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. 2,581 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,581 in last 12 months

Showing 5546155480 of 55,713 recalls

FoodMay 31, 2011· Wynlife Healthcare, Inc.

Recalled Item: Vegi-Fiber Plus Recalled by Wynlife Healthcare, Inc. Due to Wynlife...

The Issue: Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 31, 2011· Wynlife Healthcare, Inc.

Recalled Item: All-In-One Probiotics Recalled by Wynlife Healthcare, Inc. Due to Wynlife...

The Issue: Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 31, 2011· BioDerm, Inc.

Recalled Item: BioDerm Liberty Pouch Clean & Dry External Male Catheter Specialty Recalled...

The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component skin...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2011· BioDerm, Inc.

Recalled Item: BioDerm Safe n' Dry 21006 (Component: SKIN-PREP Protective wipes). The...

The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component (Smith...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2011· BioDerm, Inc.

Recalled Item: BioDerm Liberty 3.0 External Male Catheter Specialty Type with integral...

The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component skin...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2011· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: Varian High Energy Clinacs Recalled by Varian Medical Systems, Inc. Oncology...

The Issue: Under certain conditions, photon beams in High Energy Clinacs may experience...

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

Class II — Potential Health HazardOngoing
DrugMay 27, 2011· A B Nutrition, Inc.

Recalled Item: PIRACETAM COGNITION ENHANCING AGENT Dietary Supplement PHARMACEUTICAL GRADE...

The Issue: Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 27, 2011· A B Nutrition, Inc.

Recalled Item: PIRACETAM POWDER COGNITION ENHANCING AGENT Dietary Supplement CTD 500 grams...

The Issue: Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 27, 2011· A B Nutrition, Inc.

Recalled Item: ANIRACETAM FAST ACTING NOOTROPIC Dietary Supplement PHARMACEUTICAL GRADE...

The Issue: Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 24, 2011· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune¿ 2 Rover - ULTRA ~120V ~ 60 Hz 12A Recalled by Stryker Instruments...

The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2011· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune¿ 2 Rover - ULTRA ~230V ~ 50 Hz 12A Recalled by Stryker Instruments...

The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2011· Linvatec Corp. dba ConMed Linvatec

Recalled Item: ******Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source Recalled by...

The Issue: Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2011· Linvatec Corp. dba ConMed Linvatec

Recalled Item: ******Qty 1*** EC REP*** ConMed Linvatec Xenon Universal Light Source...

The Issue: Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2011· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: DPM Central Station Mindray DS USA Recalled by Mindray DS USA, Inc. d.b.a....

The Issue: There is a software anomaly with the DPM Central Monitoring System where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2011· The Anspach Effort, Inc.

Recalled Item: Product Catalog (part number 20-0020) utilized with the Electric and...

The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2011· The Anspach Effort, Inc.

Recalled Item: Cutting Bur Chart (part number 20-0019) utilized with the Electric Recalled...

The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2011· The Anspach Effort, Inc.

Recalled Item: Pneumatic Systems Operating Manual (part numbers 19-0005) utilized with the...

The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...

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

Class II — Potential Health HazardOngoing
FoodMay 2, 2011· Mothers' Milk Bank at Austin

Recalled Item: Mother's Milk Bank at Austin Recalled by Mothers' Milk Bank at Austin Due to...

The Issue: The product had the potential to contain foreign materials.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 2, 2011· Mothers' Milk Bank at Austin

Recalled Item: Mother's Milk Bank at Austin Recalled by Mothers' Milk Bank at Austin Due to...

The Issue: The product had the potential to contain foreign materials.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 2, 2011· BRAEMAR, INC.

Recalled Item: Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-00...

The Issue: Braemar Inc., became aware of a battery related incident that occurred with...

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

Class II — Potential Health HazardOngoing