FoodAug 12, 2026
Clover Hill Dairy Soft Ricotta recall — FDA H-1199-2026
Product contaminated with Listeria monocytogenes.
Class IFDA: OngoingClover Hill Dairy, LLC
August 2026 recalls — page 11
These records include useful source details for the selected month.
FoodAug 12, 2026
Clover Hill Dairy Pepper Jack Cheese recall — FDA H-1215-2026
Product contaminated with Listeria monocytogenes.
Class IFDA: OngoingClover Hill Dairy, LLC
FoodAug 12, 2026
PT Organics Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit recall — FDA H-1223-2026
Possible foreign object (thin, soft plastic strands).
Class IIFDA: OngoingPT Organics Limited
FoodAug 12, 2026
Clover Hill Dairy Pepper Jack Cheese recall — FDA H-1214-2026
Product contaminated with Listeria monocytogenes.
Class IFDA: OngoingClover Hill Dairy, LLC
FoodAug 12, 2026
Clover Hill Dairy Mild Cheese recall — FDA H-1205-2026
Product contaminated with Listeria monocytogenes.
Class IFDA: OngoingClover Hill Dairy, LLC
FoodAug 12, 2026
FACTORY6 Zen Principle Naturals Moringa Leaf Powder dietary supplement recall — FDA H-1222-2026
Possible Salmonella in Moringa Leaf Powder product.
Class IFDA: OngoingFACTORY6, Inc.
FoodAug 12, 2026
Clover Hill Dairy Pepper Jack Cheese recall — FDA H-1213-2026
Product contaminated with Listeria monocytogenes.
Class IFDA: OngoingClover Hill Dairy, LLC
FoodAug 12, 2026
M.G. Foods Spicy Breakfast Burrito sold under the following brand names recall — FDA H-1192-2026
Undeclared Soy. The firm received complaints of sausage in the burritos. Upon review the firm discovered the sausage contains soy which is not listed on the label.
Class IFDA: OngoingM.G. Foods, Inc.
FoodAug 12, 2026
Clover Hill Dairy mild cheese recall — FDA H-1206-2026
Product contaminated with Listeria monocytogenes.
Class IFDA: OngoingClover Hill Dairy, LLC
VehicleAug 6, 2026
Toyota Motor Engineering & Manufacturing shock absorber recall — NHTSA campaign 26V514000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2024 Tacoma Hybrid and 2024-2025 Tacoma vehicles. The metal flange on the front and rear shock absorbers may corrode…
shock absorberToyota Motor Engineering & Manufacturing
VehicleAug 5, 2026
Tesla headlights recall — NHTSA campaign 26V507000
Tesla, Inc. (Tesla) is recalling certain 2017-2023 Model 3 and 2020-2023 Model Y vehicles. The headlight low beams may be too bright and exceed the maximum light output. As such, these…
headlightsTesla, Inc.
Medical DeviceAug 5, 2026
GEM Premier 5000 recall — FDA Z-2826-2026
Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.
Class IIFDA: OngoingInstrumentation Laboratory
Medical DeviceAug 5, 2026
Argon Medical Devices L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) recall — FDA Z-2803-2026
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or…
Class IIFDA: OngoingArgon Medical Devices, Inc
Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 60mm recall — FDA Z-2830-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
Medical DeviceAug 5, 2026
Medtronic Perfusion Systems EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended recall — FDA Z-2807-2026
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation,…
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceAug 5, 2026
Instrumentation Laboratory GEM Premier 5000 with IQM2 recall — FDA Z-2821-2026
Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.
Class IIFDA: OngoingInstrumentation Laboratory
Medical DeviceAug 5, 2026
Windstone Medical Packaging AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled recall — FDA Z-2802-2026
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed Neurological Sponges Non-Sterile Models 55992C to 55998C due to…
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceAug 5, 2026
Windstone Medical Packaging AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled recall — FDA Z-2815-2026
Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris…
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceAug 5, 2026
Windstone Medical Packaging AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled recall — FDA Z-2813-2026
Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris…
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceAug 5, 2026
Medical Action Industries, Inc. 306 Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I recall — FDA Z-2792-2026
Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood…
Class IFDA: OngoingMedical Action Industries, Inc. 306
Medical DeviceAug 5, 2026
Permobil M5 Corpus Power Wheelchair REF,120032 recall — FDA Z-2805-2026
This recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic. This issue may allow the chair to drive under restricted conditions, and may…
Class IIFDA: OngoingPermobil Inc
Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 50mm recall — FDA Z-2829-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
Medical DeviceAug 5, 2026
PHILIPS MEDICAL SYSTEMS Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro CT5000 recall — FDA Z-2652-2026
The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result in the…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS
Medical DeviceAug 5, 2026
Windstone Medical Packaging AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled recall — FDA Z-2812-2026
Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris…
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
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.