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.
Showing 25921–25940 of 30,921 recalls
Recalled Item: Tibila Insert CK Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ascenda Intrathecal Catheter models 8780 and 8781 Recalled by...
The Issue: Medtronic is removing specific lots of the Ascenda Intrathecal Catheters and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management....
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowCOUPLER. An implantable device that is used to detect blood Recalled by...
The Issue: Baxter Healthcare is recalling the FlowCOUPLER Device because there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Post-Op Surgical Kits . Kit includes: Amerigel Wound Dressing...
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibila Insert UC Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS Tibial Insert Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pivot Bipolar Cup 22x42/43-51/53mm Recalled by Ortho Development Corporation...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Foley Urinary Catheter Insertion Tray with 10cc syringe Recalled by...
The Issue: Labeling error: The manufacturing date is the same as the expiration date....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table with Dual 2 Way Drop Section...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Hulka Clip is a sterile packaged medical device that Recalled by Richard...
The Issue: Richard Wolf Medical Instrument Corporation is recalling Hulka Clip Tubal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kodak DirectView DR 7500 Diagnostic X-Ray System Product Usage: The Recalled...
The Issue: An on-site evaluation of the equipment parts that attach the Beta Assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...
The Issue: The temperature probe does not properly connect to the temperature port.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene BC-GN Test Kit (Catalog number 20-005-021) includes: 1) 20 Recalled...
The Issue: Nanosphere Inc. has recently determined through four customer complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...
The Issue: The temperature probe does not properly connect to the temperature port.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emerald Fiberoptic Blade Recalled by Teleflex Medical Due to Packaging...
The Issue: Packaging Error: Customers have reported receiving incorrect product. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Falope-Ring Dilator Recalled by Gyrus Medical, Inc Due to...
The Issue: Falope-Ring Dilator for Reusable Falope-Ring Band Applicators have been sold...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.