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All product recalls affecting Texas.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Texas in the distribution area.
This recall involves ARVA Neo BT Pro Avalanche Transceivers. The transceivers are black plastic with an LCD screen below a red mark button. NEO BT PRO is written on the left side of the device. The affected beacons have serial numbers NBP00052-1027 to NBP00287-1127 and NB00300-1127 to NB11675-0329. The serial number is located inside the battery compartment on the underside of the battery compartment lid.
The recalled Prestige Solo, Prestige Excellence, and Aerco Esteem boilers are wall-hung condensing gas boilers housed in a white metal box. "Prestige" is printed on the white front panel of the recalled Prestige Solo and Prestige Excellence boilers. "Aerco" is printed on the front of the recalled Esteem boilers. Please visit the Triangle Tube recall website for directions on identifying if you have a recalled boiler by serial number, which can be located either on the Boiler Rating Label located on the white front panel, on a panel on the right hand side of the boiler, or behind the boiler front door. The following models and serial number ranges are included in this recall. Product Name Item Code Product Description Serial Number Range Start Serial Number Range End Date of Manufacture Prestige Solo - PA PA110 Prestige Solo PA Series PA044936 PA147874 PA155 Prestige Solo PA Series PA045337 PA147522 PA175 Prestige Solo PA Series PA044728 PA148532 PA250 Prestige Solo PA Series PA044768 PA149487 PA299 Prestige Solo PA Series PA045398 PA146746 PA399 Prestige Solo PA Series PA045420 PA148752 PA80 Prestige Solo PA Series PA044058 PA139939 Dec 2015 - Apr 2019 Prestige Solo PT PT110 Prestige Solo PT Series PT0000110 PT0053558 PT110 Prestige Solo PT Series PTA002845 PTA037637 PT110LP Prestige Solo PT Series PT0000928 PT0053557 PT110LP Prestige Solo PT Series PTA002645 PTA002764 PT175 Prestige Solo PT Series PT0002849 PT0053776 PT175 Prestige Solo PT Series PTA003087 PTA037557 PT250 Prestige Solo PT Series PT0002588 PT0053319 PT250 Prestige Solo PT Series PTA003207 PTA037467 PT399 Prestige Solo PT Series PT0005962 PT0052417 PT399 Prestige Solo PT Series PTA003388 PTA037377 PT399HP Prestige Solo PT Series PT0010893 PT0052394 PT399HP Prestige Solo PT Series PTA003496 PTA097961 PT60 Prestige Solo PT Series PT0002188 PT0051954 PT60 Prestige Solo PT Series PTA002810 PTA008253 Dec 2011 - Dec 2015 Prestige Excellence - PTE PTE110LP Prestige Excellence PT PT0001588 PT0053690 PTE110LP Prestige Excellence PTE PTE030446 PTE030479 PTE110 Prestige Excellence PT000568 PT0053624 PTE110 Prestige Excellence PTEA PTA002889 PTA003086 PTE110 Prestige Excellence PTE PTE049177 PTE049177 Dec 2011 - Dec 2015 Prestige Excellence - PEA PEA110 Prestige Excellence PEA PEA078169 PEA143958 Dec 2015 - Apr 2019 Aerco Esteem PT399ES Aerco Esteem AE1100 AE1236 PT399HP Aerco Esteem AE1237 AE1239 DF48650G/BK/P DF48650G/BK/P/LP DF48650G/S/P Dec 2011 - Dec 2015
This recall involves all Canyon Speedmax CF triathlon bicycle models R073 and R41 with V21 aerostems. The carbon fiber bikes were sold in black/red, black/blue, gray/orange, and red and black. "Canyon" is printed on the downtube. "Speedmax" is printed on the top tube. "V21" is printed on the left side of the stem. The model number can be found on a sticker at the top of the seat tube, just below the saddle.
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.
Undeclared Red #3
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.