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. 2,692 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,692 in last 12 months

Showing 2512125140 of 55,713 recalls

FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Beijing Spicy Seafood Noodle 5PK 1lb 5.16oz x 8pk Recalled by Ottogi...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Jjajang Bokki (Bowl) 4.23oz x 12ea Item #21502157 Manufactured...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Ppushu Ppushu Grilled Chicken Flavor 3.17oz x 40ea Item Recalled by...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Ppushu Ppushu Spicy Flavor 3.17oz x 40ea Item #21503008 Recalled by...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Ramen Bokki (Cup) 4.23oz x 12ea Item #21309009 Manufactured Recalled...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Beijing JJajang Noodle 5PK 1lb 7.81oz x 8pk Item Recalled by Ottogi...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Spicy Seafood Flavor Udon Odongtong (Bowl) 3.53oz x 12ea Recalled by...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Snack Ramen 5PK Recalled by Ottogi America Inc Due to Undeclared Allergen

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2019· Ottogi America Inc

Recalled Item: Ottogi Yeul Ramen (Bowl) 4.06oz x 12ea Item #21305007 Manufactured Recalled...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 15, 2019· 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
DrugJanuary 15, 2019· 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
DrugJanuary 15, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Ezetimibe and Simvastatin Tablets 10mg/80 mg Recalled by Dr. Reddy's...

The Issue: Presence of Foreign Substance: Product complaint of black speckles observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2019· Advanced Pharma Inc.

Recalled Item: HEPERAIN 50 mg/50 mL (1mg/mL) Injectable Solution Recalled by Advanced...

The Issue: Labeling; Label Error on Declared Strength; label incorrectly states the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2019· 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
DrugJanuary 15, 2019· LUPIN SOMERSET

Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by LUPIN SOMERSET Due to...

The Issue: Failed Impurities/Degradation Specifications: Expansion of October 2018...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 15, 2019· Westmed, Inc.

Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit With Neonatal Mask Recalled by...

The Issue: A repair was made to an adapter mold resulting in parts being produced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2019· Westmed, Inc.

Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit With Infant Mask Recalled by...

The Issue: A repair was made to an adapter mold resulting in parts being produced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2019· Westmed, Inc.

Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit Recalled by Westmed, Inc. Due...

The Issue: A repair was made to an adapter mold resulting in parts being produced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2019· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm FDR Go PLUS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...

The Issue: FUJIFILM Medical Systems U.S.A., Inc., Modality Systems became aware of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2019· Miami Device Solutions, LLC.

Recalled Item: Proximal Humerus Plate Recalled by Miami Device Solutions, LLC. Due to Right...

The Issue: Right Proximal Humerus Plates. Product component parts MDS130108R, may be...

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

Class II — Potential Health HazardOngoing