FoodJun 25, 2025
GBC Food Services Cucumber Bowl with Ranch dip 15oz UPC 850054894519 Purchase recall — FDA H-0052-2025
Potential to be contaminated with Salmonella
Class IFDA: OngoingGBC Food Services, LLC
June 2025 recalls — page 2
These records include useful source details for the selected month.
FoodJun 25, 2025
Yerba Prima Great Plains Bentonite + Herbal Detox Capsules 60 capsules recall — FDA H-0050-2025
Potential contamination with Pseudomonas aeruginosa.
Class IIFDA: TerminatedYerba Prima Inc.
FoodJun 25, 2025
La Fontanella Food Products net wt recall — FDA H-0051-2025
Potential for product spoilage (increased level of lactic acid detected in retain samples).
Class IIFDA: TerminatedLa Fontanella Food Products LLC
FoodJun 25, 2025
Ariana Sweets AFGHANI CORN BREAD "Doda" recall — FDA F-0938-2025
Undeclared allergens (wheat, sesame)
Class IFDA: TerminatedAriana Sweets Inc.
FoodJun 25, 2025
GBC Food Services Chef Salad 11oz 850065403328 Purchase Dates: 05/08/2025 to recall — FDA H-0054-2025
Potential to be contaminated with Salmonella
Class IFDA: OngoingGBC Food Services, LLC
FoodJun 25, 2025
The Coca-Cola Company Topo Chico MINERAL WATER CARBONATED 16.9 FL OZ recall — FDA H-0048-2025
Pseudomonas in Mineral Water. The firm was notified by their distributor that product placed on hold was released and shipped to customers.
Class IIFDA: CompletedThe Coca-Cola Company
FoodJun 25, 2025
RGB Soda, LLC Refrigerated Cucumber X Tarragon Ginger Beer recall — FDA H-0057-2025
Potential contamination with Salmonella.
Class IFDA: TerminatedRGB Soda, LLC.
DrugJun 25, 2025
Umary-USA.com UMOVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN recall — FDA D-0493-2025
Marketed without approved NDA/ANDA- Laboratory analysis found product to be tainted with undeclared ingredients: Dexamethasone and Diclofenac.
Class IFDA: CompletedUmary-USA.com
DrugJun 25, 2025
Gentamicin Injection, USP, (PEDIATRIC), 20 mg per 2 mL (10 mg per mL*), 2 mL Single-Dose recall — FDA D-0472-2025
Failed Stability Specifications: Out of specification results for the Color Absorbance test during 12 Month sample analysis.
Class IIFDA: OngoingEugia US LLC
DrugJun 25, 2025
Umary-USA.com UNAVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN recall — FDA D-0492-2025
Marketed without approved NDA/ANDA- Laboratory analysis found product to be tainted with undeclared ingredients: Dexamethasone, Diclofenac and Omeprazole.
Class IFDA: CompletedUmary-USA.com
VehicleJun 19, 2025
Forester child seat recall — NHTSA campaign 25V419000
Subaru of America, Inc. (Subaru) is recalling certain 2025 Forester vehicles. The child seat anchor bolts may have been improperly tightened, allowing the bolts to come loose.
child seatSubaru of America, Inc.
Medical DeviceJun 18, 2025
BD SWITZERLAND SARL BD Texium: 3 mL, REF: MY8003-0006 recall — FDA Z-1972-2025
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
American Contract Systems LOWER EXTREMITY, Model: NCEX20I recall — FDA Z-1916-2025
Test results for cast padding component included in procedure trays shows Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals exceeded residual limits, which may lead to a possible loss…
Class IIFDA: OngoingAmerican Contract Systems, Inc.
Medical DeviceJun 18, 2025
Powered Laser Surgical Instrument SOLTIVE Pro SuperPulsed Laser System recall — FDA Z-1920-2025
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
Philips Achieva XR Product Numbers: (1) 781153, (2) 781253 recall — FDA Z-1928-2025
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
Guardian System 2 Controller recall — FDA Z-1968-2025
A software update corrected an issue where "low" and "terminal" battery alerts did not display on the screen to the user in specific circumstances when the device was not running patient…
Class IIFDA: OngoingTurncare, Inc.
Medical DeviceJun 18, 2025
Powered Laser Surgical Instrument Soltive Reusable Laser Fibers recall — FDA Z-1923-2025
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
Tecfen Medical 2.4mm Slit Knife, Angled recall — FDA Z-1951-2025
Sterility assurance for Ophthalmic knives.
Class IIFDA: OngoingTecfen Medical
Medical DeviceJun 18, 2025
Powered Laser Surgical Instrument SOLTIVE Premium SuperPulsed Laser System recall — FDA Z-1921-2025
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
Philips Intera 1.5T Omni/Stellar recall — FDA Z-1934-2025
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
Solana Bordetella kit recall — FDA Z-1948-2025
It was determined that there could be a false positive rate of up to 16.7% for the affected lots associated with the Bordetella parapertussis (BPP) results (only) of the assay.
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJun 18, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Azurion R1.x and R2.x systems recall — FDA Z-1969-2025
A software issue was identified in the internal communication process between the system software and the X-ray generator firmware. Loss of imaging (X-ray) functionality caused by the…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceJun 18, 2025
Tecfen Medical 2.2mm Slit Knife, Angled recall — FDA Z-1950-2025
Sterility assurance for Ophthalmic knives.
Class IIFDA: OngoingTecfen Medical
Medical DeviceJun 18, 2025
Philips Intera 1.5T Master/Nova Product Number: 781106 recall — FDA Z-1933-2025
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
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.