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 17411760 of 55,713 recalls

Medical DeviceAugust 18, 2025· Boston Scientific Corporation

Recalled Item: Preventive Maintenance (PM) Kit ICEFX Recalled by Boston Scientific...

The Issue: Certain desiccant tube subassemblies were built with end caps that were not...

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

Class II — Potential Health HazardOngoing
FoodAugust 16, 2025· TAMPA MAID FOODS, LLC

Recalled Item: Clean-tail Coconut Farm Raise Breaded Butterfly Shrimp Clean Tail (21/25...

The Issue: Product may be contaminated with Cesium-137 (Cs-137)

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 16, 2025· TAMPA MAID FOODS, LLC

Recalled Item: ADMIRAL OF THE FLEET and PORTICO SEAFOOD CLASSIC (SYSCO) Cleantail Recalled...

The Issue: Product may be contaminated with Cesium-137 (Cs-137)

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 16, 2025· TAMPA MAID FOODS, LLC

Recalled Item: Panko Style Breaded Butterfly Shrimp (16/20 CT per pound) in bulk packaging...

The Issue: Product may be contaminated with Cesium-137 (Cs-137)

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 15, 2025· Anderson Candy Company, LLC

Recalled Item: Peanut rounds 2.25 oz and 3 oz Recalled by Anderson Candy Company, LLC Due...

The Issue: Undeclared soy allergen

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 15, 2025· Maquet Cardiovascular, LLC

Recalled Item: Heartstring III Proximal Seal System. Intravascular anastomosis occluder....

The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017 Recalled by...

The Issue: Potential for activation of an abnormal alarm pause.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· ETHICON, LLC

Recalled Item: STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device...

The Issue: Potential for barb non-engagement.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Exactech, Inc.

Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...

The Issue: Reverse Shoulder humeral liners have an articular surface position outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Maquet Cardiovascular, LLC

Recalled Item: Heartstring III Proximal Seal System Recalled by Maquet Cardiovascular, LLC...

The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Exactech, Inc.

Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...

The Issue: Reverse Shoulder humeral liners have an articular surface position outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Maquet Cardiovascular, LLC

Recalled Item: Heartstring III Proximal Seal System Recalled by Maquet Cardiovascular, LLC...

The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...

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

Class II — Potential Health HazardOngoing
FoodAugust 14, 2025· Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Recalled Item: Frozen AquaStar Breaded Shrimp Recalled by Admiralty Island Fisheries Inc...

The Issue: Product may be contaminated with Cesium-137 (Cs-137).

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 14, 2025· Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Recalled Item: Frozen Mercado Kroger Cooked Shrimp - Medium - Peeled - Recalled by...

The Issue: Product may be contaminated with Cesium-137 (Cs-137).

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 14, 2025· Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Recalled Item: AquaStar Cocktail Shrimp Recalled by Admiralty Island Fisheries Inc dba...

The Issue: Product may be contaminated with Cesium-137 (Cs-137).

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing