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All product recalls affecting North Carolina.
Includes nationwide recalls (tagged “Nationwide”) and recalls with North Carolina in the distribution area.
This recall involves Style Life Eleven baby loungers. The loungers include a head pillow and fold into a portable handbag with a handle. When folded into the portable handbag, the brand name "Style Life Eleven" is visible on a white square in cursive font. The loungers were sold in different printed fabrics including Dinosaur, Blue & White Crowns, Dotted Pink, Dotted White & Purple, Zoo Animals, and Gray & Brown Crowns. Only portable loungers purchased on or after June 23, 2022, are included in this recall.
This recall involves TRUBLUE iQ Auto Belay Devices, which enable climbers to safely descend while climbing. The TRUBLUE iQ is gray with blue handles and a gray sash on the front cover. The TRUBLUE iQ+ has an added catch-and-hold brake on the front. The LT versions of the iQ and iQ+ have blue tags above the blue webbing hand grip; the XL versions have a purple tag. The recalled auto belay devices have a serial number within the following serial number ranges printed on the device's handle, as well on the bottom of the device: Products Models Serial Number Range TRUBLUE iQ LT TBiQ LT (12.5m) iQ0041591 through iQ0044486 TRUBLUE iQ+LT TBiQ+ LT (12.5m) iQP000401 through iQP000422 TRUBLUE iQ XL TBiQ XL (20m) iQXL01283 through iQXL03425 TRUBLUE iQ+XL TBiQ+ XL (20m) iQXLP0104 through iQXLP0215
The hardness not meeting the material specification and may cause the diamond bur to bend.
Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.
Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.
Orange EV is recalling certain 2023-2024 HUSK-e XP terminal trucks. The rear Gross Axle Weight Rating (GAWR) on the federal placard is incorrect and the installed tires and rims may be inadequate for the truck's intended use. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 120, "Wheels and Rims - Other Than Passenger Cars."
Due to an increase in complaints concerning foot tray pedal spring failing resulting in the pedal remaining pressed
Aspiration catheter distal tip features and characteristics may not be in the scope of FDA clearance; tip detachment, vessel rupture, and vasospasm could occur.
Beckman Coulter has determined that device software versions V1.3, V1.4, V1.4.1, V1.4.2, V1.4.3. have a defect due of which, when all constituent tests of a calculated result are rerun, either manually ordered by the operator at the analyzer or automatically triggered by predefined rules in System Configuration, the calculated result will not be recalculated using the constituent tests rerun results. The system will report only the calculated result using the initial constituent tests results to the operator and LIS/Remisol. The issue was identified by Beckman Coulter internal engineering testing. The defect may cause a delay in reporting patient results.
Tracheostomy tube with cuff reusable inner cannula has a flange that may disconnect from the outer cannula of the device, which could cause respiratory failure, aspiration, unspecified tissue injury, aspiration, respiratory tract infection, bronchospasm, a delay to treatment and/or death.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
A wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.