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. 2,680 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,680 in last 12 months

Showing 2734127360 of 30,921 recalls

Medical DeviceNovember 25, 2013· Elekta, Inc.

Recalled Item: XiO RTP System The XiO RTP System is used to Recalled by Elekta, Inc. Due to...

The Issue: When the number of fractions is changed for a proton spot beam, the MU are...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2013· Carestream Health, Inc.

Recalled Item: DR 7500 with FF WS These products are permanently installed Recalled by...

The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2013· Carestream Health, Inc.

Recalled Item: DRX-Evolution with CSH WS These products are permanently installed...

The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2013· Elekta, Inc.

Recalled Item: Synergy XVI The Elekta Synergy S is intended to be Recalled by Elekta, Inc....

The Issue: Potential collision risk when using XVI and external beam shaping devices.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2013· Elekta, Inc.

Recalled Item: Synergy XVI XVI can incorrectly calculate the target position of Recalled by...

The Issue: XVI can incorrectly calculate the target position of the treatment table.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2013· Navilyst Medical, Inc.

Recalled Item: Port Kit with Access Infusion Set under the following labels: Recalled by...

The Issue: Navilyst Medical has recalled a Port Kit with Access Infusion Set due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2013· Elekta, Inc.

Recalled Item: XiO RTP System. Used to create treatment plans for any Recalled by Elekta,...

The Issue: When bolus is present, the Effective Depth (with bolus) to the weight point...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2013· Elekta, Inc.

Recalled Item: RT Desktop The EOS RT Desktop Recalled by Elekta, Inc. Due to During the...

The Issue: During the treatment table, gantry, and collimator calibration procedures,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2013· Abbott Molecular

Recalled Item: The Abbott m2000sp is an automated system for performing sample Recalled by...

The Issue: The x-drive assembly may fail prematurely. This could cause the manipulator...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1762: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043W-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4040-2: Umbilical 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1469J: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1725: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4042E: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Bio-Rad Laboratories, Inc.

Recalled Item: D-10 Dual Program Recalled by Bio-Rad Laboratories, Inc. Due to D-10 A1c...

The Issue: D-10 A1c Dual Program Floppy was programmed incorrectly and cartridge...

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

Class III — Low RiskOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043E: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4042LH: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion...

The Issue: Smiths Medical is conducting a recall involving all Medfusion¿ 4000 Syringe...

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

Class II — Potential Health HazardOngoing