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. 2,680 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,680 in last 12 months

Showing 2880128820 of 55,713 recalls

FoodMarch 14, 2018· GRIFFITH FOODS

Recalled Item: Product Name Lot Number or ID Pan Roast Brown Gravy Mix 659281 Recalled by...

The Issue: Griffith Foods, Inc. has initiated a voluntary recall of multiple products...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2018· GRIFFITH FOODS

Recalled Item: Product Name Lot Number or ID Toasted Italian Herbs 661126 Recalled by...

The Issue: Griffith Foods, Inc. has initiated a voluntary recall of multiple products...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2018· Vietti Acquisitions, LLC

Recalled Item: Southgate Hot Dog Chili Sauce 15 oz cans Recalled by Vietti Acquisitions,...

The Issue: The firm was notified by a customer that the product contains Dumplings with...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 14, 2018· Philips Electronics North America Corp.

Recalled Item: Philips HeartStart FRx AED. Recalled by Philips Electronics North America...

The Issue: An issue with one of the electric components (a resistor) could result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect simply InterActive Implant Recalled by Implant Direct Sybron...

The Issue: The cap on the vial might be labeled with the incorrect part number but the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Philips Electronics North America Corp.

Recalled Item: Philips HeartStart (HS1) Onsite/Home AED Recalled by Philips Electronics...

The Issue: An issue with one of the electric components (a resistor) could result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Invivo Corporation

Recalled Item: PHILIPS Xper Flex Cardio Physiomonitoring System Recalled by Invivo...

The Issue: The real-time numeric value for ventricular end-diastolic pressure (EDP)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision Recalled by...

The Issue: After continuous operation for more than one and a half days, the image on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Accelerate Diagnostics Inc

Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...

The Issue: The kits may produce an elevated rate of false positive calls for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· BioFire Diagnostics, LLC

Recalled Item: FilmArray BCID Panel (Blood Culture Identification Panel) Recalled by...

The Issue: There is an increased risk of false positive Proteus results when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2018· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Prestige LP(TM) Cervical Disc System with Streamlined Instruments...

The Issue: The firm received complaints of drill bits breaking during use with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2018· Keystone Dental Inc

Recalled Item: Genesis Surgical Cassette Tapered Implants are intended for placement...

The Issue: The surgical cassette contained extra-large white grommets making the 3.8 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· McKesson Israel Ltd.

Recalled Item: McKesson Cardiology Hemo Recalled by McKesson Israel Ltd. Due to Change...

The Issue: Change Healthcare has identified an issue where, under certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Ohio Medical Corporation

Recalled Item: Vacuum Regulator Recalled by Ohio Medical Corporation Due to Final quality...

The Issue: Final quality control testing was not completed before the devices were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Hamilton Medical AG

Recalled Item: Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults...

The Issue: After two and a half years, the battery fuel gauge may indicate a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva¿ EMIT¿ II Plus 6-Acetyl morphine Catalog # for 28 Recalled by Siemens...

The Issue: Incorrect calibrator level listed in qualitative calibration steps

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

Class III — Low RiskOngoing
Medical DeviceMarch 12, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva¿ EMIT¿ II Plus 6-Acetylmorphine Catalog # for 1000 mL: Recalled by...

The Issue: Incorrect calibrator level listed in qualitative calibration steps

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

Class III — Low RiskOngoing
Medical DeviceMarch 12, 2018· CooperSurgical, Inc.

Recalled Item: 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length...

The Issue: Products have been packaged with the wrong Trocar length type.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker GmbH

Recalled Item: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation...

The Issue: The wrong parts were picked for packaging. The connecting Nuts were packed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...

The Issue: The power load floor plates which hold the ambulance cot anchors in place...

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

Class II — Potential Health HazardOngoing