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 2200122020 of 55,713 recalls

Medical DeviceOctober 4, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Homocysteine-In vitro test for the quantitative determination of total...

The Issue: Homocysteine Reagent, Calibration Failures and Quality Control Recovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...

The Issue: Communication error alarms may result in interruption of therapy, delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...

The Issue: Communication error alarms may result in interruption of therapy, delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...

The Issue: Communication error alarms may result in interruption of therapy, delay in...

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

Class II — Potential Health HazardOngoing
DrugOctober 4, 2019· KVK-Tech, Inc.

Recalled Item: Methylphenidate Hydrochloride Oral Solution 5mg per 5mL Recalled by...

The Issue: Presence of Foreign Substance; Fiber particles.

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 3, 2019· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 440mm shaft Recalled by...

The Issue: The staplers may contain an out of specification anvil component within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 3, 2019· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft Recalled by Ethicon...

The Issue: The staplers may contain an out of specification anvil component within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 3, 2019· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 340mm shaft Recalled by...

The Issue: The staplers may contain an out of specification anvil component within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 3, 2019· Philips North America, LLC

Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...

The Issue: Device may fail to turn on or unexpectedly attempt to restart, rendering it...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2019· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 280mm shaft Recalled by...

The Issue: The staplers may contain an out of specification anvil component within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 3, 2019· Datascope Corp.

Recalled Item: Low Level Output Cable Interface to Philips Monitor For Use Recalled by...

The Issue: One lot of "Low Level Output Cable - Interface to Philips Monitor" was...

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

Class II — Potential Health HazardOngoing
FoodOctober 3, 2019· Arcadia Trading Inc.

Recalled Item: Dried Mushroom NET WT: 8oz (227g) Ingredients: Mushroom Distributed By:...

The Issue: Product contains undeclared sulfites.

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 2, 2019· Pega Medical Inc.

Recalled Item: SCFE (slipped capital femoral epiphysis) Knobs for Driver Recalled by Pega...

The Issue: There is a potential for the screws to have become loosened during...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2019· Exactech, Inc.

Recalled Item: 2.4mm x 2.5 Fluted Pin Pouch Recalled by Exactech, Inc. Due to Potential for...

The Issue: Potential for the 2.4mm x 2.5 Fluted Pin Pouch to contain a single pin...

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

Class II — Potential Health HazardOngoing
DrugOctober 2, 2019· Pfizer Inc.

Recalled Item: 10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection Recalled...

The Issue: Lack of Assurance of Sterility: Bag has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 2, 2019· Zeiss, Carl Inc

Recalled Item: Component for Laser Scanning Microscopes (LSM 700 Recalled by Zeiss, Carl...

The Issue: When the user tilts the transmitted light arm of the microscope to the end...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Groshong 9.5 Dual-Lumen CV Catheter Recalled by Bard Peripheral Vascular...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs Recalled...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. X-Port isp M.R.I Implantable Port Recalled by Bard Peripheral Vascular...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing