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. 2,680 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,680 in last 12 months

Showing 2598126000 of 30,921 recalls

Medical DeviceJune 30, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo Imaging XS Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Siemens has become aware of the potential malfunction when using syngo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Ra Medical Systems Inc

Recalled Item: PHAROS Excimer Laser Recalled by Ra Medical Systems Inc Due to RA Medical...

The Issue: RA Medical Systems is recalling the PHAROS EX-308 Excimer Laser because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Steris Corporation

Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Product Usage: Usage: The...

The Issue: STERIS has identified that deformation of the washers door handle pin may...

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

Class III — Low RiskOngoing
Medical DeviceJune 27, 2014· Life Force of Tampa, LLC

Recalled Item: Life Force Chamber Product Usage:The product is intended for restful...

The Issue: The Life Force chamber is marketed and promoted as a medical device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2014· Steris Corporation

Recalled Item: The STERIS 4085 General Surgical Table Product Usage: is an Recalled by...

The Issue: STERIS engineering analysis has determined the D1 pressure switch in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2014· Brainlab AG

Recalled Item: Patient Data Manager 2.0 (Content manager 2.0 Recalled by Brainlab AG Due to...

The Issue: The following defects have been identified for data loaded with Patient Data...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2014· Integra LifeSciences Corp.

Recalled Item: Integra NewPort MIS System Model No. NWPIMP (NewPort Implant Tray Recalled...

The Issue: Integra LifeSciences is recalling the Integra NewPort MIS System because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2014· Biosound Esaote, Inc.

Recalled Item: Esaote PA230E Transducer A portable and cart base ultrasound system Recalled...

The Issue: Using the PA230E transducer with a user-defined setting with the output...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2014· Alphatec Spine, Inc.

Recalled Item: Solanas 2.1mm FIXED DEPTH DRILL Recalled by Alphatec Spine, Inc. Due to...

The Issue: Alphatec Spine is recalling the 2.1mm Fixed Depth Drill 10mm because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2014· Hill-Rom, Inc.

Recalled Item: Affinity¿ Four Birthing Bed Recalled by Hill-Rom, Inc. Due to The attachment...

The Issue: The attachment latch mechanism can become bent depending on user handling....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Peters Surgical

Recalled Item: The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a...

The Issue: A potential splitting of the surface treatment of the thread ends on certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Mckesson Information Solutions LLC

Recalled Item: McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete...

The Issue: McKesson Cardiology Hemo front-end parameter boxes must undergo annual...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Zimmer, Inc.

Recalled Item: Zimmer Dental Tapered Screw-Vent Implant Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Dental is conducting a voluntary recall of a single lot of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Salter Labs

Recalled Item: Oxygen Mask Recalled by Salter Labs Due to The case label correctly states...

The Issue: The case label correctly states partial rebreather but the insert label...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Peters Surgical

Recalled Item: The synthetic non-absorbable surgical sutures CARDIOFLON Evolution are...

The Issue: A potential splitting of the surface treatment of the thread ends on certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Dual-Release Folding Walker with 5" wheel Recalled by Owens &...

The Issue: Product wheels may be too loose, too tight, or fall off.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Concentric Medical Inc

Recalled Item: Merci Retriever Intended to restore blood flow in the neurovasculature...

The Issue: Merci Retrievers were shipped to US customers past their expiration date,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Karl Storz Endoscopy

Recalled Item: Essential NEO Recalled by Karl Storz Endoscopy Due to KARL STORZ...

The Issue: KARL STORZ Endoscopy-America is recalling the Essential NEO because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Biomet 3i, LLC

Recalled Item: BIOMET 3i Certain Bellatek Encode Healing Abutment Biomet 3i Healing...

The Issue: Identifiers on the label are correct but the label has the incorrect color...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Surgical System Console Recalled by Stryker Instruments...

The Issue: The firm received complaints regarding insufficient irrigation to the tip of...

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

Class II — Potential Health HazardOngoing