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. 2,677 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,677 in last 12 months

Showing 3170131720 of 55,713 recalls

Medical DeviceJune 1, 2017· Solta Medical Inc

Recalled Item: VASER Amplifier Recalled by Solta Medical Inc Due to Potential inaccurate...

The Issue: Potential inaccurate calibration by service depot repair, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Solta Medical Inc

Recalled Item: VASER PRO Amplifier Recalled by Solta Medical Inc Due to Potential...

The Issue: Potential inaccurate calibration by service depot repair, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 2000 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 1000 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Product Usage: The da Vinci Recalled by...

The Issue: da Vinci Xi(R) Surgical System Patient Side Carts (PSC) were shipped to the...

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

Class II — Potential Health HazardOngoing
DrugMay 31, 2017· Teva Pharmaceuticals

Recalled Item: Paliperidone Extended-Release Tablets Recalled by Teva Pharmaceuticals Due...

The Issue: Failed Dissolution Specifications: Drug release test result, obtained during...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodMay 31, 2017· Blue Diamond Growers

Recalled Item: Blue Diamond Almonds Blanc DCD FN C (blanched diced fine) Recalled by Blue...

The Issue: Firm was notified by customer of a positive Salmonella result obtained when...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 31, 2017· Becton Dickinson & Company

Recalled Item: BD Precision Glide Needle 18G x 1 RB Recalled by Becton Dickinson & Company...

The Issue: Hub damage resulting in breakage and/or leakage during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2017· Soft Computer Consultants, Inc.

Recalled Item: SoftLab Software Laboratory information system to be used in a Recalled by...

The Issue: Display of lab results based on incorrect LOINC code/test descriptions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2017· Encore Medical, Lp

Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...

The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2017· Encore Medical, Lp

Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...

The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...

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

Class II — Potential Health HazardOngoing
DrugMay 30, 2017· Mckesson Packaging Services

Recalled Item: BuPROPion HCL Tablets Recalled by Mckesson Packaging Services Due to Failed...

The Issue: Failed Moisture Limits: Product tested out-of-specification for moisture...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 18 cm (7") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold Recalled by...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 10" Smallbore Ext Set w/6-Port NanoClave¿ Manifold (Orange Recalled by ICU...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 10" Smallbore Ext Set w/6-Port NanoClave¿ Manifold Recalled by ICU Medical,...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 168 cm (66") Appx 2.6 ml Recalled by ICU Medical, Inc. Due to The connection...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 28 cm (11") PUR Bifuse Ext Set w/6-Port NanoClave¿ Manifold Recalled by ICU...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 28 cm (11") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold Recalled by...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 10" Smallbore Ext Set w/6-Port NanoClave¿ Manifold (Orange Recalled by ICU...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: PROXIMALE - 28 cm (11") Smallbore Ext Set w/6-Port NanoClave¿ Manifold...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing