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 23412360 of 55,713 recalls

DrugJune 19, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Defective...

The Issue: Defective container; blister packaging inadequately sealed.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Defective...

The Issue: Defective container; blister packaging inadequately sealed.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2025· Professional Botanicals, Inc.

Recalled Item: Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable...

The Issue: Products contains Magnesium Salicylate.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2025· Professional Botanicals, Inc.

Recalled Item: Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable...

The Issue: Products contains Magnesium Salicylate.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2025· Professional Botanicals, Inc.

Recalled Item: Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule....

The Issue: Products contains Magnesium Salicylate.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2025· Krasnyi Oktyabr USA Inc

Recalled Item: ARAL FISH Recalled by Krasnyi Oktyabr USA Inc Due to Clostridium botulinum...

The Issue: Clostridium botulinum (uneviscerated fish)

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 18, 2025· Prestige Brands Holdings

Recalled Item: Little Remedies¿ Honey Cough 4 FL OZ (118 mL) Recalled by Prestige Brands...

The Issue: contaminated with Bacillus cereus and may be spoiled

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2025· Lipari Foods Operating Company, LLC.

Recalled Item: JLM Manufacturing Dark Chocolate Nonpareils Recalled by Lipari Foods...

The Issue: Undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 18, 2025· C.R. Bard Inc

Recalled Item: Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated...

The Issue: Foley catheter may have an obstructed lumen, which may result in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Osteotec Limited

Recalled Item: Brand Name: Osteotec Product Name: Osteotec Silicone Finger Implant...

The Issue: There is the potential that the silicone implant may contain foreign material

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Medtronic, Inc.

Recalled Item: Medtronic CareLink SmartSync Patient Connector Recalled by Medtronic, Inc....

The Issue: In prior SmartSync application versions, the Abort button stopped the test...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Stryker Corporation

Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...

The Issue: Due to complaints their is the potential that irrigation solution may leaked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Medtronic, Inc.

Recalled Item: Medtronic CareLink SmartSync Device Manager Recalled by Medtronic, Inc. Due...

The Issue: In prior SmartSync application versions, the Abort button stopped the test...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Natus Neurology DBA Excel Tech., Ltd. (XLTEK)

Recalled Item: Natus Brain Monitor Breakout Box Recalled by Natus Neurology DBA Excel...

The Issue: Natus received two complaints of left side labeling show impedance for right...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Stryker Corporation

Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...

The Issue: Due to complaints their is the potential that irrigation solution may leaked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2025· Quidel Corporation

Recalled Item: QuickVue: Dipstick Strep A Test: 50T Recalled by Quidel Corporation Due to...

The Issue: Dipstick strep A test has potential for false positive results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2025· CARIS LIFE SCIENCES

Recalled Item: MI Cancer Seek UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Recalled...

The Issue: Due to an incorrect test results provided that indicated the incorrect drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2025· Intersurgical Inc

Recalled Item: i-view video laryngoscope. Model Number: 8008000. The i-view video...

The Issue: Potential for faulty devices as a result of depleted batteries.

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

Class I — Serious Health HazardOngoing
DrugJune 16, 2025· Qualgen, LLC

Recalled Item: Testosterone 200 mg Pellet packaged in 1mL amber vials Recalled by Qualgen,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date: A printing issue...

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

Class III — Low RiskOngoing
Refund
DrugJune 16, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund