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 39013920 of 30,921 recalls

Medical DeviceJune 3, 2024· Microtek Medical Inc.

Recalled Item: Bottle Decanter Recalled by Microtek Medical Inc. Due to During sterile...

The Issue: During sterile barrier testing performed on the decanter product line, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: RTL190904: 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Microtek Medical Inc.

Recalled Item: C-Flow Bag Decanter Recalled by Microtek Medical Inc. Due to During sterile...

The Issue: During sterile barrier testing performed on the decanter product line, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Microtek Medical Inc.

Recalled Item: Transfer Device Recalled by Microtek Medical Inc. Due to During sterile...

The Issue: During sterile barrier testing performed on the decanter product line, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Qiagen Sciences LLC

Recalled Item: QIAcube Connect MDx - IVD Instrument designed to perform automated Recalled...

The Issue: Heater shaker module does not perform heating if the temperature is set...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: RTL190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings,...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: RTLR190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings,...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings, Inc....

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2024· Treace Medical Concepts, Inc.

Recalled Item: Nanoplasty 3D Bunion Correction System Implant Recalled by Treace Medical...

The Issue: Potential issue causing a higher frequency of interference with locking...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Avanos Medical, Inc.

Recalled Item: MIC-KEY* Gastric-Jejunal Feeding Tube Kit Recalled by Avanos Medical, Inc....

The Issue: The IFU was missing some risk information requested by another country to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MP - Inended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Abiomed, Inc.

Recalled Item: Impella CP with SmartAssist Recalled by Abiomed, Inc. Due to Nine (9)...

The Issue: Nine (9) Impella CP pumps failed inspection and were inadvertently released.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 31, 2024· Stryker Sustainability Solutions

Recalled Item: Recalled by Stryker Sustainability Solutions Due to Mislabeling

The Issue: Mislabeling; tourniquet cuff packaging labeled as dual port single bladder...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Vertix Solitaire - The Vertix MD Trauma has been Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MP - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for...

The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...

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

Class II — Potential Health HazardOngoing