Medical DeviceJun 18, 2025
Remel Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ recall — FDA Z-1947-2025
Product may have an off color affecting perfomance
Class IIFDA: OngoingRemel, Inc.
June 2025 recalls — page 4
These records include useful source details for the selected month.
Medical DeviceJun 18, 2025
QUANTUM SURGICAL SAS EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE device is a recall — FDA Z-1927-2025
Due to a software bug the robotic arm may incorrectly guide the instrument compared to the planning defined by user.
Class IIFDA: OngoingQUANTUM SURGICAL SAS
Medical DeviceJun 18, 2025
BD SWITZERLAND SARL BD Texium Needle-Free Syringe: 3 mL, REF: MY8003 recall — FDA Z-1971-2025
Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the…
Class IIFDA: OngoingBD SWITZERLAND SARL
Medical DeviceJun 18, 2025
Medtronic Azure S DR MRI SureScan, Product number W3DR01 recall — FDA Z-1924-2025
Identified devices may experience sudden battery power failure without alarm, power supply power-on-resets, and interruption of therapy. Potential patient harms include insufficient pacing…
Class IIFDA: OngoingMedtronic, Inc.
Medical DeviceJun 18, 2025
Powered Laser Surgical Instrument Soltive SuperPulsed Laser Fibers - Single Use recall — FDA Z-1922-2025
Potential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use. The fracturing of the fiber is the cause of, or…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceJun 18, 2025
SmartRelease ESTR recall — FDA Z-1975-2025
Potential that the blade can unintentionally cut tissue prior to the user deploying the blade.
Class IIFDA: OngoingMicroAire Surgical Instruments, LLC
Medical DeviceJun 18, 2025
Mobius Mobility iBOT PMD with software version 01.05.24 recall — FDA Z-1965-2025
Software issue that could potentially lead to the device tipping over from Balance Mode.
Class IIFDA: OngoingMobius Mobility LLC
Medical DeviceJun 18, 2025
Microbiologics KWIK-STICK, Quality control kit for culture media, Catalog Numbers 01065K recall — FDA Z-1957-2025
Affected products were packaged with the incorrect KWIK STIK assembly resulting in the product containing the wrong microorganism. 0621K was packaged 01065K swabs; 01065K was packaged with…
Class IIFDA: OngoingMicrobiologics Inc.
Medical DeviceJun 18, 2025
BD SWITZERLAND SARL BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241-0500 recall — FDA Z-1973-2025
Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the…
Class IIFDA: OngoingBD SWITZERLAND SARL
Medical DeviceJun 18, 2025
Tecfen Medical 3.2mm Slit Knife, Angled recall — FDA Z-1955-2025
Sterility assurance for Ophthalmic knives.
Class IIFDA: OngoingTecfen Medical
Medical DeviceJun 18, 2025
Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI recall — FDA Z-1963-2025
Due to non-sterile products being labeled as sterile
Class IIFDA: OngoingMicrotek Medical, Inc.
Medical DeviceJun 18, 2025
Philips Intera 1.5T Achieva Nova-Dual Product Number: 781173 recall — FDA Z-1931-2025
identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If…
Class IIFDA: OngoingPhilips North America
Medical DeviceJun 18, 2025
Fresenius Kabi USA IVENIX INFUSION SYSTEM LVP Blood Products Administration Set, Dual-Inlet recall — FDA Z-1869-2025
Mis-assembly error of Blood Products Administrations Sets where the 200-micron drip chamber filter may be incorrectly positioned and unable to filter out large blood particulates.
Class IFDA: OngoingFresenius Kabi USA, LLC
Medical DeviceJun 18, 2025
OBM00002 OBM DAB (Digital Acquisition Box) recall — FDA Z-1925-2025
Electrode placement labels on the Digital Acquisition Box (DAB) were applied backwards. This may ultimately lead to misdiagnosis of seizure location in neonates monitored with this device.
Class IIFDA: OngoingNatus Neurology DBA Excel Tech., Ltd. (XLTEK)
Medical DeviceJun 18, 2025
GE Medical Systems OEC Elite: The OEC Elite mobile C-arm is intended to provide fluoroscopic recall — FDA Z-1819-2025
OEC Elite and OEC 3D Mobile C-Arms Exceeding 4% Source to Image Distance in X-ray Field.
Class IIFDA: OngoingGE Medical Systems, LLC
VehicleJun 18, 2025
Mazda North American Operations air bag control module software recall — NHTSA campaign 25V413000
Mazda North American Operations (Mazda) is recalling certain CX-50 Hybrid and CX-50 vehicles. Incorrectly configured module software may cause the air bag to deploy improperly.
air bag control module softwareMazda North American Operations
FoodJun 18, 2025
Sysco HKSAN167 1/5.76 OZ recall — FDA H-0021-2025
Cucumbers have the potential to be contaminated with Salmonella
Class IFDA: TerminatedSysco Corporation
FoodJun 18, 2025
Unilever Manufacturing (US) Rocky Road Ice Cream packaged in a Breyer Chocolate Truffle recall — FDA H-0017-2025
Undeclared allergens and mislabeled product. Rocky Road Ice was packaged with Chocolate Truffle Ice Cream labeled tub and a Rocky Road Ice Cream lid. Tub said "may contain tree nuts" the…
Class IIFDA: TerminatedUnilever Manufacturing (US), Inc.
FoodJun 18, 2025
R&M TRADING Instant Milk Tea Taro Flavor, R&M Refresher brand, B0D72CMLBH recall — FDA F-0932-2025
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Class IIIFDA: TerminatedR&M TRADING LLC
FoodJun 18, 2025
Comvita branded Manuka Honey + Cordyceps for energy recall — FDA H-0015-2025
Leaking induction seal on packaging.
Class IIFDA: TerminatedCOMVITA USA Inc.
FoodJun 18, 2025
Sysco 5185 2/7.125# EAST COAST FRESH AUTHENTIC GREEK SALAD recall — FDA H-0019-2025
Cucumbers have the potential to be contaminated with Salmonella
Class IFDA: TerminatedSysco Corporation
FoodJun 18, 2025
R&M TRADING Instant Milk Tea Matcha Flavor, R&M Refresher brand recall — FDA F-0933-2025
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Class IIIFDA: TerminatedR&M TRADING LLC
FoodJun 18, 2025
Sysco HKSAC168 6/5.76 OZ recall — FDA H-0020-2025
Cucumbers have the potential to be contaminated with Salmonella
Class IFDA: TerminatedSysco Corporation
FoodJun 18, 2025
Post Honey Bunches of Oats with Almonds recall — FDA H-0044-2025
Foreign Material (metal)
Class IIFDA: TerminatedPost Consumer Brands, LLC
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.