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. 896 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
896 in last 12 months

Showing 54261–54280 of 55,713 recalls

Medical DeviceJuly 13, 2012· Hospira Inc.

Recalled Item: Hospira LifeShield Latex-Free 100 mL Burette Set Recalled by Hospira Inc....

The Issue: The float valve in the burette sticks to the burette wall and does not open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2012· Westone Laboratories, Inc.

Recalled Item: Oto Ease by Westone Recalled by Westone Laboratories, Inc. Due to Westone is...

The Issue: Westone is recalling all Oto Ease ear lubricant in all packaging...

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

Class II — Potential Health HazardOngoing
FoodJuly 13, 2012· Southern Bakeries, LLC

Recalled Item: Nature's Grain Garlic French Bread Recalled by Southern Bakeries, LLC Due to...

The Issue: Southern Bakeries, Hope, AR is recalling its Nature's Grain Garlic French...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Hot Salsa Recalled by Pulmuone...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Organic Medium Salsa Recalled by Pulmuone Wildwood Inc Due to The...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Medium Salsa - Canada (containing...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Mild Salsa Recalled by Pulmuone...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Organic Mild Salsa Recalled by Pulmuone Wildwood Inc Due to The...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Medium Salsa Recalled by Pulmuone...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Mild Salsa - Canada (containing...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 12, 2012· Alere San Diego, Inc.

Recalled Item: Alere Triage TOX Drug Screen 9 Panel Recalled by Alere San Diego, Inc. Due...

The Issue: Alere San Diego is recalling Alere Triage TOX Drug Screen because there is a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2012· Aesculap Implant Systems LLC

Recalled Item: Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD Recalled...

The Issue: The 4 degree and 9 degree trial instruments (SJ768T-US/SJ780T-US) are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a number of potential issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: V*Care Resuscitator Infant Resuscitator Recalled by Ventlab Corporation Due...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Straumann USA, LLC

Recalled Item: Straumann Narrow CrossFit (NC) Screw for CARES Abutment ZrO2. Endosseous...

The Issue: Incorrect Screw (RC) included with NC CARES Abutment Set was not a Narrow...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: Safe Spot Infant Resuscitator Recalled by Ventlab Corporation Due to...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: AirFlow Resuscitator Recalled by Ventlab Corporation Due to Possible volume...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing