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. 1,877 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,877 in last 12 months

Showing 4110141120 of 55,713 recalls

DrugJuly 2, 2015· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...

The Issue: Presence of Particulate Matter and Lack of Assurance of Sterility: The firm...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2015· XTREME Z DISTRIBUTORS INC

Recalled Item: Zero Xtreme High Performance Fat Burner capsules Recalled by XTREME Z...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling and analysis confirmed...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI LXL CT/PET System. The Philips GEMINI PET/CT Imaging Systems Recalled...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Myoscience Inc

Recalled Item: iovera 155 Smart Tip Recalled by Myoscience Inc Due to The expiration date...

The Issue: The expiration date on the outer box label and the pouch label for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI GXL 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF 64 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Big Bore CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Base CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Ready CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
FoodJuly 1, 2015· Whole Food Market

Recalled Item: Peach Pie 9 Inch NET WT. 2lb 4oz (1021g) and Recalled by Whole Food Market...

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 1, 2015· Whole Food Market

Recalled Item: Blackberry Pie 9 Inch NET WT. 2lb 4oz (1021g) and Recalled by Whole Food...

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 1, 2015· Whole Food Market

Recalled Item: Cherry Pie 9 Inch NET WT. 2lb 4oz (1021g) and Recalled by Whole Food Market...

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 30, 2015· Michael Foods, Inc.

Recalled Item: Crystal Farms Simply Potatoes Shredded Hash Browns packaged as individual...

The Issue: Product may contain small slivers of shredded golf ball.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 30, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Processor EPX 2500 High Definition Endoscopy Recalled by Fujifilm...

The Issue: The EPX-2500 Operation Manual and sales brochure incorrectly identify that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· BIOTRONIK, Inc.

Recalled Item: PSW 1203.U/1 Recalled by BIOTRONIK, Inc. Due to Ventricular packing: LV...

The Issue: Ventricular packing: LV software programming versions for BIOTRONIK CRT-P...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Remel Inc

Recalled Item: PathoDx Strep Grouping Kit Recalled by Remel Inc Due to A reagent present...

The Issue: A reagent present may produce weak or slow reactions; continued use may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...

The Issue: Software anomaly may occur during the installation of an Assay Data Diskette...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Remel Inc

Recalled Item: PathoDx Strep B Grouping Latex Recalled by Remel Inc Due to A reagent...

The Issue: A reagent present may produce weak or slow reactions; continued use may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: in case a system error occurs and the system enters the "Bypass Fluoro" mode...

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

Class II — Potential Health HazardOngoing