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. 2,048 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,048 in last 12 months

Showing 2560125620 of 55,713 recalls

DrugNovember 27, 2018· Teva Pharmaceuticals USA

Recalled Item: Amlodipine Recalled by Teva Pharmaceuticals USA Due to CGMP Deviations: FDA...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 27, 2018· Sprout Creek Farm, Inc.

Recalled Item: Sprout Creek Farm Kinkead raw cows' milk cheese semi-firm savory Recalled by...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 27, 2018· Gemini Food Corporation Inc

Recalled Item: Imperial Taste Fried Garlic Recalled by Gemini Food Corporation Inc Due to...

The Issue: Investigation of consumer complaint found that two products had undeclared...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 27, 2018· Gemini Food Corporation Inc

Recalled Item: Imperial Taste Fried Red Onion Recalled by Gemini Food Corporation Inc Due...

The Issue: Investigation of consumer complaint found that two products had undeclared...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 27, 2018· ICU Medical, Inc.

Recalled Item: ICU Medical Recalled by ICU Medical, Inc. Due to Reports of pressure tubing...

The Issue: Reports of pressure tubing separation between the sampling port and the high...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· ICU Medical, Inc.

Recalled Item: ICU Medical Recalled by ICU Medical, Inc. Due to Reports of pressure tubing...

The Issue: Reports of pressure tubing separation between the sampling port and the high...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· ICU Medical, Inc.

Recalled Item: ICU Medical Recalled by ICU Medical, Inc. Due to Reports of pressure tubing...

The Issue: Reports of pressure tubing separation between the sampling port and the high...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· Medtronic Perfusion Systems

Recalled Item: RESERVOIR "Y" ADAPTER Recalled by Medtronic Perfusion Systems Due to...

The Issue: Medtronic discovered that certain Y-connectors included in the suction lines...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· Medtronic Perfusion Systems

Recalled Item: SUCTION / ANTICOAGULATION ASSEMBLY (a) BTC93 (b) BTC98 Suction and Recalled...

The Issue: Medtronic discovered that certain Y-connectors included in the suction lines...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· AROA BIOSURGERY

Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...

The Issue: Potential for pouch seal failure

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· AROA BIOSURGERY

Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...

The Issue: Potential for pouch seal failure

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· AROA BIOSURGERY

Recalled Item: Endoform Dermal Template 4x5 Recalled by AROA BIOSURGERY Due to Potential...

The Issue: Potential for pouch seal failure

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2018· Tris Pharma Inc.

Recalled Item: infants* IBUPROFEN Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 26, 2018· Tris Pharma Inc.

Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 26, 2018· Tris Pharma Inc.

Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 26, 2018· Smiths Medical ASD Inc.

Recalled Item: ProtectIV¿ Plus Safety IV Catheter Recalled by Smiths Medical ASD Inc. Due...

The Issue: Certain lots of the Model 306701 ProtectIV¿ Plus Safety IV Catheter may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2018· Philips North America LLC

Recalled Item: HeartStart MRx Recalled by Philips North America LLC Due to Affected...

The Issue: Affected lithium-ion batteries may contain a defective component (Thermal...

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

Class II — Potential Health HazardOngoing
FoodNovember 21, 2018· Ottogi America Inc

Recalled Item: Ottogi Jin Ramen Mild NET WT. 1lb 5.16oz Recalled by Ottogi America Inc Due...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 21, 2018· Ottogi America Inc

Recalled Item: Ottogi Jin Ramen Spicy NET WT. 1lb 5.16oz Recalled by Ottogi America Inc Due...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 21, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to Due...

The Issue: Due to a manufacturing variation in the arm that can result in a persistent...

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

Class II — Potential Health HazardOngoing