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. 2,708 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,708 in last 12 months

Showing 2194121960 of 55,713 recalls

Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: FEMOROTIBIAL/FEMORAL NAIL Recalled by Zimmer Biomet, Inc. Due to Non-highly...

The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: CLS Brevius Stem Kinectiv Recalled by Zimmer Biomet, Inc. Due to Non-highly...

The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Various Hip Joint Replacement Systems Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: CABLE-READY SHORT GTR and CABLE-READY LONG GTR Recalled by Zimmer Biomet,...

The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: NCB Proximal Lateral Tibia Recalled by Zimmer Biomet, Inc. Due to Non-highly...

The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Various Custom Devices Recalled by Zimmer Biomet, Inc. Due to Non-highly...

The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...

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

Class II — Potential Health HazardOngoing
DrugOctober 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Chorionic Gonadotropin 11 Recalled by Innoveix Pharmaceuticals...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Human Chorionic Gonadotropin 5 Recalled by Innoveix...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Human Chorionic Gonadotropin 5 Recalled by Innoveix...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Sermorelin w/ GHRP2 3 mg For injection Recalled by Innoveix...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2019· Dollar General Corporation

Recalled Item: Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar Recalled by...

The Issue: Possible undeclared milk allergen in product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 10, 2019· Trilliant Surgical, LLC

Recalled Item: 3.5mm Aresenal Screw Drill Bit Recalled by Trilliant Surgical, LLC Due to...

The Issue: Labeling Error; specifically, drill bits from lots # TSL008495A are marked...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Hologic, Inc

Recalled Item: Panther Fusion Extraction Reagent-S Recalled by Hologic, Inc Due to Reagent...

The Issue: Reagent component included in flu test kit may cause both high background...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Biocare Medical, LLC

Recalled Item: 4plus Streptavidin HRP Label Recalled by Biocare Medical, LLC Due to Firm...

The Issue: Firm has identified product has no staining. If used, may result in invalid...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators Endo Smartcap Endoscope Tubing. . Packaged as Contents 1 Recalled...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Stryker Sustainability Solutions

Recalled Item: Zimmer Tourniquet Cuff 30" (Blue) Recalled by Stryker Sustainability...

The Issue: Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators Endo carry-on Procedure Kit - Product Usage: Recalled by...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators EndoGator . Kit for Olympus 140/160/180/190 Series GI Recalled by...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing