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. 2,905 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,905 in last 12 months

Showing 32013220 of 55,713 recalls

FoodFebruary 27, 2025· Uncle Rays, LLC

Recalled Item: Coyote Valley Sour Cream & Onion Chips Recalled by Uncle Rays, LLC Due to...

The Issue: Product contains higher sodium amount than stated on label

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 27, 2025· Amgen, Inc.

Recalled Item: Neupogen (filgrastim) For Injection Recalled by Amgen, Inc. Due to Stability...

The Issue: Stability data does not support expiry: the products have the potential to...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 27, 2025· Amgen, Inc.

Recalled Item: Neupogen (filgrastim) For Injection Recalled by Amgen, Inc. Due to Stability...

The Issue: Stability data does not support expiry: the products have the potential to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2025· Tandem Diabetes Care, Inc.

Recalled Item: t:slim X2 Insulin Pump with Interoperable Technology Recalled by Tandem...

The Issue: A software defect in Version 7.9 of the pump software for Tandem t:slim X2...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 27, 2025· Tandem Diabetes Care, Inc.

Recalled Item: Tandem Mobi Insulin Pump with Interoperable Technology Recalled by Tandem...

The Issue: A software defect in Version 7.9 of the pump software for Tandem t:slim X2...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 27, 2025· Premier Dental Products Co

Recalled Item: Premier Solo Diamond - Large Invented Cone Recalled by Premier Dental...

The Issue: The hardness not meeting the material specification and may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2025· Zimmer, Inc.

Recalled Item: NexGen LPS Flex Recalled by Zimmer, Inc. Due to The "Use with plate 7, 8, 9,...

The Issue: The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label...

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

Class II — Potential Health HazardOngoing
FoodFebruary 26, 2025· Paletas Ice Cream, LLC

Recalled Item: Flor de Michoacan Blue Hawaiian Artificially Flavored Beverage Concentrate....

The Issue: Undeclared Red #3

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 26, 2025· Qapel Medical Inc.

Recalled Item: Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration...

The Issue: Aspiration catheter distal tip features and characteristics may not be in...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 26, 2025· Beckman Coulter Inc.

Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...

The Issue: Beckman Coulter has determined that device software versions V1.3, V1.4,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2025· Intuitive Surgical, Inc.

Recalled Item: Brand Name: Da Vinci 5 Product Name: ASSY Recalled by Intuitive Surgical,...

The Issue: Due to an increase in complaints concerning foot tray pedal spring failing...

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

Class II — Potential Health HazardOngoing
DrugFebruary 25, 2025· A-S Medication Solutions LLC

Recalled Item: METFORMIN HYDROCHLORIDE EXTENDED- RELEASE 500MG Recalled by A-S Medication...

The Issue: Presence of Foreign Tablets/Capsules.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2025· MYLAN PHARMACEUTICALS INC

Recalled Item: Prasugrel Tablets Recalled by MYLAN PHARMACEUTICALS INC Due to Failed...

The Issue: Failed Dissolution Specifications - low dissolution results

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Otopore Cylinder outer ear wound dressing Recalled by Stryker Corporation...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore FD fragmentable nasal dressing Recalled by Stryker Corporation Due...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Otopore Square outer ear wound dressing Recalled by Stryker Corporation Due...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Hemopore 8cm nasal/sinus temporary wound dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Hemopore 2PK nasal/sinus temporary wound dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore Standard 8cm fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 4cm Standard 2PK fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing