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. 2,862 recalls have been distributed to Texas in the last 12 months.
Showing 7881–7900 of 30,921 recalls
Recalled Item: Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter...
The Issue: Product may not be sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 630G/ MMT-1715 Recalled by Medtronic MiniMed Due...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simple Clamp Recalled by Baxter Healthcare Corporation Due to the adhesive,...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allen Standard Starburst Recalled by Baxter Healthcare Corporation Due to...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allen Advance Table Recalled by Baxter Healthcare Corporation Due to the...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allen Life Assist Beach Chair Recalled by Baxter Healthcare Corporation Due...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Flex Polar Head Positnr-Device Only Recalled by Baxter Healthcare...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beach Chair Clamp Recalled by Baxter Healthcare Corporation Due to the...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X (IS4200) and Xi (IS4000) systems Recalled by Intuitive Surgical,...
The Issue: Inadvertent energy delivery from surgical system instrument if 1) Force...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MP Port Titanium Low Profile Implanted Port with 5F Recalled by...
The Issue: Printed Instructions for Use (IFU) not shipped with device. The Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has become aware of three potential software issues with ARTIS pheno...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 125 series iGO2 Portable Oxygen Concentrator-indicated for the...
The Issue: An unapproved adhesive used to manufacture the accumulator tank sub assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium (Li) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP software of the Ivenix Infusion System (IIS) Recalled by Fresenius Kabi...
The Issue: Retroactively reported correction from 2022: A software defect may cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prep-Fill Guarded Luer Connector (GLC): a. Part Number 57-400 Recalled by...
The Issue: Blister package had an unsealed edge compromising sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berkeley VC-10 Vacuum Curettage System Recalled by Olympus Corporation of...
The Issue: Update to the Instruction for Use (IFU): Olympus is adding a new warning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B. Braun CARESITE Port Access Kit w/Tegaderm Recalled by Medical Action...
The Issue: The kits were incorrectly labeled with an extended expiration date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESITE SMALLBORE EXT SET T-PORT 5 IN. Recalled by B. Braun Medical, Inc....
The Issue: The extension set has a high probability of potential failure which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTRASITE US04TL Smallbore T-Port Extension Set Recalled by B. Braun...
The Issue: The extension set has a high probability of failure which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.