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. 2,677 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,677 in last 12 months

Showing 3090130920 of 55,713 recalls

FoodJuly 5, 2017· Clif Bar & Company

Recalled Item: Clif Kid Zbar Protein Chocolate Mint 10-pack Recalled by Clif Bar & Company...

The Issue: Undeclared peanuts and/or tree nuts.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2017· Clif Bar & Company

Recalled Item: Clif Builders Variety Pack Chocolate Peanut Butter and Chocolate Mint...

The Issue: Undeclared peanuts and/or tree nuts.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2017· Clif Bar & Company

Recalled Item: Clif Kid Zbar Protein Variety Pack 30-count Recalled by Clif Bar & Company...

The Issue: Undeclared peanuts and/or tree nuts.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2017· Raja Foods, L.L.C.

Recalled Item: Anarkali Peshawari Naan Bread Frozen 15oz. retail plastic pouch 24 Recalled...

The Issue: Undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 5, 2017· Cosman Medical, LLC

Recalled Item: Nitinol TC Reusable Electrodes (TCN) Recalled by Cosman Medical, LLC Due to...

The Issue: After multiple reprocessing cycles, the epoxy resin which holds the TCN...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Roche Diagnostics Corporation

Recalled Item: cobas e 411 Immunoassay Analyzer-Model/Catalog/Part number:...

The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Roche Diagnostics Corporation

Recalled Item: Roche / Hitachi MODULAR Analyzer Systems-Immunoassay...

The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Phadia US Inc

Recalled Item: Phadia 1000 Instrument Recalled by Phadia US Inc Due to The "Retry" command...

The Issue: The "Retry" command does not function properly which could cause a shortage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Partial Knee System Recalled by Zimmer Biomet, Inc. Due to Finishing...

The Issue: Finishing guide does not adequately account for shape differences present in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Novo Nordisk Inc

Recalled Item: Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product...

The Issue: A small number of batches may crack or break if exposed to certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2017· Teleflex Medical

Recalled Item: LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600...

The Issue: Teleflex Medical is recalling the affected product because there may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2017· Stanmore Implants Worldwide Ltd.

Recalled Item: JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur Recalled...

The Issue: Three (3) complaints were identified in which the potential for utilization...

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

Class II — Potential Health HazardOngoing
FoodJuly 3, 2017· Nisbet Oyster Co Inc

Recalled Item: Steamers in 5 Clams in Butter & Garlic Sauce Recalled by Nisbet Oyster Co...

The Issue: Undeclared milk. Goose Point Steamers in 5 Clams in Butter & Garlic Sauce is...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 3, 2017· Trinidad Benham Corp

Recalled Item: HY-TOP Rice MIX CHICKEN FLAVORED RICE & VERMICELLI WITH SEASONINGS Recalled...

The Issue: The firm failed to declare wheat in the ingredient statement.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 3, 2017· Avid Medical, Inc.

Recalled Item: AVID Medical QA Pack AV10654-10 Recalled by Avid Medical, Inc. Due to The...

The Issue: The swab stick collection device provided in a convenience kit expires prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· R82 A/S

Recalled Item: Heron toilet and bath chair Model 880505-01 & 880505-11 Recalled by R82 A/S...

The Issue: Replacement campaign on all units that have a gas spring head in aluminum.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Elekta, Inc.

Recalled Item: MOSAIQ Medical Charged-Particle Radiation Therapy System Recalled by Elekta,...

The Issue: The table shift in the vertical direction was inverted during the use of CMA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Alcon Research, Ltd.

Recalled Item: ORA System with VerifEye+ Cart Recalled by Alcon Research, Ltd. Due to Some...

The Issue: Some ORA Carts have the potential to return an incorrect IOL power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Alcon Research, Ltd.

Recalled Item: ORA System with VerifEye Recalled by Alcon Research, Ltd. Due to Some ORA...

The Issue: Some ORA Carts have the potential to return an incorrect IOL power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· CareFusion 303, Inc.

Recalled Item: VersaSafe Plastic Cannula - 11 Gauge Recalled by CareFusion 303, Inc. Due to...

The Issue: Punctures in blister packaging that was detected during the packaging process.

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

Class II — Potential Health HazardOngoing