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. 1,136 recalls have been distributed to Texas in the last 12 months.
Showing 14101–14120 of 30,921 recalls
Recalled Item: SOMATOM Drive Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAsymphony SP SOW 5.0.3 Recalled by Qiagen Sciences LLC Due to QIAsymphony...
The Issue: QIAsymphony software version 5.0.3 - Software issue incorreclty assigns the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151813 Recalled by...
The Issue: Cleaning processes potentially being ineffective
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric...
The Issue: The firm conducted internal investigations that confirmed customer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151815 Recalled by...
The Issue: Cleaning processes potentially being ineffective
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810 Recalled by...
The Issue: Cleaning processes potentially being ineffective
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151814 Recalled by...
The Issue: Cleaning processes potentially being ineffective
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151811 Recalled by...
The Issue: Cleaning processes potentially being ineffective
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812 Recalled by...
The Issue: Cleaning processes potentially being ineffective
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blanketrol II Hyper-Hypothermia System Recalled by Cincinnati Sub-Zero...
The Issue: Warnings statements have been added- exceeding 40 degree C for extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blanketrol III Hyper-Hypothermia System- body hypothermia system temperature...
The Issue: Warnings statements have been added- exceeding 40 degree C for extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoolBlue Hyper-Hypothermia System- body hypothermia system Model: Innercool...
The Issue: Warnings statements have been added- exceeding 40 degree C for extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIRCUMCISION TRAY Kit Code: CIT2245 - Product Usage: Kit is Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAILY DRIVELINE KIT Kit Code: DM940 - Product Usage: Kit Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Erisma- LP posterior fixation system with the below specifically affected...
The Issue: Potential for the polyaxial screw to become disassembled during implant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris EtCO2 Recalled by CareFusion 303, Inc. Due to Calibration; it has...
The Issue: Calibration; it has been determined that the capnographs may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRIVELINE MANAGEMENT TRAY Kit Code: DT17780B - Product Usage: Kit Recalled...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIRCUMCISION TRAY Kit Code: CIT2650H - Product Usage: Kit is Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE FLUORO SSP TRAY Kit Code: MNS11605 - Product Usage: Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.