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. 2,585 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,585 in last 12 months

Showing 5250152520 of 55,713 recalls

Medical DeviceFebruary 7, 2013· Smith & Nephew Inc

Recalled Item: INTERNAL HEX RECON SCREW Recalled by Smith & Nephew Inc Due to 75 mm screws...

The Issue: 75 mm screws were packaged and labeled using an 80 mm screw outer box and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2013· Smith & Nephew Inc

Recalled Item: INTERNAL HEX RECON SCREW Recalled by Smith & Nephew Inc Due to 75 mm screws...

The Issue: 75 mm screws were packaged and labeled using an 80 mm screw outer box and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+ Hyperbaric Infusion Pump. List Number 11005. The Plum Recalled by...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+3 Infusion Pump. List Number 12618. The Plum A+ Recalled by Hospira...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump. List Number 11971. The Plum A+ Recalled by Hospira...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump with Hospira MedNet Software. List Number Recalled by...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+3 Infusion Pump with Hospira MedNet Software. List Number Recalled by...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+3 Infusion Pump. List Number 12391. The Plum A+ Recalled by Hospira...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump. List Number 11973. The Plum A+ Recalled by Hospira...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+3 Infusion Pump System. List Number 12348. The Plum Recalled by...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump with Hospira MedNet Software. List Number Recalled by...

The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Heritage Labs International LLC

Recalled Item: Heritage Labs Path Study Extra Supplies Kit Recalled by Heritage Labs...

The Issue: The product has a Lithium Heparin contaminant which could adversely affect...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2013· Smiths Medical ASD, Inc.

Recalled Item: Smiths Medical Recalled by Smiths Medical ASD, Inc. Due to In rare...

The Issue: In rare instances, the BCI¿ Remote Alarm Cables (BCI¿ Cable) are not...

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

Class I — Serious Health HazardOngoing
FoodFebruary 5, 2013· Buffalo Trace Distillery

Recalled Item: BUFFALO TRACE BOURBON FLAVORED CARAMEL SAUCE 8 oz glass jars Recalled by...

The Issue: The firm failed to include allergen milk on the label of this sauce.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2013· Buffalo Trace Distillery

Recalled Item: BUFFALO TRACE MARINADE FOR MEAT Net Wt. 12 fl. oz. Recalled by Buffalo Trace...

The Issue: The firm failed to include allergens of wheat and anchovy on the label of...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2013· Buffalo Trace Distillery

Recalled Item: BUFFALO TRACE BOURBON FUDGE SAUCE 8 oz glass jars Net Wt. 8 fl. oz./227 g...

The Issue: The firm failed to include allergens of milk and soy on the label of this sauce.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2013· Buffalo Trace Distillery

Recalled Item: BUFFALO TRACE HOT BARBEQUE SAUCE Net Wt. 16 fl. oz./532 Recalled by Buffalo...

The Issue: The firm failed to include allergens of soy and anchovy on the labels of...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2013· Buffalo Trace Distillery

Recalled Item: BUFFALO TRACE ORIGINAL FLAVOR BARBEQUE SAUCE Net Wt. 16 fl. Recalled by...

The Issue: The firm failed to include allergens of soy and anchovy on the label of this...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 5, 2013· Zimmer Biomet, Inc.

Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...

The Issue: Observed instability of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2013· Hospira Inc.

Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to Hospira has...

The Issue: Hospira has received reports of Malfunction S205 Backup Battery Failure...

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

Class II — Potential Health HazardOngoing