Medical DeviceJul 9, 2025
Philips V6-2 Transducer recall — FDA Z-2062-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
July 2025 recalls — page 9
These records include useful source details for the selected month.
Medical DeviceJul 9, 2025
Philips X8-2t Transducer recall — FDA Z-2067-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
HemoCue AB The HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue recall — FDA Z-2070-2025
Glucose microcuvettes experienced transit time outside of limits, so stability through the whole microcuvette lifetime can no longer be guaranteed. The affected products may not have been…
Class IIFDA: OngoingHemoCue AB
Medical DeviceJul 9, 2025
Philips X6-1 Transducer recall — FDA Z-2065-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips L12-3 Transducer recall — FDA Z-2054-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips C5-2 Transducer recall — FDA Z-2050-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips Respironics BiPAP A40 Ventilator recall — FDA Z-2037-2025
This device does not indicate for use in patients with respiratory failure.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceJul 9, 2025
Philips eL18-4 Transducer recall — FDA Z-2052-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
CORIN MEDICAL Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117 recall — FDA Z-2069-2025
Investigation has identified that the age of the nylon packaging material has caused a loss of integrity of some pouches.
Class IIFDA: OngoingCORIN MEDICAL, LTD.
Medical DeviceJul 9, 2025
Maquet Critical Care AB Servo-u Ventilator System recall — FDA Z-2013-2025
Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active…
Class IFDA: OngoingMaquet Critical Care AB
Medical DeviceJul 9, 2025
Change Healthcare Cardiology Hemodynamics Software recall — FDA Z-2072-2025
Due to complaints, software update may cause software to unexpectedly shutdown.
Class IIFDA: OngoingCHANGE HEALTHCARE CANADA COMPANY
Medical DeviceJul 9, 2025
Philips C9-5EC Transducer recall — FDA Z-2051-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Becton, Dickinson and Company, BD Bio Sciences REF: 666289 , BD FACS, 7-Color Setup Beads recall — FDA Z-2079-2025
Due to customer complaints, errors in spectral overlap factors table for 7-color setup beads may affect accurate setup of the flow cytometry instrument prior to analyzing samples.
Class IIFDA: OngoingBecton, Dickinson and Company, BD Bio Sciences
Medical DeviceJul 9, 2025
Philips eL18-4 EMT Transducer recall — FDA Z-2053-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
FoodJul 9, 2025
Harris Teeter ZENSHI HANDCRAFTED SUSHI Premium Chef Sampler #1 recall — FDA H-0178-2025
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Class IFDA: TerminatedHarris Teeter
FoodJul 9, 2025
Harris Teeter ZENSHI HANDCRAFTED SUSHI Hawaiian Roll - Salmon, Tuna 10pc Net recall — FDA H-0166-2025
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Class IFDA: TerminatedHarris Teeter
FoodJul 9, 2025
Harris Teeter ZENSHI HANDCRAFTED SUSHI Vegetable Roll 10pc recall — FDA H-0199-2025
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Class IFDA: TerminatedHarris Teeter
FoodJul 9, 2025
Harris Teeter ZENSHI HANDCRAFTED SUSHI Hybrid Roku Tray 82pc Net Wt recall — FDA H-0173-2025
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Class IFDA: TerminatedHarris Teeter
FoodJul 9, 2025
Harris Teeter ZENSHI HANDCRAFTED SUSHI Crunchy Shrimp Tempura Roll 10pc recall — FDA H-0148-2025
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Class IFDA: TerminatedHarris Teeter
FoodJul 9, 2025
Harris Teeter ZENSHI HANDCRAFTED SUSHI Chile Serrano Roll 10pc Sushi Net Wt recall — FDA H-0132-2025
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Class IFDA: TerminatedHarris Teeter
FoodJul 9, 2025
Harris Teeter ZENSHI HANDCRAFTED SUSHI Ultimate Chili Roll - Tuna 10pc Net recall — FDA H-0197-2025
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Class IFDA: TerminatedHarris Teeter
FoodJul 9, 2025
Harris Teeter ZENSHI HANDCRAFTED SUSHI Mango Crunchy Dragon Roll 10pc Net Wt recall — FDA H-0176-2025
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Class IFDA: TerminatedHarris Teeter
FoodJul 9, 2025
Harris Teeter ZENSHI HANDCRAFTED SUSHI Yuzu Teriyaki Sauce 3oz Net Wt recall — FDA H-0200-2025
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Class IFDA: TerminatedHarris Teeter
FoodJul 9, 2025
Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans recall — FDA H-0203-2025
Overpressurization leading to exploding cans
Class IIFDA: TerminatedPeak Cocktails
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.