARS SNACKING MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein recall — FDA H-1129-2026
Potential contamination with plastic material
Class IIFDA: OngoingMARS SNACKING
July 2026 recalls — page 13
These records include useful source details for the selected month.
VehicleJul 7, 2026
Subaru of labels recall — NHTSA campaign 26V436000
Subaru of America, Inc. (Subaru) is recalling certain 2026 Crosstrek Hybrid, 2025-2026 Forester Hybrid, Forester, and 2019-2026 Ascent vehicles. These vehicles were manufactured with an…
labelsSubaru of America, Inc.
VehicleJul 1, 2026
Ram 1500 headlights recall — NHTSA campaign 26V421000
Chrysler (FCA US, LLC) is recalling certain 2026 Ram 1500 vehicles. The headlight wiring may cause the parking lights and daytime running lights to flicker on and off, or fail. As such,…
headlightsChrysler (FCA US, LLC)
VehicleJul 1, 2026
Odyssey camera recall — NHTSA campaign 26V423000
Honda (American Honda Motor Co.) is recalling certain 2018-2020 Odyssey vehicles. Water may enter into the rearview camera, which can cause the rearview camera image to fail to display when…
cameraHonda (American Honda Motor Co.)
Medical DeviceJul 1, 2026
Philips Telemetry Monitor 5500 1.4 GHz recall — FDA Z-2579-2026
Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure to reconnect to the PIC iX…
Class IIFDA: OngoingPhilips North America Llc
Medical DeviceJul 1, 2026
Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw recall — FDA Z-2532-2026
Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use.
Class IIFDA: OngoingAcumed LLC
Medical DeviceJul 1, 2026
Medline Industries Convenience kits containing select SKUs of 10mL Polycarbonate Colored recall — FDA Z-2596-2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 1, 2026
Medline Industries Convenience kits containing select SKUs of 10mL Polycarbonate Colored recall — FDA Z-2583-2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 1, 2026
Medline Industries Convenience kits containing select SKUs of 10mL Polycarbonate Colored recall — FDA Z-2593-2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 1, 2026
Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low recall — FDA Z-2602-2026
Potential for thrombus formation during prolonged use of the introducer.
Class IFDA: OngoingAbiomed, Inc.
Medical DeviceJul 1, 2026
Medline Industries Convenience kits containing select SKUs of 10mL Polycarbonate Colored recall — FDA Z-2586-2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 1, 2026
Medline Industries Convenience kits containing select SKUs of 10mL Polycarbonate Colored recall — FDA Z-2589-2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 1, 2026
Medline Industries Convenience kits containing select SKUs of 10mL Polycarbonate Colored recall — FDA Z-2584-2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 1, 2026
Medline Convenience Kits: 1) OPEN HEART CDS recall — FDA Z-2453-2026
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceJul 1, 2026
TMJ Solutions TMJ Bilateral Implants, REF: CHG020 recall — FDA Z-2524-2026
Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.
Class IIFDA: OngoingTMJ Solutions Inc
Medical DeviceJul 1, 2026
Medline Convenience Kits: 1) DRAWER 6 CENTRAL LINE INSERTIO recall — FDA Z-2454-2026
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceJul 1, 2026
Philips Avalon Fetal Monitor, FM 30 Part numberM2703A recall — FDA Z-2523-2026
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker…
Class IIFDA: OngoingPhilips North America Llc
Medical DeviceJul 1, 2026
Medtronic Perfusion Systems Octopus Evolution Tissue Stabilizer, Model TS2000 recall — FDA Z-2575-2026
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister,…
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceJul 1, 2026
GE Medical Systems SCS GE Healthcare AW Server 3.2 ext.6.5 recall — FDA Z-2553-2026
GE HealthCare has become aware of a context synchronization issue in AW Server 3.2 ext. 6.5. When a user selects a patient or exam in the AW Server Web Client worklist and launches an…
Class IIFDA: OngoingGE Medical Systems SCS
Medical DeviceJul 1, 2026
Medline Industries Convenience kits containing select SKUs of 10mL Polycarbonate Colored recall — FDA Z-2595-2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 1, 2026
Medline Industries Convenience kits containing select SKUs of 10mL Polycarbonate Colored recall — FDA Z-2588-2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 1, 2026
Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE recall — FDA Z-2455-2026
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceJul 1, 2026
Medline Industries Convenience kits containing select SKUs of 10mL Polycarbonate Colored recall — FDA Z-2594-2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJul 1, 2026
Medline Industries Convenience kits containing select SKUs of 10mL Polycarbonate Colored recall — FDA Z-2581-2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
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.