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 2862128640 of 30,921 recalls

Medical DeviceApril 30, 2013· Angiodynamics, Inc.

Recalled Item: AngioDynamics Micro Introducer Kits under the following labeling: 1)...

The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Elekta, Inc.

Recalled Item: Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated...

The Issue: Unexpected movement during beam delivery may not be detected if there are...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar 360. Designed to meet the needs for lifting humans. Recalled by...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar Standard. Designed to meet the needs for lifting humans. Recalled...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Angiodynamics, Inc.

Recalled Item: AngioDynamics VenaCure EVLT NeverTouch-FRS PROCEDURE KIT under the following...

The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· TZ Medical Inc.

Recalled Item: adult defibrillation Recalled by TZ Medical Inc. Due to TZ Medical Inc is...

The Issue: TZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· American Optisurgical Inc

Recalled Item: FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray....

The Issue: American Optisurgical, Inc initiated a recall of ChloraPrep Hi-Lite Orange...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: EZ Breathe Atomizer Model # EZ-100. For the delivery of Recalled by Nephron...

The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar 350. Designed to meet the needs for lifting humans. Recalled by...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar Wide 670. Designed to meet the needs for lifting humans. Recalled...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2013· Biomet, Inc.

Recalled Item: Biomet Trauma Phoenix Retrograde Femoral Connecting Bolt Trauma Fixation...

The Issue: Biomet Trauma ("Biomet") has initiated a recall of Retrograde Femoral...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Heart Sync, Inc

Recalled Item: Heart Sync C100-Physio Radiotransparent Defibrillation Electrodes Monophasic...

The Issue: On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Heart Sync, Inc

Recalled Item: Vermed Recalled by Heart Sync, Inc Due to On 4/18/13 HEARTSYNC became aware...

The Issue: On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Cardio Medical Products

Recalled Item: Cardio Medical Products Recalled by Cardio Medical Products Due to Covidien...

The Issue: Covidien received customer reports of Arcing/Sparking on the defibrillation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Beckman Coulter Inc.

Recalled Item: AU2700 Clinical Chemistry Analyzer AU5400 Clinical Chemistry Analyzer...

The Issue: Beckman Coulter is recalling AU2700/AU2700 Plus & AU5400 Clinical Chemistry...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is...

The Issue: Siemens has confirmed that the TACR method may demonstrate reduced on-board...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******iMRI Handpiece. Use with iMRI System Only***Rx Only***Manufacturer:...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· SpineFrontier, Inc.

Recalled Item: S-LIFT Slap Hammer Recalled by SpineFrontier, Inc. Due to Malfunction of...

The Issue: Malfunction of slap hammer.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Leibel-Flarsheim Company LLC

Recalled Item: Hydra Vision DR 60/80 System Recalled by Leibel-Flarsheim Company LLC Due to...

The Issue: A complaint was received in which a hospital physicist indicated the dosage...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: B-CrossLaps/serum (B-CTx in serum) 160 100 tests Immunoassay Recalled by...

The Issue: Roche Diagnostics internal investigations in R&D have shown that the claims...

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

Class II — Potential Health HazardOngoing