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. 1,049 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,049 in last 12 months

Showing 30601–30620 of 55,713 recalls

Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
FoodAugust 7, 2017· Mary's Gone Crackers, Inc.

Recalled Item: Mary's Gone Crackers Original Crackers: Organic Recalled by Mary's Gone...

The Issue: Recall of crackers due to pieces of blue grade plastic liner found inside...

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

Class III — Low RiskOngoing
Refund
DrugAugust 7, 2017· International Laboratories, Inc.

Recalled Item: Pravastatin Sodium Tablets Recalled by International Laboratories, Inc. Due...

The Issue: Labeling: Label mix-up, the product labeled as Pravastatin sodium tablets 40...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Stemmed Tibial Provisional Size H Right Recalled by Zimmer Biomet,...

The Issue: There is a potential for intermittent cracks in the raw material batch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Cemented Tibial SZ PLT Size H Right Recalled by Zimmer Biomet, Inc....

The Issue: There is a potential for intermittent cracks in the raw material batch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Merge Healthcare, Inc.

Recalled Item: Merge Unity software Recalled by Merge Healthcare, Inc. Due to The software...

The Issue: The software is not identifying the patient as having atypical hyperplasia,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Stemmed Tibial Provisional Size H Left Recalled by Zimmer Biomet,...

The Issue: There is a potential for intermittent cracks in the raw material batch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Cemented Tibial SZ PLT Size H Left Recalled by Zimmer Biomet, Inc....

The Issue: There is a potential for intermittent cracks in the raw material batch used...

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

Class II — Potential Health HazardOngoing
DrugAugust 4, 2017· Pfizer Inc.

Recalled Item: Quillivant XR methylphenidate HCl Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2017· Pfizer Inc.

Recalled Item: Quillivant XR methylphenidate HCl Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 4, 2017· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...

The Issue: The barcode label was placed underneath the sterile barrier and the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2017· ZOLL Medical Corporation

Recalled Item: OneStep CPR Complete Recalled by ZOLL Medical Corporation Due to A portion...

The Issue: A portion of one lot of ZOLL OneStep Complete Electrodes for adults will...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2017· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...

The Issue: The barcode label was placed underneath the sterile barrier and the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2017· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...

The Issue: The barcode label was placed underneath the sterile barrier and the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2017· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...

The Issue: The barcode label was placed underneath the sterile barrier and the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2017· Ultradent Products, Inc.

Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...

The Issue: The barcode label was placed underneath the sterile barrier and the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2017· OrthoPediatrics Corp

Recalled Item: Response 5.5/6.0 Spine System 7.0mm x 40mm Pedicle Screw Product Recalled by...

The Issue: The 7mm diameter uniaxial pedicle screws have been color anodized with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2017· Gyrus ACMI, Inc.

Recalled Item: Gyrus ACMI Round Cutting Burrs - to be used with the Diego Elite system...

The Issue: "Chattering" when cutting burrs are used in bone.

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

Class II — Potential Health HazardOngoing
DrugAugust 3, 2017· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Lorazepam Oral Concentrate Recalled by Amneal Pharmaceuticals of New York,...

The Issue: Defective Delivery System: the dropper measurement markings may be reversed,...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 3, 2017· KVK-Tech, Inc.

Recalled Item: Phentermine HCL Capsules Recalled by KVK-Tech, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: out-of-specification results...

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

Class III — Low RiskOngoing
Refund