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. 1,947 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,947 in last 12 months

Showing 3316133180 of 55,713 recalls

Medical DeviceMarch 13, 2017· Nihon Kohden America Inc

Recalled Item: Bedside monitor CSM-1901(Life Scope G9) with main unit CU-192RA. The...

The Issue: The Pause function on central monitors will not automatically resume when...

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

Class II — Potential Health HazardOngoing
DrugMarch 12, 2017· Meridian Medical Technologies a Pfizer Company

Recalled Item: EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg Recalled by Meridian...

The Issue: Defective Delivery System; reports of the device failing to activate which...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 12, 2017· Meridian Medical Technologies a Pfizer Company

Recalled Item: EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg Recalled by Meridian...

The Issue: Defective Delivery System; reports of the device failing to activate which...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 11, 2017· McShare's Inc

Recalled Item: iXL Advanced Performance Matrix Recalled by McShare's Inc Due to Product...

The Issue: Product manufactured with an ingredient that contains low levels of soy; soy...

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

Class III — Low RiskOngoing
Refund
FoodMarch 11, 2017· McShare's Inc

Recalled Item: Premark HS Vitamin RDA Premix Recalled by McShare's Inc Due to Product...

The Issue: Product manufactured with an ingredient that contains low levels of soy; soy...

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

Class III — Low RiskOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Fluconazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Claris Lifesciences Inc...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Metronidazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 10, 2017· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is...

The Issue: Product shipped proximate to or past the expiration date listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2017· Heartware

Recalled Item: HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product...

The Issue: In April 2015, HeartWare, now a part of Medtronic, notified users of a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW Recalled by Smith &...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Cincinnati Sub-Zero Products Inc

Recalled Item: Hemotherm CE Recalled by Cincinnati Sub-Zero Products Inc Due to Improperly...

The Issue: Improperly rated fuses were used in the manufacture of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· C.R. Bard, Inc.

Recalled Item: SURESTEP Tray Recalled by C.R. Bard, Inc. Due to Misbranded: Product...

The Issue: Misbranded: Product labeled, Not made with natural rubber latex, may in...

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

Class II — Potential Health HazardOngoing
DrugMarch 8, 2017· Mckesson Medical Surgical

Recalled Item: hydrALAZINE HYDROCHLORIDE INJECTION Recalled by Mckesson Medical Surgical...

The Issue: Temperature Abuse: Certain pieces of these lots distributed by McKesson...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Triamcinolone 40 mg/mL 2 mL Single-Dose Vial for Injection Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 8, 2017· Gerber Products Company dba Nestle Infant Nutrition

Recalled Item: Gerber¿ Pasta Pick-Ups Cheese Ravioli Net Wt 6 oz (170g) Recalled by Gerber...

The Issue: Gerber Products Company is recalling Cheese Ravioli Gerber¿ Pasta Pick-Ups¿...

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

Class II — Potential Health HazardOngoing
Refund