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. 2,587 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,587 in last 12 months

Showing 39814000 of 30,921 recalls

Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim 5 Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Proclaim 5 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim 7 Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim XR 7 Implantable Pulse Generator Recalled by Abbott Medical...

The Issue: The duration between the implantable pulse generator reaching the elective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim Plus 7 Implantable Pulse Generator Recalled by Abbott...

The Issue: The duration between the implantable pulse generator reaching the elective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim Plus 5 Implantable Pulse Generator Recalled by Abbott...

The Issue: The duration between the implantable pulse generator reaching the elective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: US AquaA 900H-Typ USA-3 x 208v-Intended for the purification of Recalled by...

The Issue: Concentrate Flow was exceeding the maximum 19.9 bar set point. The standard...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim DRG Implantable Pulse Generator Recalled by Abbott Medical...

The Issue: The duration between the implantable pulse generator reaching the elective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim Plus 5 Implantable Pulse Generator Recalled by Abbott...

The Issue: The duration between the implantable pulse generator reaching the elective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim 5 Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Proclaim 7 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Medtronic Perfusion Systems

Recalled Item: TourniKwik Tourniquet Set (CFN 79012) Recalled by Medtronic Perfusion...

The Issue: Incorrect component placed in four manufactured lots of the TourniKwik"...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: ACL Recalled by American Contract Systems Inc Due to Ethylene Oxide/Ethylene...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: HAND WRIST FOREARM-LF Procedure tray Catalog Number: CCHD17B Recalled by...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: HAND DRAPING SJH-Procedure Kit Catalog Number: SJHD67F Recalled by American...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: HAND PACK-Procedure Kit Catalog Number: WEHD16B Recalled by American...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: UPPER EXTREMITY PK Recalled by American Contract Systems Inc Due to Ethylene...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: TOTAL KNEE - 247546 - Procedure tray Catalog Number: BFTK01AA Recalled by...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· Hamilton Medical AG

Recalled Item: Ventilator HAMILTON-C6 Recalled by Hamilton Medical AG Due to Ventilator may...

The Issue: Ventilator may enter sensor fail mode, ventilation may not re-initiate,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: TOTAL KNEE -Procedure Kit Catalog Number: QPTK95A Recalled by American...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing