Product Recalls in Texas
Product recalls affecting Texas — including food, drugs, consumer products, medical devices, and vehicles distributed to Texas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,680 recalls have been distributed to Texas in the last 12 months.
Showing 24841–24860 of 30,921 recalls
Recalled Item: Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...
The Issue: Power supply malfunction complaints related to suboptimal thermal management.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Proteus XR/a with wall stand model number 2260354. Recalled by...
The Issue: Potential breakage of the steel cable which supports the bucky device in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1...
The Issue: If the patient sits on either wing, not squarely on the center section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Precise Treatment Table Recalled by Elekta, Inc. Due to It is...
The Issue: It is possible to position the Treatment Table with errors greater than 5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis Recalled...
The Issue: An increase in complaints of loosening and radiolucent lines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9F Plastic Dual Port Recalled by Medical Components, Inc dba MedComp Due to...
The Issue: The dual port with catheters was not covered under FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Engstrom Carestation Recalled by GE Healthcare Due to...
The Issue: Potential failure of the caster mounting hardware, which may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...
The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...
The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...
The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisher Brand Gel Infant Heel Gel Warmers Recalled by CooperSurgical, Inc....
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice WarmGel Infant Heel Warmer Recalled by CooperSurgical, Inc. Due...
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Brand Warm Gel Infant Heel Gel Warmer Recalled by CooperSurgical,...
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical Infant Heel Gel Warmers Recalled by CooperSurgical, Inc. Due...
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-PLASTY Cannula (Needle) Recalled by Biologic Therapies, Inc Due to...
The Issue: Devices are misbranded - failure to properly classify and obtain FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Passport V Monitor Recalled by Mindray DS USA, Inc. dba Mindray North...
The Issue: An issue has been identified with Passport V Monitors invasive blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-CORE Cannula (Needle) Set Recalled by Biologic Therapies, Inc Due to...
The Issue: Devices are misbranded - failure to properly classify and obtain FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-MAC Cannula (Needle) Set Recalled by Biologic Therapies, Inc Due to...
The Issue: Devices are misbranded - failure to properly classify and obtain FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAX-TL 9.0 x 7.0 mm Implant Recalled by Southern Implants, Inc Due to Z-MAX...
The Issue: Z-MAX Implant, 9mm diameter, 7mm length labeled package, catalog number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORUM Archive and Viewer Recalled by Carl Zeiss Meditec AG Due to Software...
The Issue: Software defect in the FORUM Viewer versions 3.1 and 3.2 which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.