FoodMay 13, 2026
Silver Moon LP dba Loard's Ice Cream Banana Ice Cream - 32 oz recall — FDA H-0756-2026
Undeclared Yellow #5
Class IIFDA: OngoingSilver Moon LP dba Loard's Ice Cream
May 2026 recalls — page 11
These records include useful source details for the selected month.
VehicleMay 12, 2026
Bronco roof and pillars recall — NHTSA campaign 26V299000
Ford Motor Company (Ford) is recalling certain 2021-2022 Bronco vehicles. The 3-door and 5-door Molded-In-Color (MIC) hardtop roof panels may have been manufactured improperly, which can…
roof and pillarsFord Motor Company
VehicleMay 12, 2026
Ford park pawl recall — NHTSA campaign 26V301000
Ford Motor Company (Ford) is recalling certain 2026 Escape and Lincoln Corsair vehicles. The integrated park module may fail to lock into the park position when the driver shifts into park.…
park pawlFord Motor Company
VehicleMay 7, 2026
Chrysler control module (tcm/pcm/tecm) recall — NHTSA campaign 26V288000
Chrysler (FCA US LLC) is recalling certain 2023-2026 Ram 2500 Pick up trucks. A software error in the powertrain control module may improperly allow the vehicle speed to exceed the tire…
control module (tcm/pcm/tecm)Chrysler (FCA US, LLC)
VehicleMay 7, 2026
Jeep Cherokee powertrain recall — NHTSA campaign 26V290000
Chrysler (FCA US LLC) is recalling certain 2019-2023 Jeep Cherokee vehicles. The power transfer unit (PTU) may fail.
powertrainChrysler (FCA US, LLC)
VehicleMay 7, 2026
General Motors transfer case (4-wheel drive) recall — NHTSA campaign 26V289000
General Motors, LLC (GM) is recalling certain 2026 Cadillac Escalade and Escalade ESV, Chevrolet Silverado 1500, Suburban, and Tahoe, and GMC Sierra 1500, Yukon, and Yukon XL vehicles with…
transfer case (4-wheel drive)General Motors, LLC
Medical DeviceMay 6, 2026
Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1 recall — FDA Z-1965-2026
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel…
Class IIFDA: OngoingPhilips North America
Medical DeviceMay 6, 2026
Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1 recall — FDA Z-1967-2026
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel…
Class IIFDA: OngoingPhilips North America
Medical DeviceMay 6, 2026
Medline and Centurion medical procedure kits, containing Medline Neuro Sponges recall — FDA Z-2021-2026
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMay 6, 2026
Philips Ingenia Ambition X with MR Elastography (MRE). 1 recall — FDA Z-1961-2026
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel…
Class IIFDA: OngoingPhilips North America
Medical DeviceMay 6, 2026
Philips Upgrade to MR 7700 with MR Elastography (MRE). 1 recall — FDA Z-1969-2026
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel…
Class IIFDA: OngoingPhilips North America
Medical DeviceMay 6, 2026
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1 recall — FDA Z-2036-2026
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMay 6, 2026
Medline medical procedure kits, containing Medline Neuro Sponges (102 in total) recall — FDA Z-2025-2026
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMay 6, 2026
Disposable Mixing Bowls with Spatula Mixing Bowl and Spatula recall — FDA Z-1946-2026
Ten complaints have been received identifying issues at the time of use related to the package seal, including incomplete seals, wrinkles in the seals or peeling seals. Compromised sterile…
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceMay 6, 2026
Kiwi Omni Vacuum Delivery System recall — FDA Z-1945-2026
Due to complaints of device breakage at the traction force gauge to handle joint.
Class IIFDA: OngoingClinical Innovations, LLC
Medical DeviceMay 6, 2026
Medline Industries Centurion medical procedure kits, containing Medline Neuro Sponges recall — FDA Z-2028-2026
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMay 6, 2026
Philips Ingenia Elition S with MR Elastography (MRE). 1 recall — FDA Z-1962-2026
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel…
Class IIFDA: OngoingPhilips North America
Medical DeviceMay 6, 2026
Abbott Point Of Care i-STAT EG6+ cartridge recall — FDA Z-2000-2026
Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26) cartridge lots in the U.S.…
Class IIFDA: OngoingAbbott Point Of Care Inc.
Medical DeviceMay 6, 2026
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1 recall — FDA Z-2019-2026
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMay 6, 2026
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: EH recall — FDA Z-2010-2026
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMay 6, 2026
Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1 recall — FDA Z-1954-2026
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel…
Class IIFDA: OngoingPhilips North America
Medical DeviceMay 6, 2026
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1 recall — FDA Z-2015-2026
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMay 6, 2026
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1 recall — FDA Z-2024-2026
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMay 6, 2026
Medline Industries Centurion medical convenience kits, containing Webcol Large Alcohol Prep recall — FDA Z-2044-2026
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large…
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.