Recalls affecting Minnesota
Notices that name Minnesota in their distribution area, plus every nationwide recall — nationwide recalls reach Minnesota too.
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Class II · 12 months ago
Daye Heavy Flow Bundle recall: Product lacks 510(k) clearance
Product lacks 510(k) clearance.
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Class II · 12 months ago
Daye Initiation 3 Month Regular Flow Bundle recall: Product lacks 510(k) clearance
Product lacks 510(k) clearance.
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Class I · 12 months ago
Brand Name: Dexcom G6 Continuous Glucose Monitoring System Product recall: A software defect in version v1.15.0 of the G6 Android app can cause the app
A software defect in version v1.15.0 of the G6 Android app can cause the app to terminate unexpectedly, which may result in the user not receiving…
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Class II · 12 months ago
ICU Medical Oncology Kit w/ChemoLock, ChemoLock Port REF: CL4136 recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class II · 12 months ago
Daye Trial Tampon Box recall: Product lacks 510(k) clearance
Product lacks 510(k) clearance.
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Class II · 12 months ago
Surgical Navigation Advanced Platform , software version SNP.3.12.0 recall: A software anomaly, under specific conditions when large rotational alignment
A software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any…
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Class II · 12 months ago
Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices recall: Due to incomplete seals in the pouch which provide the sterile barrier
Due to incomplete seals in the pouch which provide the sterile barrier.
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Class II · 12 months ago
Daye Initiation 36 Coated Super Tampons recall: Product lacks 510(k) clearance
Product lacks 510(k) clearance.
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Class II · 12 months ago
ICU Medical ChemoLock Bag Spike REF: CL-10 recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class II · 12 months ago
ICU Medical 45" Appx 1.7 ml, Smallbore Ext Set w/Spiros w/Red Cap recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class II · 12 months ago
Daye Initiation 3 Month All in One Bundle recall: Product lacks 510(k) clearance
Product lacks 510(k) clearance.
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Class II · 12 months ago
ICU Medical ChemosafeLock Bag Spike REF: KL-BS001U3 recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class II · 12 months ago
Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices recall: Due to incomplete seals in the pouch which provide the sterile barrier
Due to incomplete seals in the pouch which provide the sterile barrier.
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Class II · 12 months ago
ICU Medical Double ChemoLock Port Syringe Transfer Set REF: CL-33 recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class II · 12 months ago
ICU Medical Oncology Kit w/2 ChemoLock", 13mm Closed Vial Spike recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class II · 12 months ago
ICU Medical ChemoLock Port REF: CL2100 recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class II · 12 months ago
Anatomy Supply Partners, LLC. Safe-T-Fill Micro Capillary Blood Collection recall: All RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured
All RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured between July 31, 2023 to February 28, 2025 cause false positive results when…
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Class II · 12 months ago
CareFusion 303, Inc. Various models of BD Pyxis MedFlex recall: Potential fluid ingress of anesthesia station or med station may result
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
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Class II · 12 months ago
ICU Medical Clave Bag Spike w/ChemoLock Port REF: CL2150 recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class II · 12 months ago
ICU Medical Graduated Connector w/ChemoLock Port REF: CL3900 recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class II · 12 months ago
ICU Medical ChemoLock Vial Spike, 20mm REF: CL-80S recall: Port weld of drug transfer device may separate or break during use
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
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Class II · 12 months ago
Brand Name: Medistim MiraQ System Product Name: Medistim MiraQ System recall: Printer Support Module (PSM) may be subject to insufficient soldering
Printer Support Module (PSM) may be subject to insufficient soldering, which may cause loosening of the wires and system to shut down. Affected…
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Class II · 12 months ago
Brand Name: Aesculap Product Name: Reducing Converter 10/12MM TO 5MM recall: It was determined there is the potential of silicone fragments detaching
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
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Class II · 12 months ago
SpineAR Surgical Navigation Advanced Platform Patient Engagement recall: A software anomaly, under specific conditions when large rotational alignment
A software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any…