FoodJul 30, 2025
Mondelez Global Ritz Peanut Butter Cracker Sandwiches, Net Wt recall — FDA H-0326-2025
Undeclared allergens (Peanut) due to mispackaging
Class IIFDA: OngoingMondelez Global LLC
Latest records
Latest recalls — page 194
The newest recall records with useful source details are listed here.
FoodJul 30, 2025
Gedney Foods Product Zinger Pickle products under the following labels: 1 recall — FDA H-0329-2025
Products were slated for disposal due to product and container damage, but were inadvertently sold.
Class IIFDA: TerminatedGedney Foods Product, LLC
DrugJul 30, 2025
clomiPRAMINE Hydrochloride Capsules USP 25 mg, 100 count bottles, 5801 Pelican Bay recall — FDA D-0537-2025
Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during retention sample testing at…
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugJul 30, 2025
Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per recall — FDA D-0541-2025
Lack of Assurance of Sterility: A market complaint was received for leakage and empty ampoule.
Class IIFDA: OngoingCipla USA, Inc.
VehicleJul 28, 2025
Telluride exterior trim recall — NHTSA campaign 25V494000
Kia America, Inc. (Kia) is recalling certain 2023-2025 Telluride vehicles. The door belt molding trim can delaminate and detach from the vehicle.
exterior trimKia America, Inc.
VehicleJul 25, 2025
Ford control module software recall — NHTSA campaign 25V488000
Ford Motor Company (Ford) is recalling certain 2025 Lincoln Navigator, F-150, Expedition, Bronco, and Ranger vehicles. The Electronic Brake Booster (EBB) module may malfunction while…
control module softwareFord Motor Company
Medical DeviceJul 23, 2025
Ortho-Clinical Diagnostics VITROS Chemistry Products CHE Slides (Japan) recall — FDA Z-2123-2025
Quality control (QC) drift when certain lots of Performance Verifiers (PVs) are used with certain lots of cholinesterase enzyme (CHE) slides. This drift occurs when the PVs are used 2-7…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 23, 2025
Microbiologics KWIK-STIK and LYFO DISK, quality control kit for culture media Catalog # recall — FDA Z-2124-2025
Affected products contain Staphylococcus epidermidis instead of the expected Brevundimonas diminuta. This may cause the user's quality control to fail and delayed diagnosis for the patient.
Class IIFDA: OngoingMicrobiologics Inc.
Medical DeviceJul 23, 2025
Ortho-Clinical Diagnostics VITROS Chemistry Products CHE Slides recall — FDA Z-2122-2025
Quality control (QC) drift when certain lots of Performance Verifiers (PVs) are used with certain lots of cholinesterase enzyme (CHE) slides. This drift occurs when the PVs are used 2-7…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 23, 2025
Beyond Laser Systems Laser light show projectors manufactured by BLS, Model PURE 5000/10000 recall — FDA Z-2113-2025
The remote interlock connector, which is required by 21 CFR 1040.10(f)(3), in the remote stop box was not installed the connector or was mechanically installed but not wired. The labels…
Class IIFDA: OngoingBeyond Laser Systems, LLC
Medical DeviceJul 23, 2025
Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2 recall — FDA Z-2096-2025
Certain Spectrum infusion pumps may have an incorrect version of software.
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 23, 2025
Medtronic SmartLink software loaded on CareLink SmartSync Device Manager, Model Number recall — FDA Z-2128-2025
A software update for Medtronic CareLink SmartSync Device Manager (SmartSync) is now available. The update eliminates the potential display of an erroneous electrical reset (pop-up) message…
Class IIFDA: OngoingMedtronic, Inc.
Medical DeviceJul 23, 2025
Beyond Laser Systems Laser light show projectors manufactured by BLS, Model DIODE recall — FDA Z-2111-2025
The remote interlock connector, which is required by 21 CFR 1040.10(f)(3), in the remote stop box was not installed the connector or was mechanically installed but not wired. The labels…
Class IIFDA: OngoingBeyond Laser Systems, LLC
Medical DeviceJul 23, 2025
VITROS Chemistry Products Performance Verifier II recall — FDA Z-2121-2025
Quality control (QC) drift when certain lots of Performance Verifiers (PVs) are used with certain lots of cholinesterase enzyme (CHE) slides. This drift occurs when the PVs are used 2-7…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 23, 2025
VITROS Chemistry Products Performance Verifier I recall — FDA Z-2120-2025
Quality control (QC) drift when certain lots of Performance Verifiers (PVs) are used with certain lots of cholinesterase enzyme (CHE) slides. This drift occurs when the PVs are used 2-7…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 23, 2025
Beyond Laser Systems Laser light show projectors manufactured by BLS, Model CLUB recall — FDA Z-2112-2025
The remote interlock connector, which is required by 21 CFR 1040.10(f)(3), in the remote stop box was not installed the connector or was mechanically installed but not wired. The labels…
Class IIFDA: OngoingBeyond Laser Systems, LLC
Medical DeviceJul 23, 2025
Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX recall — FDA Z-2095-2025
Certain Spectrum infusion pumps may have an incorrect version of software.
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 23, 2025
Beckman Coulter Access Vitamin B12 Reagent, Catalog Number 33000, Lot Number 439850 recall — FDA Z-2115-2025
Beckman Coulter has received complaints of erroneous Vitamin B12 results when using Access Vitamin B12 Reagent lot 439850. The affected reagent lot may cause erroneously low or high Vitamin…
Class IIFDA: CompletedBeckman Coulter, Inc.
Medical DeviceJul 23, 2025
EMPOWR 3D KNEETM INS, 11L 10MM, VE recall — FDA Z-2125-2025
Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. The use of this product may result in the incorrect product being selected. This could result in a…
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJul 23, 2025
NeuroSync EYE-SYNC containing Pico Neo 2 Headsets recall — FDA Z-2114-2025
Eye syncing issues causing the device to be inoperable. Unable to be repaired due to discontinuation of support for the Pico 2 platform, which was no longer in production or serviceable as…
Class IIFDA: OngoingNeuroSync, Inc.
Medical DeviceJul 23, 2025
NIO-A NIO Intraosseous Device Adult recall — FDA Z-2118-2025
Due to manufacturing error, Intraosseous device built-in stabilizer may not be released properly after deployment and insertion.
Class IIFDA: OngoingWaismed Ltd.
Medical DeviceJul 23, 2025
NIO+ NIO Intraosseous Device Adult recall — FDA Z-2119-2025
Due to manufacturing error, Intraosseous device built-in stabilizer may not be released properly after deployment and insertion.
Class IIFDA: OngoingWaismed Ltd.
Medical DeviceJul 23, 2025
Intersurgical i-view video laryngoscope recall — FDA Z-2102-2025
Potential for faulty devices as a result of depleted batteries.
Class IFDA: OngoingIntersurgical Inc.
Medical DeviceJul 23, 2025
Medtronic SmartLink Software loaded on SmartSync Patient Connector, Model Number 24967 with recall — FDA Z-2127-2025
A software update for Medtronic CareLink SmartSync Device Manager (SmartSync) is now available. The update eliminates the potential display of an erroneous electrical reset (pop-up) message…
Class IIFDA: OngoingMedtronic, Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026361 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories