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. 2,692 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,692 in last 12 months

Showing 2488124900 of 55,713 recalls

Medical DeviceMarch 1, 2019· Integra Limited

Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...

The Issue: Temperature indicator may have changed color to dark gray or black prior to...

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

Class II — Potential Health HazardOngoing
FoodMarch 1, 2019· Lamb Weston Inc

Recalled Item: Lamb's Supreme Starz Recalled by Lamb Weston Inc Due to Foreign Object...

The Issue: Lamb's Supreme Starz (Star-shaped Hash Brown Patties) are recalled due to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 28, 2019· Fungi Perfecti LLC

Recalled Item: Host Defense MycoBotanicals Blood Sugar Recalled by Fungi Perfecti LLC Due...

The Issue: Host Defense MycoBotanicals Blood Sugar, 60 ct. bottles, is recalled due to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 28, 2019· Philips North America, LLC

Recalled Item: Urodiagnost Recalled by Philips North America, LLC Due to The locking plate...

The Issue: The locking plate may be missing from the system, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet Small Diameter Cement Plug Inserter-Sterile Recalled by Zimmer...

The Issue: Lack of an adequate sterilization validation

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2019· Philips North America, LLC

Recalled Item: MultiDiagnost Eleva w/ Flat Detector Recalled by Philips North America, LLC...

The Issue: The locking plate may be missing from the system, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2019· Becton Dickinson & Company

Recalled Item: SmartSite Syringe Administration Set-Product Package Size 50 Recalled by...

The Issue: Leaking of the Smartsite Syringe Administration Set. May result in delay or...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 28, 2019· Philips North America, LLC

Recalled Item: Omnidiagnost Classic Recalled by Philips North America, LLC Due to The...

The Issue: The locking plate may be missing from the system, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2019· Philips North America, LLC

Recalled Item: MultiDiagnost-Eleva Recalled by Philips North America, LLC Due to The...

The Issue: The locking plate may be missing from the system, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2019· Philips North America, LLC

Recalled Item: URODiagnost Eleva Recalled by Philips North America, LLC Due to The locking...

The Issue: The locking plate may be missing from the system, which may result in...

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

Class II — Potential Health HazardOngoing
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Camber Pharmaceuticals Inc

Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Camber Pharmaceuticals Inc

Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Camber Pharmaceuticals Inc

Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2019· Teleflex Medical

Recalled Item: Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape...

The Issue: The device label incorrectly states that the device is sterile. This product...

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

Class III — Low RiskOngoing