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. 2,697 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,697 in last 12 months

Showing 2266122680 of 55,713 recalls

Medical DeviceAugust 1, 2019· Stryker Communications

Recalled Item: Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel Recalled...

The Issue: The mounts on the monitor may have an insufficient weld.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2019· Aerolase Corporation

Recalled Item: LightPod Neo Lasers Recalled by Aerolase Corporation Due to This relates to...

The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder...

The Issue: Separation of front and rear barrels upon activation of the safety feature...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The injector holder could potentially fall off together with the injector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Stryker Instruments Div. of Stryker Corporation

Recalled Item: C2 Nerve Monitor Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Stryker C2 NerveMonitor's design and instructions may not optimally address...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2019· Stryker Instruments Div. of Stryker Corporation

Recalled Item: C2 Nerve Monitor Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Stryker C2 NerveMonitor's design and instructions may not optimally address...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan Uncuffed: a) 2.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Atellica CH 930 Analyzer. Siemens Material Number (SMN): 11067000...

The Issue: Atellica CH 930 Analyzer - Erroneous Indices for Hemolysis and Lipemia in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System...

The Issue: Artis zee/Q systems patient tables may potentially have cracks in the table...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Sheridan/CF Novaplus 7.0 mm Recalled by Teleflex Medical Due to Reported...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan LTS: a) 4.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan/HVT: a) 5.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Sheridan/HVT Novaplus: a) 7.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing